Marie-geneviève Mattéi
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(Suggest an Edit or Addition)Marie-geneviève Mattéi's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A new member of the immunoglobulin superfamily—CTLA-4 (1987) (1135)
- CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene. (1993) (767)
- Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes (1991) (659)
- CTLA-4 and CD28 activated lymphocyte molecules are closely related in both mouse and human as to sequence, message expression, gene structure, and chromosomal location. (1991) (439)
- A novel lysosome-associated membrane glycoprotein, DC-LAMP, induced upon DC maturation, is transiently expressed in MHC class II compartment. (1998) (422)
- Cloning and primary sequence of a mouse candidate prohormone convertase PC1 homologous to PC2, Furin, and Kex2: distinct chromosomal localization and messenger RNA distribution in brain and pituitary compared to PC2. (1991) (421)
- A New Member of the Rho Family, Rnd1, Promotes Disassembly of Actin Filament Structures and Loss of Cell Adhesion (1998) (383)
- The chemokine TECK is expressed by thymic and intestinal epithelial cells and attracts double‐ and single‐positive thymocytes expressing the TECK receptor CCR9 (2000) (380)
- Isolation of a YAC clone covering a cluster of nine S100 genes on human chromosome 1q21: rationale for a new nomenclature of the S100 calcium-binding protein family. (1995) (351)
- A Novel, Secreted Form of Human ADAM 12 (Meltrin α) Provokes Myogenesis in Vivo * (1998) (347)
- A novel putative receptor protein tyrosine kinase of the met family. (1993) (341)
- A mouse model for hereditary thyroid dysgenesis and cleft palate (1998) (324)
- Human Ig superfamily CTLA‐4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA‐4 cytoplasmic domains (1988) (308)
- Regional expression of the homeobox gene Nkx-2.2 in the developing mammalian forebrain (1992) (298)
- Characterization of the HST-related FGF.6 gene, a new member of the fibroblast growth factor gene family. (1989) (279)
- Cloning of two novel ABC transporters mapping on human chromosome 9. (1994) (274)
- Cloning, Chromosomal Mapping, and Expression of a Novel Human Secretory Phospholipase A2 * (1997) (272)
- Identification of four novel human genes amplified and overexpressed in breast carcinoma and localized to the q11-q21.3 region of chromosome 17. (1995) (266)
- Identification and Characterization of a Novel Human Matrix Metalloproteinase with Unique Structural Characteristics, Chromosomal Location, and Tissue Distribution* (1997) (264)
- The mouse neuronal cell surface protein F3: a phosphatidylinositol- anchored member of the immunoglobulin superfamily related to chicken contactin (1989) (262)
- SRPX2 mutations in disorders of language cortex and cognition. (2006) (253)
- Identification and Characterization of a Novel Siglec, Siglec-7, Expressed by Human Natural Killer Cells and Monocytes* (1999) (238)
- Insensitivity to anti–Müllerian hormone due to a mutation in the human anti–Müllerian hormone receptor (1995) (235)
- The lung amiloride-sensitive Na+ channel: biophysical properties, pharmacology, ontogenesis, and molecular cloning. (1994) (234)
- Cloning of the cDNA encoding human tissue inhibitor of metalloproteinases-3 (TIMP-3) and mapping of the TIMP3 gene to chromosome 22. (1994) (231)
- Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex. (1993) (228)
- Organization of the Gene Encoding the Human Endothelin-converting Enzyme (ECE-1) (*) (1995) (221)
- Structure, mapping, and expression of fisp-12, a growth factor-inducible gene encoding a secreted cysteine-rich protein. (1991) (216)
- Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localization. (1993) (209)
- The Human 180-kDa Receptor for Secretory Phospholipases A2 (1995) (208)
- kappa-Opioid receptor in humans: cDNA and genomic cloning, chromosomal assignment, functional expression, pharmacology, and expression pattern in the central nervous system. (1995) (207)
- Mapping of the gene for anti-müllerian hormone to the short arm of human chromosome 19. (1987) (202)
- Human type VII collagen: cDNA cloning and chromosomal mapping of the gene. (1991) (200)
- Structure, mapping, and expression of erp, a growth factor-inducible gene encoding a nontransmembrane protein tyrosine phosphatase, and effect of ERP on cell growth (1993) (192)
- Identification and Characterization of a Widely Expressed Form of Adenylyl Cyclase* (1996) (192)
- Early expression of AMH in chicken embryonic gonads precedes testicular SOX9 expression (1998) (186)
- The inducible cytotoxic T-lymphocyte-associated gene transcript CTLA-1 sequence and gene localization to mouse chromosome 14 (1986) (183)
- Six S100 genes are clustered on human chromosome 1q21: identification of two genes coding for the two previously unreported calcium-binding proteins S100D and S100E. (1993) (179)
- Identification of Mouse Langerin/CD207 in Langerhans Cells and Some Dendritic Cells of Lymphoid Tissues1 (2002) (178)
- Family of Ebf/Olf‐1‐related genes potentially involved in neuronal differentiation and regional specification in the central nervous system (1997) (177)
- Gene Structure, Expression Pattern, and Biological Activity of Mouse Killer Cell Activating Receptor-associated Protein (KARAP)/DAP-12* (1998) (171)
- SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signalling. (2001) (170)
- Characterization of Spi-B, a transcription factor related to the putative oncoprotein Spi-1/PU.1 (1992) (167)
- Barx1, a new mouse homeodomain transcription factor expressed in cranio-facial ectomesenchyme and the stomach (1995) (161)
- A T‐cell specific TCR delta DNA binding protein is a member of the human GATA family. (1991) (161)
- Mouse Lbx1 and human LBX1 define a novel mammalian homeo☐ gene family related to the Drosophila lady bird genes (1995) (160)
- Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male (1983) (156)
- Kidd Blood Group and Urea Transport Function of Human Erythrocytes Are Carried by the Same Protein (*) (1995) (154)
- The putative oncogene Spi-1: murine chromosomal localization and transcriptional activation in murine acute erythroleukemias. (1989) (147)
- TIF1γ, a novel member of the transcriptional intermediary factor 1 family (1999) (144)
- Structure, chromosome location, and expression of the mouse zinc finger gene Krox-20: multiple gene products and coregulation with the proto-oncogene c-fos (1989) (143)
- Kv8.1, a new neuronal potassium channel subunit with specific inhibitory properties towards Shab and Shaw channels. (1996) (142)
- The del22q11.2 Candidate Gene Tbx1 Controls Regional Outflow Tract Identity and Coronary Artery Patterning (2008) (140)
- The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice (1986) (140)
- Characterization of cDNAs encoding human leukosialin and localization of the leukosialin gene to chromosome 16. (1989) (140)
- Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP‐3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10 (1994) (137)
- Hox-5.1 defines a homeobox-containing gene locus on mouse chromosome 2. (1988) (135)
- Several receptor tyrosine kinase genes of the Eph family are segmentally expressed in the developing hindbrain (1994) (132)
- Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency (1996) (131)
- Human uncoupling protein gene: Structure, comparison with rat gene, and assignment to the long arm of chromosome 4 (1990) (130)
- Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen. (1988) (128)
- Cloning and characterization of human type 2 and type 3 inositol 1,4,5-trisphosphate receptors. (1994) (128)
- Subtractive cloning and characterization of DRAL, a novel LIM-domain protein down-regulated in rhabdomyosarcoma. (1997) (128)
- Characterization of the murine Mpl proto-oncogene, a member of the hematopoietic cytokine receptor family: molecular cloning, chromosomal location and evidence for a function in cell growth. (1993) (128)
- Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations (2003) (126)
- Structure and Expression of Human Fibroblast Growth Factor-10* (1997) (124)
- Localization of the human NCAM gene to band q23 of chromosome 11: the third gene coding for a cell interaction molecule mapped to the distal portion of the long arm of chromosome 11 (1986) (122)
- TFEC, a basic helix-loop-helix protein, forms heterodimers with TFE3 and inhibits TFE3-dependent transcription activation (1993) (120)
- Cloning, functional expression, and regulation of two K+ channels in human T lymphocytes. (1992) (120)
- Chromosomal localization of the hst oncogene and its co-amplification with the int.2 oncogene in a human melanoma. (1988) (120)
- Zinedin, SG2NA, and Striatin Are Calmodulin-binding, WD Repeat Proteins Principally Expressed in the Brain* (2000) (116)
- Identification, characterization and leucocyte expression of Siglec-10, a novel human sialic acid-binding receptor. (2001) (113)
- Molecular characterization of a new urea transporter in the human kidney (1996) (113)
- Phenotype–genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients (1999) (112)
- An Eph-related receptor protein tyrosine kinase gene segmentally expressed in the developing mouse hindbrain. (1992) (110)
- A screening method to identify genes commonly overexpressed in carcinomas and the identification of a novel complementary DNA sequence. (1995) (110)
- Molecular cloning and chromosomal localization of a human peripheral-type benzodiazepine receptor. (1991) (107)
- Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1: structure, function, regulation of expression and chromosomal localization. (1994) (107)
- Two members of an HNF1 homeoprotein family are expressed in human liver (1991) (105)
- Mapping of the human BAX gene to chromosome 19q13.3-q13.4 and isolation of a novel alternatively spliced transcript, BAX delta. (1995) (105)
- Identification of MAL2, a novel member of the mal proteolipid family, though interactions with TPD52-like proteins in the yeast two-hybrid system. (2001) (104)
- The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuroepithelium and persists in adult pituitary. (1994) (100)
- DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome (2004) (99)
- Genomic organization of collagenous domains and chromosomal assignment of human 180-kDa bullous pemphigoid antigen-2, a novel collagen of stratified squamous epithelium. (1991) (98)
- Structural organization of the porcine and human genes coding for a Leydig cell-specific insulin-like peptide (LEY I-L) and chromosomal localization of the human gene (INSL3). (1994) (96)
- Molecular cloning and expression of cDNAs encoding human alpha-mannosidase II and a previously unrecognized alpha-mannosidase IIx isozyme. (1995) (96)
- Human elastin gene: new evidence for localization to the long arm of chromosome 7. (1991) (94)
- Identification of a new interferon-alpha-inducible gene (p27) on human chromosome 14q32 and its expression in breast carcinoma. (1993) (93)
- Localization of the human Rh blood group gene structure to chromosome region 1p34.3–1p36.1 by in situ hybridization (1991) (93)
- Identification of a new collagen IV chain, alpha 6(IV), by cDNA isolation and assignment of the gene to chromosome Xq22, which is the same locus for COL4A5. (1994) (92)
- Definition of the tumor protein D52 (TPD52) gene family through cloning of D52 homologues in human (hD53) and mouse (mD52). (1996) (92)
- Identification of an immediate early gene, pghs-B, whose protein product has prostaglandin synthase/cyclooxygenase activity. (1992) (91)
- X-Autosome translocations: Cytogenetic characteristics and their consequences (2004) (90)
- Comparative expression of the psoriasin (S100A7) and S100C genes in breast carcinoma and co‐localization to human chromosome 1q21‐q22 (1995) (88)
- Cloning and sequencing of the 52K cathepsin D complementary deoxyribonucleic acid of MCF7 breast cancer cells and mapping on chromosome 11. (1988) (88)
- Cloning and functional expression of a novel degenerin‐like Na+ channel gene in mammals (1999) (88)
- The 30-Kilodalton Protein Present in Purified Fusicoccin Receptor Preparations Is a 14-3-3-Like Protein (1994) (87)
- Structural anomalies of the X chromosome and inactivation center (1981) (87)
- RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene (1999) (86)
- The human 2',5'-oligoadenylate synthetase locus is composed of three distinct genes clustered on chromosome 12q24.2 encoding the 100-, 69-, and 40-kDa forms. (1998) (86)
- The human alpha 2(XI) collagen (COL11A2) chain. Molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization. (1989) (86)
- Chromosomal assignment of retinoic acid receptor (RAR) genes in the human, mouse, and rat genomes. (1991) (85)
- Chromosomal localization of FLT4, a novel receptor-type tyrosine kinase gene. (1992) (83)
- TIF1gamma, a novel member of the transcriptional intermediary factor 1 family. (1999) (81)
- The human hnRNP-M proteins: structure and relation with early heat shock-induced splicing arrest and chromosome mapping (1996) (79)
- Evolutionary study of multigenic families mapping close to the human MHC class I region (1993) (79)
- Human brain factor 1, a new member of the fork head gene family. (1994) (77)
- Structural organization and regulation of the gene for the androgen-dependent glutathione peroxidase-like protein specific to the mouse epididymis. (1993) (77)
- Assignment of vascular endothelial growth factor (VEGF) and placenta growth factor (PLGF) genes to human chromosome 6p12-p21 and 14q24-q31 regions, respectively. (1996) (77)
- The alpha 2(VIII) collagen gene. A novel member of the short chain collagen family located on the human chromosome 1. (1991) (77)
- Neuromuscular defects and breathing disorders in a new mouse model of spinal muscular atrophy (2010) (76)
- Hes1 Is Expressed in the Second Heart Field and Is Required for Outflow Tract Development (2009) (76)
- Cloning and chromosomal location of human alpha 1(XVI) collagen. (1992) (76)
- MG132‐induced progerin clearance is mediated by autophagy activation and splicing regulation (2017) (75)
- Cloning, Chromosomal Localization, and Physical Linkage of the β and γ Subunits (SCNN1B and SCNN1G) of the Human Epithelial Amiloride-Sensitive Sodium Channel (1995) (75)
- The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome (1986) (74)
- TSPY, the Candidate Gonadoblastoma Gene on the Human Y Chromosome, has a Widely Expressed Homologue on the X - Implications for Y Chromosome Evolution (2004) (73)
- Ulip/CRMP proteins are recognized by autoantibodies in paraneoplastic neurological syndromes (1999) (73)
- Gene structure and chromosomal localization of plasma kallikrein. (1991) (73)
- Structure and mapping of the fosB gene. FosB downregulates the activity of the fosB promoter. (1992) (72)
- Bullous pemphigoid antigen (BPAG1): cDNA cloning and mapping of the gene to the short arm of human chromosome 6. (1990) (72)
- Close physical linkage of the FLT1 and FLT3 genes on chromosome 13 in man and chromosome 5 in mouse. (1993) (71)
- Structure, chromosome mapping and expression of the murine Fgf-6 gene. (1990) (71)
- Vanin genes are clustered (human 6q22–24 and mouse 10A2B1) and encode isoforms of pantetheinase ectoenzymes (2001) (71)
- Molecular cloning, functional expression and chromosomal localization of an amiloride‐sensitive Na+ channel from human small intestine (2000) (71)
- Distribution of spontaneous chromosome breaks in man. (1979) (70)
- Localization of new genes and markers to the distal part of the human major histocompatibility complex (MHC) region and comparison with the mouse: new insights into the evolution of mammalian genomes. (1995) (70)
- Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males (2004) (70)
- Cloning of the genes encoding two murine and human cochlear unconventional type I myosins. (1997) (70)
- Human fibulin-1D: molecular cloning, expression and similarity with S1-5 protein, a new member of the fibulin gene family. (1997) (70)
- Molecular cloning of rat human type IX collagen cDNA and localization of the α1(IX) gene on the human chromosome 6 (1989) (70)
- Biochemical and genetic characterization of multiple splice variants of the Flt3 ligand. (1996) (70)
- Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor. (1991) (70)
- Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2). (1999) (68)
- Structural organization and chromosomal localization of the mouse collagenase type I gene. (1995) (68)
- c-Krox Binds to Several Sites in the Promoter of Both Mouse Type I Collagen Genes (1996) (68)
- Stra3/lefty, a retinoic acid-inducible novel member of the transforming growth factor-beta superfamily. (1998) (67)
- Expression of the developmental I antigen by a cloned human cDNA encoding a member of a beta-1,6-N-acetylglucosaminyltransferase gene family. (1993) (66)
- Novel structures CTLA‐2α and CTLA‐2β expressed in mouse activated T cells and mast cells and homologous to cysteine proteinase proregions (1989) (66)
- Chromogranin A. (1995) (65)
- Structure, chromosome mapping and regulation of the mouse zinc-finger gene Krox-24; evidence for a common regulatory pathway for immediate-early serum-response genes. (1989) (65)
- Characterization of the gene for dbpA, a family member of the nucleic-acid-binding proteins containing a cold-shock domain. (1995) (65)
- Cloning of human hepatic nuclear factor 1 (HNF1) and chromosomal localization of its gene in man and mouse. (1990) (64)
- Genomic Organization and Chromosomal Mapping of the Galβ1,3GalNAc/Galβ1,4GlcNAc α2,3-Sialyltransferase (*) (1996) (63)
- Comparative mapping of lipocalin genes in human and mouse: the four genes for complement C8 gamma chain, prostaglandin-D-synthase, oncogene-24p3, and progestagen-associated endometrial protein map to HSA9 and MMU2. (1994) (63)
- Molecular characterization and chromosome localization of a human angiotensin II AT2 receptor gene highly expressed in fetal tissues. (1994) (61)
- Mapping of the galectin-3 gene (LGALS3) to human Chromosome 14 at region 14q21-22 (1997) (61)
- Human CREM gene: evolutionary conservation, chromosomal localization, and inducibility of the transcript. (1993) (60)
- Multiple mRNA isoforms encoding the mouse cardiac Kv1-5 delayed rectifier K+ channel. (1993) (60)
- Tissue‐specific expression of the human laminin α5‐chain, and mapping of the gene to human chromosome 20q13.2‐13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutation (1997) (59)
- Cloning of a parathyroid hormone/parathyroid hormone-related peptide receptor (PTHR) cDNA from a rat osteosarcoma (UMR 106) cell line: chromosomal assignment of the gene in the human, mouse, and rat genomes. (1994) (59)
- Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes (2000) (59)
- ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein (2000) (56)
- Localization of human thyrotropin receptor gene to chromosome region 14q3 by in situ hybridization. (1990) (55)
- Mutation in the 5′ alternatively spliced region of the XNP/ATR-X gene causes Chudley–Lowry syndrome (2005) (53)
- Fim-1, Fim-2/c-fms, and Fim-3, three common integration sites of Friend murine leukemia virus in myeloblastic leukemias, map to mouse chromosomes 13, 18, and 3, respectively (1988) (53)
- Localization of the human c-kit protooncogene on the q11–q12 region of chromosome 4 (1988) (53)
- Cloning of a third member of the D52 gene family indicates alternative coding sequence usage in D52-like transcripts. (1998) (52)
- The gene encoding L1, a neural adhesion molecule of the immunoglobulin family, is located on the X chromosome in mouse and man. (1990) (51)
- Cloning and comparative analysis of the human pre-T-cell receptor alpha-chain gene. (1995) (50)
- Human nidogen: cDNA cloning, cellular expression, and mapping of the gene to chromosome Iq43. (1989) (49)
- Human beta 2 chain of laminin (formerly S chain): cDNA cloning, chromosomal localization, and expression in carcinomas. (1994) (49)
- Trisomy 12p Syndrome: A Chromosomal Disorder Associated with Generalized 3‐Hz Spike and Wave Discharges (1990) (49)
- The FGF-related oncogenes hst and int.2, and the bcl.1 locus are contained within one megabase in band q13 of chromosome 11, while the fgf.5 oncogene maps to 4q21. (1988) (49)
- Definition of a T-Cell Receptor β Gene Core Enhancer of V(D)J Recombination by Transgenic Mapping (2000) (48)
- Trisomy 21 for the region 21q223: Identification by high-resolution R-banding patterns (1981) (48)
- Tumor necrosis factor receptor associated factor 4 (TRAF4) expression pattern during mouse development (1998) (48)
- Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporter (2001) (47)
- Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNA. (1988) (47)
- Constitutional chromosomal breakage (1976) (47)
- Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3. (1987) (47)
- Nucleotide sequence of the gene for human transition protein 1 and its chromosomal localization on chromosome 2. (1990) (47)
- Isolation and chromosomal mapping of a novel ATP-binding cassette transporter conserved in mouse and human. (1997) (47)
- Fibulin-2 (FBLN2): human cDNA sequence, mRNA expression, and mapping of the gene on human and mouse chromosomes. (1994) (47)
- Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases. (1991) (47)
- Two human lysosomal membrane glycoproteins, h-lamp-1 and h-lamp-2, are encoded by genes localized to chromosome 13q34 and chromosome Xq24-25, respectively. (1990) (47)
- Synteny between the loci for a novel FACIT-like collagen locus (D6S228E) and alpha 1 (IX) collagen (COL9A1) on 6q12-q14 in humans. (1992) (46)
- Molecular cloning of a murine N-type calcium channel alpha 1 subunit. Evidence for isoforms, brain distribution, and chromosomal localization. (1994) (46)
- Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15-21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1-11.2, and furin (mouse 7[D1-E2] region). (1991) (45)
- A unique gene encodes spliceoforms of the B-cell adhesion molecule cell surface glycoprotein of epithelial cancer and of the Lutheran blood group glycoprotein (1996) (44)
- Molecular cloning and characterization of the human KIN17 cDNA encoding a component of the UVC response that is conserved among metazoans. (2000) (44)
- The complete primary structure of the human alpha 1 (VIII) chain and assignment of its gene (COL8A1) to chromosome 3. (1991) (43)
- Cloning of Human 2H9 Heterogeneous Nuclear Ribonucleoproteins (1997) (43)
- The highly conserved defender against the death 1 (DAD1) gene maps to human chromosome 14q11–q12 and mouse chromosome 14 and has plant and nematode homologs (1995) (42)
- Centrosome overduplication and mitotic instability in PKD2 transgenic lines (2008) (42)
- A unique gene encodes spliceoforms of the B-cell adhesion molecule cell surface glycoprotein of epithelial cancer and of the Lutheran blood group glycoprotein. (1996) (42)
- Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations (2007) (42)
- Molecular cloning and characterization of mouse LITAF cDNA: role in the regulation of tumor necrosis factor-α (TNF-α) gene expression (2004) (41)
- Cloning and sequence of a secretory protein induced by growth factors in mouse fibroblasts. (1989) (41)
- The Gene Encoding Human Splicing Factor 9G8 (1995) (41)
- The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region (1997) (40)
- Cloning and sequencing of the mouse Gli2 gene: localization to the Dominant hemimelia critical region. (1997) (40)
- A Human-Mouse Chimera of the α3α4α5(IV) Collagen Protomer Rescues the Renal Phenotype in Col4a3−/− Alport Mice (2003) (40)
- A transformed human tracheal gland cell line, MM-39, that retains serous secretory functions. (1996) (39)
- The genes for human brain factor 1 and 2, members of the fork head gene family, are clustered on chromosome 14q. (1995) (39)
- The human H-twist gene is located at 7p21 and encodes a B-HLH protein that is 96% similar to its murine M-twist counterpart (1996) (39)
- Subcellular distribution of HP1 proteins is altered in ICF syndrome (2005) (38)
- The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23. (1993) (38)
- The human amiloride-sensitive Na+/H+ antiporter: localization to chromosome 1 by in situ hybridization. (1988) (37)
- The KUP gene, located on human chromosome 14, encodes a protein with two distant zinc fingers. (1991) (37)
- Cloning and characterization of the mouse homologue of the human dendritic cell maturation marker CD208/DC‐LAMP (2003) (37)
- Molecular basis and expression of the LWa/LWb blood group polymorphism. (1995) (37)
- Extensive analysis of duplicated-inverted hepatitis B virus integrations in human hepatocellular carcinoma. (1998) (37)
- Mapping of the human retinoic acid receptor to the q21 band of chromosome 17 (1988) (37)
- Lhx9 and Lhx9α LIM-homeodomain factors: genomic structure, expression patterns, chromosomal localization, and phylogenetic analysis. (2000) (36)
- Localization of a novel ryanodine receptor gene (RYR3) to human chromosome 15q14-q15 by in situ hybridization. (1993) (36)
- Poly(ADP-ribose) polymerase interacts with a novel human ubiquitin conjugating enzyme: hUbc9. (1997) (36)
- Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach (2004) (36)
- Molecular cloning of a mammalian ABC transporter homologous to Drosophila white gene (1996) (36)
- Human laminin A chain (LAMA) gene: chromosomal mapping to locus 18p11.3. (1989) (35)
- Two human genes related to murine vanin-1 are located on the long arm of human chromosome 6. (1998) (35)
- Structure, sequence, and chromosomal location of the gene for USF2 transcription factors in mouse. (1995) (35)
- cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I. (1997) (34)
- Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridization. (1993) (34)
- A new Groucho TLE4 protein may regulate the repressive activity of Pax5 in human B lymphocytes (2002) (34)
- Chromosomal localization of the delta opioid receptor gene to human 1p34.3-p36.1 and mouse 4D bands by in situ hybridization. (1994) (34)
- Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin gene (1990) (34)
- Chromosomal mapping of two novel human FGF genes, FGF11 and FGF12. (1997) (33)
- Cloning, chromosomal localization, and physical linkage of the beta and gamma subunits (SCNN1B and SCNN1G) of the human epithelial amiloride-sensitive sodium channel. (1995) (33)
- Characterization of the human jumonji gene. (1996) (33)
- The genes for nicein/kalinin 125- and 100-kDa subunits, candidates for junctional epidermolysis bullosa, map to chromosomes 1q32 and 1q25-q31. (1994) (33)
- Localization of the mcf.2 transforming sequence to the X chromosome. (1987) (32)
- The structural gene for aldolase B (ALDB) maps to 9q13→32 (1985) (32)
- Laser microdissection of the fragile X region: identification of cosmid clones and of conserved sequences in this region. (1991) (32)
- POLYMORPHIC DNA MARKERS IN PRENATAL DIAGNOSIS OF FRAGILE X SYNDROME (1985) (32)
- Structural organization, chromosomal localization, expression and phylogenetic evaluation of mouse glutathione peroxidase encoding genes. (1996) (32)
- In human pachytene spermatocytes, SUMO protein is restricted to the constitutive heterochromatin (2008) (32)
- Genes of the membrane-type matrix metalloproteinase (MT-MMP) gene family, MMP14, MMP15, and MMP16, localize to human chromosomes 14, 16, and 8, respectively. (1997) (31)
- Isolation and sequencing of cDNAs and genomic DNAs encoding the alpha 4 chain of basement membrane collagen type IV and assignment of the gene to the distal long arm of human chromosome 2. (1992) (31)
- Characterization and chromosomal assignment of a human cDNA encoding a protein related to the murine 102-kDa cadherin-associated protein (alpha-catenin). (1993) (31)
- Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11-->q12 and mouse chromosome 14D1-E1 by in situ hybridization. (1996) (31)
- Structure of the mouse dipeptidyl peptidase IV (CD26) gene. (1994) (30)
- Chromosomal localization of the three members of the jun proto-oncogene family in mouse and man. (1990) (30)
- hH-Rev107, a class II tumor suppressor gene, is expressed by post-meiotic testicular germ cells and CIS cells but not by human testicular germ cell tumors (2001) (30)
- The human calbindin D28k (CALB1) and calretinin (CALB2) genes are located at 8q21.3----q22.1 and 16q22----q23, respectively, suggesting a common duplication with the carbonic anhydrase isozyme loci. (1991) (30)
- Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis (2004) (30)
- Cloning of human striatin cDNA (STRN), gene mapping to 2p22-p21, and preferential expression in brain. (1998) (30)
- Cloning of human α1(X) collagen DNA and localization of the COL10A1 gene to the q21–q22 region of human chromosome 6 (1991) (29)
- Cloning, expression, and chromosomal mapping of a human ATPase II gene, member of the third subfamily of P-type ATPases and orthologous to the presumed bovine and murine aminophospholipid translocase. (1999) (29)
- The human 2',5'-oligoadenylate synthetase-like gene (OASL) encoding the interferon-induced 56-kDa protein maps to chromosome 12q24.2 in the proximity of the 2',5'-OAS locus. (1999) (29)
- Assignment of the human stromelysin 3 (STMY3) gene to the q11.2 region of chromosome 22. (1992) (29)
- Cloning of the mouse gene encoding plasma glutathione peroxidase: organization, sequence and chromosomal localization. (1995) (29)
- Further evidence for the dispersion of the human fibrillar collagen genes. (1986) (28)
- The gene encoding the human spasmolytic protein (SML1/hSP) is in 21q 22.3, physically linked to the homologous breast cancer marker gene BCEI/pS2. (1992) (28)
- Molecular cloning of human RP105 (1997) (28)
- Genomic organization of the human SPOCK gene and its chromosomal localization to 5q31. (1998) (28)
- Maternal age and origin of non-disjunction in trisomy 21. (1980) (27)
- Cloning and mapping of murine Nfe2l1. (1995) (27)
- Mechanism of intrachromosomal triplications 15q11‐q13: A new clinical report (2003) (27)
- The murine M-CSF gene is localized on chromosome 3. (1989) (27)
- Structure and Expression of the ATFa Gene* (1996) (27)
- Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation (2001) (26)
- Bivalent 15 Regularly Associates With the Sex Vesicle in Normal Male Meiosis (2004) (26)
- Assignment of the human hap retinoic acid receptor RAR beta gene to the p24 band of chromosome 3. (1988) (26)
- A t(3;8) chromosomal translocation associated with hepatitis B virus intergration involves the carboxypeptidase N locus (1996) (26)
- Assignment of the human interferon-alpha receptor gene to chromosome 21q22.1 by in situ hybridization. (1990) (25)
- Identification of a precursor genomic segment that provided a sequence unique to glycophorin B and E genes. (1993) (25)
- A human-mouse chimera of the alpha3alpha4alpha5(IV) collagen protomer rescues the renal phenotype in Col4a3-/- Alport mice. (2003) (25)
- Homologous chromosomal locations of the four genes for inter-α-inhibitor and pre-α-inhibitor family in human and mouse: Assignment of the ancestral gene for the lipocalin superfamily (1992) (25)
- Localization of the thyroglobulin gene by in situ hybridization to human chromosomes (2004) (25)
- The human FGF9 gene maps to chromosomal region 13q11-q12. (1995) (24)
- Assignment of a new congenital fibrosis of extraocular muscles type 3 (CFEOM3) locus, FEOM4, based on a balanced translocation t(2;13) (q37.3;q12.11) and identification of candidate genes (2005) (24)
- Assignment of the humanhap retinoic acid receptor RARβ gene to the p24 band of chromosome 3 (1988) (24)
- Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects (1976) (24)
- Human testis specifically expresses a homologue of the rodent T lymphocytes RT6 mRNA (1996) (23)
- The high-affinity interleukin 8 receptor gene (IL8RA) maps to the 2q33-q36 region of the human genome: cloning of a pseudogene (IL8RBP) for the low-affinity receptor. (1993) (23)
- The human intercellular adhesion molecule 3 (ICAM3) gene is located in the 19p13.2-p13.3 region, close to the ICAM1 gene. (1994) (23)
- A human interstitial telomere associates in vivo with specific TRF2 and TIN2 proteins (2002) (23)
- HP1β and HP1γ, but not HP1α, decorate the entire XY body during human male meiosis (2004) (23)
- Lhx9 and Lhx9alpha LIM-homeodomain factors: genomic structure, expression patterns, chromosomal localization, and phylogenetic analysis. (2000) (23)
- Novel structures CTLA-2 alpha and CTLA-2 beta expressed in mouse activated T cells and mast cells and homologous to cysteine proteinase proregions. (1989) (23)
- Chromosomal location of two human genes encoding tetrahydrobiopterin-metabolizing enzymes: 6-pyruvoyl-tetrahydropterin synthase maps to 11q22.3-q23.3, and pterin-4 alpha-carbinolamine dehydratase maps to 10q22. (1994) (23)
- Fertile Homozygous Transgenic Mice Expressing a Functional Truncated Herpes Simplex Thymidine Kinase ΔTK Gene (1998) (22)
- Monosomy 21: a new case confirmed by in situ hybridization (1987) (22)
- Four new cases of dicentric Y chromosomes (1977) (22)
- Locations of the ets subfamily members net, elk1, and sap1 (ELK3, ELK1, and ELK4) on three homologous regions of the mouse and human genomes. (1995) (22)
- Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1 (1986) (22)
- Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication‐deletion of chromosome 9 and gene dosage effect for adenylate kinase‐1 (1980) (22)
- Molecular analysis of a hybrid gene encoding human glycophorin variant Miltenberger V-like molecule. (1990) (21)
- In situ hybridization localizes the human OTF3 to chromosome 6p21.3-->p22 and OTF3L to 12p13. (1993) (21)
- Linkage studies of X-linked mental retardation: High frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome) (2004) (21)
- Identification of a human 17p-located cDNA encoding a protein of the Snf2-like helicase family. (1998) (20)
- Genomic organization and chromosomal localization of the murine epididymal retinoic acid‐binding protein (mE‐RABP) gene (1998) (20)
- Identification of human and mouse HIRA-interacting protein-5 (HIRIP5), two mammalian representatives in a family of phylogenetically conserved proteins with a role in the biogenesis of Fe/S proteins. (2001) (20)
- VPREB3: cDNA characterization and expression in human and chromosome mapping in human and mouse (2000) (20)
- A dynamic study in two new cases of X chromosome translocations (1978) (20)
- [Partial trisomy 13 due to maternal translocation t(2;13)]. (1977) (20)
- The human basic fibroblast growth factor gene is located on the long arm of chromosome 4 at bands q26-q27. (1990) (20)
- Molecular cloning and characterization of mouse LITAF cDNA: role in the regulation of tumor necrosis factor-alpha (TNF-alpha) gene expression. (2004) (20)
- Organization of the X and Y chromosomes in human, chimpanzee and mouse pachytene nuclei using molecular cytogenetics and three-dimensional confocal analyses (2000) (19)
- Molecular cloning, chromosomal localization, and expression analysis of CYRN1 and CYRN2, two human genes coding for cyritestin, a sperm protein involved in gamete interaction. (1998) (19)
- Characterization of Two Age-induced Intracisternal A-particle-related Transcripts in the Mouse Liver (1997) (19)
- One subunit of the transcription factor NF-Y maps close to the major histocompatibility complex in murine and human chromosomes. (1991) (18)
- The Sycp1 loci of the mouse genome: successive retropositions of a meiotic gene during the recent evolution of the genus. (1997) (18)
- Chromosomal localization and expression pattern of the RNase L inhibitor gene (1996) (18)
- Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association. (1992) (18)
- X-linked mental retardation with the fragile X. A study of 15 families (2004) (18)
- Genomic analysis of the 67-kDa laminin receptor in normal and pathological tissues: circumstantial evidence for retroposon features. (1991) (18)
- Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18 (1999) (18)
- [Trisomy 8 in mosaicism]. (1975) (18)
- A human RNA polymerase II subunit is encoded by a recently generated multigene family (2001) (18)
- Chromosomal localisation of the mouse and human peripherin genes. (1992) (18)
- Assignment of the gene for neuroendocrine protein 7B2 (SGNE1 locus) to mouse chromosome region 2[E3-F3] and to human chromosome region 15q11-q15. (1990) (18)
- Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study. (1998) (18)
- Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7 * (1985) (18)
- Activation of a mcf.2 oncogene by deletion of amino-terminal coding sequences. (1988) (17)
- Human GTP-cyclohydrolase I gene and sepiapterin reductase gene map to region 14q21-q22 and 2p14-p12, respectively, by in situ hybridization. (1995) (17)
- YAC-assisted cloning of a putative G-protein mapping to the MHC class I region. (1992) (17)
- HP1beta and HP1gamma, but not HP1alpha, decorate the entire XY body during human male meiosis. (2003) (17)
- Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B (2004) (17)
- Prader-Willi syndrome and chromosome 15 (1983) (17)
- Sialoadhesin (Sn) maps to mouse chromosome 2 and human chromosome 20 and is not linked to the other members of the sialoadhesin family, CD22, MAG, and CD33. (1995) (17)
- Assignment of human G-protein-coupled inward rectifier K+ channel homolog GIRK3 gene to chromosome 1q21-q23. (1995) (17)
- Assignment of the human weak inward rectifier K+ channel TWIK-1 gene to chromosome 1q42-q43. (1996) (17)
- Chromosomal localization of the mouse gene coding for vimentin. (1989) (16)
- Assignment of the human tear lipocalin gene (LCN1) to 9q34 by in situ hybridization. (1993) (16)
- Localization of the HST/FGFK gene with regard to 11 q 13 chromosomal breakpoint and fragile site (1991) (16)
- The human pre-B-specific λ-like cluster is located in the 22q11.2–22q12.3 region, distal to the IgCλ locus (1991) (16)
- Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation (1979) (16)
- Isolation and regional mapping of cDNAs expressed during early human development. (1997) (16)
- The murine polycomb-group genes Ezh1 and Ezh2 map close to Hox gene clusters on mouse Chromosomes 11 and 6 (1999) (16)
- Localization of the gene encoding peptidylglycine alpha-amidating monooxygenase (PAM) to human chromosome 5q14-5q21. (1993) (16)
- The murine erythropoietin gene is localized on chromosome 5. (1988) (16)
- Assignment of the human membrane-type matrix metalloproteinase (MMP14) gene to 14q11-q12 by in situ hybridization. (1995) (16)
- Assignment of the human gamma-glutamyl transferase gene to the long arm of chromosome 22 (1987) (15)
- Molecular cloning of rat and human type IX collagen cDNA and localization of the alpha 1(IX) gene on the human chromosome 6. (1989) (15)
- Identification and in situ hybridization mapping of a mouse Tpd52l1 (D53) orthologue to chromosome 10A4–B2 (1998) (15)
- Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site (2004) (15)
- Dicentric Robertsonian translocation in man. 17 cases studied by R,C, and N banding. (1979) (15)
- Localization of the human T-cell receptor gamma locus (TCRG) to 7p14----p15 by in situ hybridization. (1991) (15)
- Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome (1993) (15)
- A third human CBL gene is on chromosome 19. (1998) (15)
- Composition and chromosomal localization of the small multigene family encoding mouse U3B nucleolar RNA. (1991) (14)
- Chromosomal Localization of the Adrenoleukodystrophy-Related Gene in Man and Mice (1997) (14)
- Dicentric Robertsonian translocations in man (2004) (14)
- Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome. (1978) (14)
- The OLFR1 gene encoding the HGMP07E putative olfactory receptor maps to the 17p13-->p12 region of the human genome and reveals an MspI restriction fragment length polymorphism. (1993) (14)
- Chromosomal localization of murine ryanodine receptor genes RYR1, RYR2, and RYR3 by in situ hybridization. (1994) (14)
- Genomic organization and chromosomal mapping of the Gal beta 1,3GalNAc/Gal beta 1,4GlcNAc alpha 2,3-sialyltransferase. (1996) (13)
- Molecular cloning, cDNA analysis, and localization of a monomer of the N-acetylglucosamine-specific receptor of the thyroid, NAGR1, to chromosome 19p13.3-13.2. (1994) (13)
- Erythrocyte copper levels in children with trisomy 21. (2008) (13)
- cDNA cloning, expression and chromosomal localization of the murine AF-4 gene involved in human leukemia (1998) (13)
- Assignment of the mouse desmin gene to chromosome 1 band C3. (1990) (13)
- Different chromosomal localization of two adenylyl cyclase genes expressed in human brain (1992) (13)
- Chromosomal location of the Syk and ZAP-70 tyrosine kinase genes in mice and humans (2004) (13)
- Clinical and molecular study of DiGeorge sequence (1994) (13)
- Colocalization of the genes coding for the α3 and β3 subunits of soluble guanylyl cyclase to human chromosome 4 at q31.3–q33 (1993) (13)
- Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents (1979) (13)
- Presence of a TaqI polymorphism in the human glutamate dehydrogenase (GLUD) gene on chromosome 10. (1987) (12)
- Chromosomal localization of two genes encoding human ras exchange factors: SOS1 maps to the 2p22-->p16 region and SOS2 to the 14q21-->q22 region of the human genome. (1994) (12)
- Assignment of the human progesterone receptor to the q22 band of chromosome 11 (2004) (12)
- Quantitative and qualitative study of acrocentric associations in 109 normal subjects (1976) (12)
- Genomic structure and chromosomal location of the mouse pre-T-cell receptor alpha gene (2004) (12)
- Genomic structure and developmental expression of the mouse cell cycle regulatory transcription factor DP1. (1996) (12)
- Biochemical and Genetic Characterization of Multiple Splice Variants of the Flt 3 Ligand (2002) (11)
- A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter→p22::p22→qter)) (1977) (11)
- Assignment of the human lipoprotein lipase (LPL) gene to chromosome band 8p22. (1993) (11)
- Chromosomal localization of three human poly(A)-binding protein genes and four related pseudogenes (1999) (11)
- Origin of the extra chromosome in trisomy 21 (1979) (11)
- Chromosomal localization of human homologs of the Drosophila heterochromatin protein 1 (HP1) gene (2004) (11)
- Synteny comparison between apes and human using fine-mapping of the genome. (2002) (11)
- Immunoreactive SOD‐1 in Amniotic Fluid, Amniotic Cells and Fibroblasts from Trisomy 21 Fetus (1985) (11)
- Assignment of transcription factor NFAT5 to human chromosome 16q22.1, murine chromosome 8D and porcine chromosome 6p1.4 and comparison of the polyglutamine domains (2000) (11)
- Assignment of tumor protein p53 induced nuclear protein 1 (TP53INP1) gene to human chromosome band 8q22 by in situ hybridization (2002) (11)
- Heterochromatin, from Chromosome to Protein (2011) (11)
- The gene (POLR2L) encoding the hRPB7.6 subunit of human RNA polymerase. (1996) (10)
- The mouse and human IGSF6 (DORA) genes map to the inflammatory bowel disease 1 locus and are embedded in an intron of a gene of unknown function (2000) (10)
- In situ hybridization and pulsed-field gel analysis define two major minisatellite loci: 1q23 for minisatellite 33.6 and 7q35-q36 for minisatellite 33.15. (1989) (10)
- Assignment of ISG20 encoding a new interferon-induced PML nuclear body-associated protein, to chromosome 15q26 by in situ hybridization. (1997) (10)
- Proximity of the CTLA-1 serine esterase and Tcrα loci in mouse and man (2004) (10)
- The mouseCD3-γ, -δ, and -ε genes reside within 50 kilobases on chromosome 9, whereasCD3-ζ maps to chromosome 1, band H (2004) (10)
- Structure and putative function of a murine epididymal retinoic acid-binding protein (mE-RABP). (1998) (10)
- Neurological disorder in transgenic mice that express the large T antigen of polyoma virus in the nervous system. (1989) (10)
- Assignment of the Human Amiloride-Sensitive Na+Channel δ Isoform to Chromosome 1p36.3–p36.2 (1996) (10)
- Forthcoming Papers (1991) (10)
- Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p (1980) (9)
- Genomic structure and chromosomal localization of the mouse CDEI-binding protein CDEBP (APLP2) gene and promoter sequences. (1996) (9)
- Assignment of the tumor protein p53 induced nuclear protein 2 (TP53INP2) gene to human chromosome band 20q11.2 by in situ hybridization (2004) (9)
- The human paired domain gene PAX7 (Hup1) maps to chromosome 1p35-1p36.2. (1993) (9)
- Evolutionary conservation and chromosomal localization of flvi-1. (1991) (9)
- Mouse ferritin H sequences map to chromosomes 3, 6, and 19. (1991) (9)
- Special Notice to Contributors and Subscribers (1976) (9)
- Genomic organization and the tissue distribution of alternatively spliced isoforms of the mouse Spatial gene (2004) (9)
- Colocalization of the genes coding for the alpha 3 and beta 3 subunits of soluble guanylyl cyclase to human chromosome 4 at q31.3-q33. (1993) (9)
- Chromosomal localization of two mouse genes encoding thymus-specific serine peptidase and thymus-expressed acidic protein (2000) (9)
- Proximity of the CTLA-1 serine esterase and Tcr alpha loci in mouse and man. (1988) (9)
- The fibulin-1 gene (FBLN1) is located on human chromosome 22 and on mouse chromosome 15. (1994) (9)
- Integration of H-2Z1, a Somatosensory Cortex-Expressed Transgene, Interferes with the Expression of the Satb1 and Tbc1d5 Flanking Genes and Affects the Differentiation of a Subset of Cortical Interneurons (2012) (9)
- Assignment of FGF13 to human chromosome band Xq21 by in situ hybridization. (1997) (8)
- Chromosomal mapping of human adenylyl cyclase genes type III, type V and type VI (1994) (8)
- Assignment of mouse nicein genes to Chromosomes 1 and 18 (1994) (8)
- Assignment by in situ hybridization of a fibroblast growth factor receptor gene to human chromosome band 10q26 (2005) (8)
- Partial inversion of the secondary constriction of chromosome 9. Does it exist? (2004) (8)
- The myosin light chain kinase gene is not duplicated in mouse: partial structure and chromosomal localization of Mylk. (2001) (8)
- The mouse CD3-gamma, -delta, and -epsilon genes reside within 50 kilobases on chromosome 9, whereas CD3-zeta maps to chromosome 1, band H. (1989) (8)
- Chromosomal localization of mouse and human neurotensin receptor genes (1994) (8)
- Fine mapping of the long arm of human chromosome 11 by in situ hybridization using different translocations, including the t(11;22) of Ewing sarcoma. (1990) (8)
- Physical mapping of an Xq-proximal interstitial duplication in a male (1992) (8)
- Chimpanzee Rh-like blood group genes map to chromosome region 1p36.1-->p34.2 by in situ hybridization. (1994) (8)
- Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site. (1988) (8)
- Assignment of secretogranin I locus to mouse chromosome 2 by in situ hybridization and interspecific backcross analysis. (1991) (8)
- Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies. (1997) (8)
- PHTF, a novel atypical homeobox gene on chromosome 1p13, is evolutionarily conserved. (1999) (7)
- [The evolution of epilepsy in the most common genetic forms with mental retardation (Down's syndrome and the fragile X syndrome)]. (1993) (7)
- Maternally inherited duplication of the possible imprinted 14q31 region (2001) (7)
- An Eph-related receptor protein tyrosine kinase gene segmentally expressed in the developing mouse hindbrain. (1992) (7)
- Organization and chromosomal localization of the gene (TAF2H) encoding the human TBP-associated factor II 30 (TAFII30). (1995) (7)
- Assignment of tumor protein p53 induced nuclear protein 1 (TP53INP1) gene to human chromosome band 8q22 by in situ hybridization. (2002) (7)
- Localization of the human phosphotyrosine phosphatase-related genes (h-PRL-1) to chromosome bands 1p35–p34, 17q12–q21, 11q24–q25 and 12q24 (1996) (7)
- Localization of the mouse Mcf-2 (Dbl) protooncogene within a conserved linkage group on the mouse X chromosome. (1990) (6)
- Mapping of the Tuple1 gene to mouse chromosome 16A-B1. (1994) (6)
- Localization of the genes for human inositol 1,4,5-trisphosphate 3-kinase A (ITPKA) and B (ITPKB) to chromosome regions 15q14-q21 and 1q41-q43, respectively, by in situ hybridization. (1992) (6)
- cDNA cloning and localization of the mouse leukosialin gene (Ly48) to chromosome 7 (2005) (6)
- Mapping of the dopa decarboxylase gene to the 11A band of the murine genome. (1992) (6)
- Isolation of 37 single-copy DNA probes from human chromosome 6 and physical mapping of 11 probes by in situ hybridization. (1991) (6)
- Assignment1 of Stra13 to the sub-telomeric region of mouse chromosome 6 by in situ hybridization (2000) (6)
- The gene encoding the large human neurofilament subunit (NF-H) maps to the q121–q131 region on human chromosome 22 (1988) (6)
- Study of a family with a fragile site of the X chromosome at Xq27–28 without mental retardation (1989) (6)
- Chromosomal localizations of mouse Fgf2 and Fgf5 genes (2004) (6)
- The Gene and Pseudogenes of Cbx3/mHPlγ (2001) (6)
- Famillial pericentric inversion of chromosome 9, INV (9)(p22q32) with recurrent duplication‐deletion (1983) (6)
- [Acrocentric associations in parents of mongol children]. (1974) (6)
- Isolation and chromosomal location of mE4, a novel murine gene of the immunoglobulin superfamily (1996) (6)
- A novel C2H2 zinc-finger protein gene (ZNF160) maps to human chromosome 19q13.3-q13.4. (1995) (6)
- Juxtaposition of N‐myc and Igk through a reciprocal t(6;12) translocation in a mouse plasmacytoma (1994) (5)
- Physical and genetic localization of the gamma subunit of the cyclic GMP phosphodiesterase on the long arm of chromosome 17 (17q25). (1993) (5)
- Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein (1997) (5)
- Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21 (1986) (5)
- EXPRESSION ANORMALE DE SEQUENCES DU VIRUS DE L'HEPATITE B INTEGREES DANS DES CARCINOMES HEPATOCELLULAIRES HUMAINS (1992) (5)
- Localization of the gene for amiloride binding protein on chromosome 7 and RFLP analysis in cystic fibrosis families (1990) (5)
- Localization of human transcription factor TEF-4 and TEF-5 (TEAD2, TEAD3) genes to chromosomes 19q13.3 and 6p21.2 using fluorescence in situ hybridization and radiation hybrid analysis. (1999) (5)
- Cloning and chromosome localization of the mouse Ews gene. (1994) (5)
- Assignment of LCN1 to human chromosome 9 is confirmed. (1995) (5)
- Mouse α1 type V collagen gene maps to the [A2-B] region of chromosome 2 (1993) (4)
- Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12. (1977) (4)
- Chromosome Studies in 1942 Women before Artificial Insemination with Donor Semen (1980) (4)
- Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation (2005) (4)
- Advantages of silver staining in seven rearrangements of acrocentric chromosomes, excluding robertsonian translocations (2004) (4)
- Le syndrome d'Angelman (1994) (4)
- Erratum to the report of the third international workshop on human Y chromosome mapping 1997 (1997) (4)
- Erratum to the report of the third international workshop on human Y chromosome mapping 1997 (1997) (4)
- Assignment of IL12RB2 to human chromosome 1p31.3-->p31.2 between D1S230 and D1S198. (1997) (4)
- In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3. (1991) (4)
- Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridization (1989) (4)
- Chromosome localization and polymorphism of an oestrogen-inducible gene specifically expressed in some breast cancers (1988) (4)
- Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization (1988) (4)
- Three new cases of partial monosomy 21 resulting from one ring 21 chromosome and two unbalanced reciprocal translocations (1984) (4)
- Homologous chromosomal locations of the four genes for inter-alpha-inhibitor and pre-alpha-inhibitor family in human and mouse: assignment of the ancestral gene for the lipocalin superfamily. (1992) (4)
- Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation (1988) (4)
- In humans all U3 genes map to chromosome 17p12-->p11, but in mouse the U3A and U3B genes are located on different chromosomes. (1993) (4)
- Localization of the Rab escort protein-2 (REP2) and inositol 1,4,5-trisphosphate 3-kinase (ITPKB) genes to mouse chromosome 1 by in situ hybridization and precision of the syntenic regions between mouse and human 1q42-q44. (1997) (4)
- Assignment of the human amiloride-sensitive Na+ channel delta isoform to chromosome 1p36.3-p36.2. (1996) (4)
- Comparative Assignments of the Genes of the Inter-α-inhibitor Family in Human and Mouse:ITIH4Is Close toITIH1andITIH3,on HSA 3 and MMU 14 (1997) (4)
- Assignment of Fgf12 to mouse chromosome bands 16B1-->B3 by in situ hybridization. (1997) (3)
- Localization of human calcyphosine gene (CAPS) to the p13.3 region of chromosome 19 by in situ hybridization. (1990) (3)
- Mapping of the human 60 000 MrRo/SSA locus: the genes for three Ro/SSA autoantigens are located on separate chromosomes (2004) (3)
- Tg (9 HSA-MYC), a homozygous lethal insertion in the mouse (2004) (3)
- The B-HLH protein encoding the M-twist gene is located by in situ hybridization on murine Chromosome 12 (2004) (3)
- [The chromosome 13 in ring syndrome]. (1975) (3)
- [Small supernumerary chromosomes]. (1985) (3)
- Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin gene. (1992) (3)
- cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31 (1988) (3)
- Screening for subtelomeric rearrangements using automated fluorescent genotyping of microsatellite markers: a Lebanese study. (2006) (3)
- Immunoreactive Copper‐Zinc Superoxide‐dismutase (SOD‐1) in Mosaic Trisomy 21 and Normal Subjects (1984) (3)
- Brief Gene Mapping Reports A / B / C / D / E / F / G (2002) (3)
- Syndrome de Smith-Magenis (1997) (2)
- Cloning and mapping of murine Idd: conserved synteny of the DiGeorge syndrome critical region (1997) (2)
- Localization of the gene (TAF2D) encoding the 100-kDa subunit (hTAFII100) of the human TFIID complex to chromosome 10 band q24-q25.2. (1996) (2)
- Localization of mouse parathyroid hormone-like peptide gene (Pthlh) to distal chromosome 6 using interspecific backcross mice and in situ hybridization. (1992) (2)
- Assignment of HBRM, the human homolog of S. cerevisiae SNF2/SWI2 and Drosophila brm genes, to chromosome region 9p23–p24, by in situ hybridization (1994) (2)
- Mapping of the MR60/ERGIC-53 gene to human Chromosome 18q21.3–18q22 by in situ hybridization (1996) (2)
- [Interstitial deletion of chromosome 7 (7q33 to q35)]. (1982) (2)
- Clinical and Genetic Heterogeneity of Leber’s Congenital Amaurosis (1993) (2)
- Physical mapping of the 17p chromosomal region relationship with the charcot marie tooth disease (1991) (2)
- Abnormal Childhood Phenotypes Associated with the Same “Balanced” Chromosome Rearrangements as In the Parents (2008) (2)
- [Balanced chromosome rearrangements with abnormal phenotype]. (1988) (2)
- Chromosomal localization of human RNA polymerase II subunit genes. (1994) (2)
- In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13 (2004) (2)
- Calendar of Events 1992 (1992) (2)
- Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;q11) (1984) (2)
- The human pre-B-specific lambda-like cluster is located in the 22q11.2-22q12.3 region, distal to the IgC lambda locus. (1991) (2)
- Molecular Cloning of an Inducible Cytotoxic T-Lymphocyte-Associated Gene (Hu-CTLA 1) and Gene Localization to Human Chromosome 14 (1989) (2)
- Inherited haemolytic anaemia created by insertional inactivation of the α-spectrin gene (1992) (2)
- [Smith-Magenis syndrome]. (1997) (2)
- A panel of deleted mouse X chromosome somatic cell hybrids derived from the embryonic stem cell line HD3 shows preferential breakage in the Hprt-DXHX254E region. (1993) (2)
- Molecular cloning and characterization of a mono(ADP-ribosyl)transferase from human testis. (1997) (1)
- [Partial trisomy 13 due to t(X;13) translocation. Contribution of in situ hybridization]. (1987) (1)
- [Pericentric inversions: studies in 47 cases]. (1979) (1)
- [Partial trisomy 11q and familial translocation 11--22 (author's transl)]. (1975) (1)
- Chromosomal localization of human aspartate aminotransferase genes by in situ hybridization (1989) (1)
- [Trisomy 4p. Three new observations (author's transl)]. (1975) (1)
- A new human hypervariable locus (K29) maps to the q37.3 region of chromosome 2 and reveals a fingerprint. (1991) (1)
- [Partial trisomy 21]. (1979) (1)
- [Long Y chromosome (Yq+) and phenotype abnormalities. Fluorescence study]. (1973) (1)
- 105 The 11q13 region in human tumors (1989) (1)
- Molecular cloning of a murine N‐type calcium channel α1 subunit (1)
- Chromosomal localization of the human and mouse histidine decarboxylase genes by in situ hybridization. Exclusion of the HDC gene from the Prader-Willi syndrome region (1996) (1)
- [Partial deletion of the short arm of an X chromosome]. (1974) (1)
- pmcf.2-11, a single copy clone from chromosomal region 12q12-q13.1 [D12S32]. (1988) (1)
- A DP1 pseudogene derived from an aberrantly processed RNA. (1997) (1)
- Mouse Fgf9 (fibroblast growth factor 9) is localized on chromosome 14 (1997) (1)
- [Abnormal expression of hepatitis B virus sequences integrated in human hepatocellular carcinomas]. (1992) (1)
- Comparative assignments of the genes of the inter-alpha-inhibitor family in human and mouse: ITIH4 is close to ITIH1 and ITIH3, on HSA 3 and MMU 14. (1997) (1)
- Sublocalization of the mouse parathyroid hormone-like peptide gene to distal chromosome 6 by interspecific backcross analysis and in situ hybridization (1992) (0)
- [Contribution of in situ hybridization to chromosomal analysis]. (1985) (0)
- Contents, Vol. 79, 1997 (1997) (0)
- Werner Schmid, 1930–2002 (2002) (0)
- Revised guidelines for authors of gene mapping reports (2000) (0)
- HumanElastin Gene:New Evidence forLocalization totheLong Arm ofChromosome7 (1991) (0)
- [Disorders of gastric secretion in malnutrition states]. (1969) (0)
- Subject Index, Vol. 76, 1997 (1997) (0)
- Subject Index Vol. 65, 1994 (1994) (0)
- The large neurofilament subunit nf h of the rat complementary dna cloning in situ detection and localization of the human nf h gene (1989) (0)
- Mouse orphan nuclear receptor Rev-erb beta sequences are localized on chromosomes 19 and 14. (1996) (0)
- [Angelman syndrome]. (1994) (0)
- Crytic translocation resulting in Angelman syndrome Implication for genetic counselling (2002) (0)
- Mouse Fgf7 (fibroblast growth factor 7) and Fgf8 (fibroblast growth factor 8) genes map to Chromosomes 2 and 19 respectively (1995) (0)
- Eleventh International Chromosome Conference (2004) (0)
- Contents, Vol. 63, 1993 (1993) (0)
- Clinical and molecular basis of the X‐linked α‐thalassemia and mental retardation syndrome (ATR‐X) (2003) (0)
- Expression cloning of a murine delta opioid receptor (1994) (0)
- [Maternal age in trisomy 21]. (1979) (0)
- Subject Index Vol. 89, 2000 (2000) (0)
- Contents Vol. 87, 1999 (2000) (0)
- [Mental retardation linked to fragility of chromosome X: current knowledge]. (1984) (0)
- Participation of host cells: resistance or collaboration (2004) (0)
- Mouse orphan nuclear receptor Rev-erbβ sequences are localized on Chromosomes 19 and 14 (1996) (0)
- Molecular cloning and expression of cDNAs encoding human a-mannosidase II and a previously unrecognized a-mannosidase lix isozyme (2005) (0)
- [Refractory sideroblastic anemia, three cases with the same extra marker chromosome (47, Mar +) (author's transl)]. (1977) (0)
- Rev 107 , a class II tumor suppressor gene , is expressed by post-meiotic testicular germ cells and CIS cells but not by human testicular germ cell tumors (2019) (0)
- The mouse plasma glutathione peroxidase‐encoding gene: Organization, tissue‐distribution and chromosomal localization (1995) (0)
- Subject Index Vol. 60, 1992 (1992) (0)
- Position-dependent variegation of a CD4 minigene specifically expressed in mature CD4+ T cells (1997) (0)
- Contents Vol. 89, 2000 (2000) (0)
- Origin of the Supernumerary Chromosome in Trisomy 21 (2008) (0)
- Subject Index Vol. 92, 2001 (2001) (0)
- [Chromosome abnormalities: known risk factors]. (1980) (0)
- [FGF gene family and their role in human tumors]. (1988) (0)
- A new human brain cDNA molecule: assignment to chromosome 11q21-q23.1 and description of two polymorphisms studied by the polymerase chain reaction (1993) (0)
- Transmission of mental retardation with fragile X site by two normal transmitter brothers. (1991) (0)
- Subject Index Vol. 62, 1993 (1993) (0)
- S-Laminin gene (Lams) maps to F1 band of mouse Chromosome 9 (1994) (0)
- [Acquired idiopathic sideroblastic anemia: three cases with the same supplemental chromosome marker (47 Mar+)]. (1977) (0)
- Assignment1 of the centrosomal protein 110 gene (Cep110) to mouse chromosome bands 2B–C1 by in situ hybridization (2000) (0)
- [Individual variability of associations between acrocentrics (author's transl)]. (1981) (0)
- The 36th American Cytogenetics Conference (2000) (0)
- retardation2.3) and non-syndromic mental a female patient with an X;autosome translocation ) gene in ZNF741 ( KLF8 Abnormal expression of the (2008) (0)
- [Reciprocal translocation at the origin of a Robertsonian translocation 15;22 by the loss of a metacentric chromosome. Genetic counseling]. (1984) (0)
- Comparative mapping of the prostaglandin-D-synthase and other lipocalin genes in human and mouse chromosomes (1996) (0)
- Mouse alpha 1 type V collagen gene maps to the [A2-B] region of chromosome 2. (1993) (0)
- Molecular cloning, cDNA analysis, and localization of a monomer of the N-acetylglucosamine-specific receptor of the thyroid, NAGR1, to chromosome 19p13.3-13.2. (1995) (0)
- Contents, Vol. 65, 1994 (1994) (0)
- [Subacute myeloid leukemia with the Philadelphia chromosome and supplementary translocation: 9-12]. (1977) (0)
- Contribution of High-Resolution Banding and In Situ Hybridization to Clinical Cytogenetic Diagnosis (1987) (0)
- [Osteomyelosclerosis with hepatosplenic myeloid metaplasia associated with trisomy 8]. (1977) (0)
- Subject Index, Vol. 79, 1997 (1997) (0)
- Subject Index, Vol. 79, 1997 (1997) (0)
- Subject Index Vol. 63, 1993 (1993) (0)
- [Value of fluorescence for the identification of human chromosomes]. (1972) (0)
- Subject Index Vol. 87, 1999 (2000) (0)
- The Male Factor in Aid Requests: 558 Cases (1980) (0)
- Genetic Control of Diabetes Progression the islets ; after a substantial delay , destruction of the (1997) (0)
- [Structural abnormalities of the Y chromosome. Observations in ten cases]. (1979) (0)
- [Encephalopathy related to X fragility: neither inactivation nor deletion of the distal fragment q28 to qter. Enzymatic and morphometric evidence]. (1983) (0)
- Contents, Vol. 79, 1997 (1997) (0)
- Isolation and characterization of human cDNAs and genomic DNAs encoding alpha-4(IV) and alpha-6(IV) chains reveal the presence of a distinct subclass of collagen IV genes. (1994) (0)
- [Diagnosis of minor chromosome modifications by molecular cytogenetics]. (1989) (0)
- Mapping ofDNAmarkers close tothefragile site onthehumanX chromosome atXq27.3 (1987) (0)
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