Thomas B. Shows

Q: What Schools Are Affiliated With Thomas B. Shows

Thomas B. Shows is affiliated with the following schools: Yale University, Albert Einstein College of Medicine, University of Illinois College of Medicine, University of Chicago, Georgetown University, Kyoto University, University of Oulu

Thomas B. Shows's AcademicInfluence.com Rankings

Thomas B. Shows

Biology

#6325

World Rank

#9013

Historical Rank

Cell Biology

#196

World Rank

#203

Historical Rank

Molecular Biology

#637

World Rank

#652

Historical Rank

Neuroscience

#759

World Rank

#791

Historical Rank

biology Degrees

Download Badge

Biology

Thomas B. Shows's Degrees

PhD Molecular Biology University of California, San Francisco
Bachelors Biology Stanford University

Similar Degrees You Can Earn

Best Online Bachelor's in Biology 2026

Why Is Thomas B. Shows Influential?

(Suggest an Edit or Addition)

(See a Problem?)

Thomas B. Shows'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 zinc finger-encoding gene coregulated with c-fos during growth and differentiation, and after cellular depolarization (1988) (1211)
cDNA sequence and chromosomal localization of human platelet-derived growth factor A-chain and its expression in tumour cell lines (1986) (715)
Identification of a new endothelial cell growth factor receptor tyrosine kinase. (1991) (574)
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. (1999) (455)
Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues. (1988) (397)
Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein. (1988) (393)
Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma. (1989) (357)
Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome. (1990) (351)
Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogene-like sequence (GLUT6). (1990) (341)
Enhanced levels of insulin-like growth factor messenger RNA in human colon carcinomas and liposarcomas. (1986) (317)
tyk2, prototype of a novel class of non-receptor tyrosine kinase genes. (1990) (307)
Nonspecific integration of the HTLV provirus genome into adult T-cell leukaemia cells (1984) (286)
Molecular cloning, sequencing, and mapping of EGR2, a human early growth response gene encoding a protein with "zinc-binding finger" structure. (1988) (272)
Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues (1994) (260)
High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization. (1983) (251)
A truncated laminin chain homologous to the B2 chain: structure, spatial expression, and chromosomal assignment (1992) (246)
EGR3, a novel member of the Egr family of genes encoding immediate-early transcription factors. (1991) (227)
NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia. (1998) (214)
Brn-3b: a POU domain gene expressed in a subset of retinal ganglion cells (1993) (212)
Rearrangement and overexpression of D11S287E, a candidate oncogene on chromosome 11q13 in benign parathyroid tumors. (1991) (211)
Deletion in chromosome 11p associated with a hepatitis B integration site in hepatocellular carcinoma. (1985) (201)
Positional cloning of a gene involved in hereditary multiple exostoses. (1996) (191)
Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7 (1985) (187)
Human substance P receptor (NK-1): organization of the gene, chromosome localization, and functional expression of cDNA clones. (1991) (177)
Mapping of genes for the human C5a receptor (C5AR), human FMLP receptor (FPR), and two FMLP receptor homologue orphan receptors (FPRH1, FPRH2) to chromosome 19. (1992) (177)
Localization of insulin-like growth factor genes to human chromosomes 11 and 12 (1984) (172)
Mapping, genomic organization and promoter analysis of the human prostate-specific membrane antigen gene. (1998) (168)
Mapping the human genome, cloned genes, DNA polymorphisms, and inherited disease. (1982) (168)
cDNA cloning and chromosomal assignment of the gene encoding endothelin 3. (1989) (168)
The prolactin gene is located on chromosome 6 in humans. (1981) (166)
Structural organization and chromosomal assignment of the gene encoding endothelin. (1989) (163)
International system for human gene nomenclature (1979) ISGN (1979). (1979) (161)
Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus. (1997) (155)
Genes for growth hormone, chorionic somatommammotropin, and growth hormones-like gene on chromosome 17 in humans. (1980) (149)
Human immune interferon gene is located on chromosome 12 (1983) (148)
Cloning of human lysyl hydroxylase: complete cDNA-derived amino acid sequence and assignment of the gene (PLOD) to chromosome 1p36.3----p36.2. (1992) (144)
A group of type I keratin genes on human chromosome 17: characterization and expression (1988) (142)
Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. (1990) (142)
Hepatitis B virus integration site in hepatocellular carcinoma at chromosome 17;18 translocation. (1986) (142)
The human neurokinin A (substance K) receptor. Molecular cloning of the gene, chromosome localization, and isolation of the cDNA from tracheal and gastric tissues. (1990) (142)
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). (1987) (138)
cDNA cloning and chromosomal assignment of the endothelin 2 gene: vasoactive intestinal contractor peptide is rat endothelin 2. (1991) (129)
Chromosomal localization and nucleoside diphosphate kinase activity of human metastasis-suppressor genes NM23-1 and NM23-2. (1993) (128)
Cloning of a novel tumor necrosis factor-alpha-inducible primary response gene that is differentially expressed in development and capillary tube-like formation in vitro. (1992) (124)
Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome. (1983) (123)
Human chromosomes 6 and 21 are required for sensitivity to human interferon gamma. (1987) (120)
Chromosome mapping and organization of the human beta-galactoside alpha 2,6-sialyltransferase gene. Differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells. (1993) (120)
Human, mouse, and rat calnexin cDNA cloning: identification of potential calcium binding motifs and gene localization to human chromosome 5. (1994) (119)
The human connexin gene family of gap junction proteins: distinct chromosomal locations but similar structures. (1991) (117)
Isolation and Characterization of a Novel Zinc-finger Protein with Transcriptional Repressor Activity (*) (1995) (117)
Interleukin-1 gene (IL1) assigned to long arm of human chromosome 2. (1986) (115)
Localization of the human prealbumin gene to chromosome 18. (1985) (115)
Cloning of the chromosome translocation breakpoint junction of the t(14;19) in chronic lymphocytic leukemia. (1987) (114)
Human nonmuscle myosin heavy chain mRNA: generation of diversity through alternative polyadenylylation. (1990) (113)
The insulin gene is located on chromosome 11 in humans (1980) (109)
Human beta-hexosaminidase alpha chain: coding sequence and homology with the beta chain. (1985) (109)
Cloning and chromosomal assignment of a human cDNA encoding a T cell- and natural killer cell-specific trypsin-like serine protease. (1988) (107)
Human islet amyloid polypeptide gene: complete nucleotide sequence, chromosomal localization, and evolutionary history. (1989) (106)
Cloning of human and mouse EBI1, a lymphoid-specific G-protein-coupled receptor encoded on human chromosome 17q12-q21.2. (1994) (106)
Leukocyte and fibroblast interferon genes are located on human chromosome 9. (1981) (104)
Bestrophin gene mutations in patients with Best vitelliform macular dystrophy. (1999) (103)
The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus (1986) (103)
Type I procollagen COOH-terminal proteinase enhancer protein: identification, primary structure, and chromosomal localization of the cognate human gene (PCOLCE). (1994) (101)
The human TTP protein: sequence, alignment with related proteins, and chromosomal localization of the mouse and human genes. (1991) (99)
Autosomal control of an electrophoretic variant of glucose-6-phosphate dehydrogenase in the mouse (Mus musculus). (1968) (97)
The orphan G-protein-coupled receptor-encoding gene V28 is closely related to genes for chemokine receptors and is expressed in lymphoid and neural tissues. (1995) (96)
Functional characterization of human nucleosome assembly protein-2 (NAP1L4) suggests a role as a histone chaperone. (1997) (95)
Human metallothionein genes are clustered on chromosome 16. (1984) (93)
New members of the chemokine receptor gene family (1996) (91)
Human chemotaxis receptor genes cluster at 19q13.3-13.4. Characterization of the human C5a receptor gene. (1993) (91)
Function of the lactate dehydrogenase B gene in mouse erythrocytes: evidence for control by a regulatory gene. (1968) (89)
Transformation associated p53 protein is encoded by a gene on human chromosome 17 (1985) (88)
Assignment of the β-glucuronidase structural gene to the pter→q22 region of chromosome 7 in man (1978) (87)
The Insulin Gene Is Located on the Short Arm of Chromosome 11 in Humans (1981) (87)
Linkage-disequilibrium mapping without genotyping (1998) (82)
Somatic cell genetic evidence for X-chromosome linkage of three enzymes in the mouse (1976) (82)
The human myristoylated alanine-rich C kinase substrate (MARCKS) gene (MACS). Analysis of its gene product, promoter, and chromosomal localization. (1991) (79)
Genes for beta chain of human T-cell antigen receptor map to regions of chromosomal rearrangement in T cells. (1985) (78)
Polymorphic Human Glucose Transporter Gene (GLUT) is on Chromosome 1p31.3→p35 (1987) (78)
Gastric inhibitory polypeptide: structure and chromosomal localization of the human gene. (1989) (77)
Characterization of a novel tumor necrosis factor-alpha-induced endothelial primary response gene. (1992) (76)
Variable numbers of pepsinogen genes are located in the centromeric region of human chromosome 11 and determine the high-frequency electrophoretic polymorphism. (1985) (73)
Phospholipase C-148: chromosomal location and deletion mapping of functional domains. (1988) (73)
Genetics of human-mouse somatic cell hybrids: linkage of human genes for lactate dehydrogenase-A and esterase-A 4 . (1972) (73)
Chromosomal locations of human tissue plasminogen activator and urokinase genes. (1985) (72)
GENETIC AND PHYLOGENETIC VARIATION IN THE DIFFERENT MOLECULAR FORMS OF MAMMALIAN ERYTHROCYTE CARBONIC ANHYDRASES * (1968) (72)
Malate Dehydrogenase: Evidence for Tetrameric Structure in Mus musculus (1968) (71)
Genetics of colon carcinogenesis in mice treated with 1,2-dimethylhydrazine. (1977) (71)
MAGOH interacts with a novel RNA-binding protein. (2000) (71)
Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain. (1998) (71)
Completion of the primary structure of the human type IV collagenase preproenzyme and assignment of the gene (CLG4) to the q21 region of chromosome 16. (1990) (70)
The gene for protein S maps near the centromere of human chromosome 3. (1988) (69)
A model system to study genomic imprinting of human genes. (1998) (68)
Human c-Ki-ras2 proto-oncogene on chromosome 12. (1983) (67)
Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16. (1991) (67)
Inherited Variant of Erythrocyte Carbonic Anhydrase in Micronesians from Guam and Saipan (1963) (66)
Human monocyte Arg-Serpin cDNA. Sequence, chromosomal assignment, and homology to plasminogen activator-inhibitor (1987) (66)
Two human relaxin genes are on chromosome 9. (1984) (66)
Structure and chromosomal localization of the human salivary mucin gene, MUC7. (1996) (65)
Erythrocyte Glucose-6-Phosphate Dehydrogenase in Caucasians: New Inherited Variant (1964) (65)
Structure and chromosomal location of the human CD6 gene: detection of five human CD6 isoforms. (1997) (64)
Human β-D-N-Acetylhexosaminidases A and B: Expression and Linkage Relationships in Somatic Cell Hybrids (1974) (64)
A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region. (1997) (63)
Transcriptional regulation of TSG6, a tumor necrosis factor- and interleukin-1-inducible primary response gene coding for a secreted hyaluronan-binding protein. (1993) (62)
The core polypeptide of cystic fibrosis tracheal mucin contains a tandem repeat structure. Evidence for a common mucin in airway and gastrointestinal tissue. (1990) (62)
Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa1 (2000) (62)
A novel gene constitutively expressed in human lymphoid cells is inducible with interferon-γ in myeloid cells (2004) (61)
The complete derived amino acid sequence of human lysyl oxidase and assignment of the gene to chromosome 5 (extensive sequence homology with the murine ras recision gene). (1992) (61)
Structural organization and chromosomal assignment of the gene encoding the human heparin-binding epidermal growth factor-like growth factor/diphtheria toxin receptor. (1993) (61)
Structure and chromosomal location of the human gene encoding cartilage matrix protein. (1990) (60)
Intrachromosomal genomic instability in human sporadic colorectal cancer measured by genome-wide allelotyping and inter-(simple sequence repeat) PCR. (2001) (59)
Report of the nomenclature committee and the 1989 catalog of mapped genes. (1989) (59)
The 1991 catalog of mapped genes and report of the nomenclature committee (Part 1 of 5) (1991) (58)
Three epidermal and one simple epithelial type II keratin genes map to human chromosome 12. (1991) (57)
Three genes that encode human β-galactoside α2,3-sialyltransferases. Structural analysis and chromosomal mapping studies (1995) (57)
Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22. (1986) (56)
Mitochondrial malate dehydrogenase and malic enzyme: Mendelian inherited electrophoretic variants in the mouse (1970) (55)
Clustering of leukocyte and fibroblast interferon genes of human chromosome 9. (1982) (55)
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci. (1988) (55)
A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23. (1996) (55)
Localization of beckwith‐wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5 (1994) (54)
Chromosomal locations of the human and mouse genes for precursors of epidermal growth factor and the beta subunit of nerve growth factor. (1985) (54)
The 1990 catalog of mapped genes and report of the nomenclature committee. (1990) (54)
The genes for the lipopolysaccharide binding protein (LBP) and the bactericidal permeability increasing protein (BPI) are encoded in the same region of human chromosome 20. (1993) (53)
Tenth International Workshop on Human Gene Mapping (1988) (53)
Assignment of the gene for methylthioadenosine phosphorylase to human chromosome 9 by mouse-human somatic cell hybridization. (1984) (53)
The 1985 Catalog of Mapped Genes and report of the Nomenclature Committee. (1985) (53)
Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22----q24.1, 11p15, and 4q25----q27, respectively. (1986) (52)
Cloning and expression of the murine gene and chromosomal location of the human gene encoding N-acetylglucosaminyltransferase I. (1992) (52)
Cloning of human heparan sulfate proteoglycan core protein, assignment of the gene (HSPG2) to 1p36.1----p35 and identification of a BamHI restriction fragment length polymorphism. (1991) (52)
Esterase genetics in Mus musculus: expression, linkage, and polymorphism of locus Es-2. (1969) (50)
Localization of human SAA gene(s) to chromosome 11 and detection of DNA polymorphisms. (1986) (49)
The human cystatin C gene (CST3) is a member of the cystatin gene family which is localized on chromosome 20. (1989) (48)
Assignment of the human prohibitin gene (PHB) to chromosome 17 and identification of a DNA polymorphism. (1991) (48)
Suppression of tumorigenicity in somatic cell hybrids. II. Human chromosomes implicated as suppressors of tumorigenicity in hybrids with Chinese hamster ovary cells. (1983) (47)
Molecular analysis of a chromosomal translocation, t(9;14)(p13;q32), in a diffuse large-cell lymphoma cell line expressing the Ki-1 antigen. (1990) (47)
Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders. (1986) (47)
Mapping of aminoacylase-1 and beta-galactosidase-A to homologous regions of human chromosome 3 and mouse chromosome 9 suggests location of additional genes. (1982) (47)
Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-ras 1, and beta-hemoglobin. (1985) (47)
Chromosomal localization of an SH2-containing tyrosine phosphatase (PTPN6). (1992) (47)
Genes encoding pancreatic polypeptide and neuropeptide Y are on human chromosomes 17 and 7. (1986) (47)
Polymorphic human somatostatin gene is located on chromosome 3. (1983) (47)
Argininosuccinic aciduria: assignment of the argininosuccinate lyase gene to the pter to q22 region of human chromosome 7 by bioautography. (1978) (46)
The proopiocortin (adrenocorticotropin/β-lipotropin) gene is located on chromosome 2 in humans (1981) (46)
The gene for human carbonic anhydrase II (CA2) is located at chromosome 8q22. (1987) (46)
Chromosomal localization of the human apoprotein CI gene and of a polymorphic apoprotein AII gene. (1984) (46)
Hereditary variation of erythrocytic 6-phosphogluconate dehydrogenase. (1966) (45)
Lysosomal and Microsomal Glucuronidase: Genetic Variant Alters Electrophoretic Mobility of Both Hydrolases (1974) (45)
Human X-Linked genes regionally mapped utilizing X-autosome translocations and somatic cell hybrids. (1975) (45)
ISBT Working Party on Terminology for Red Cell Surface Antigens (1982) (45)
Mouse and human homologues of the yeast origin of replication recognition complex subunit ORC2 and chromosomal localization of the cognate human gene ORC2L. (1996) (44)
Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996 (Part 1 of 3) (1996) (43)
GM1-gangliosidosis: Chromosome 3 assignment of theβ-galactosidase-A gene (βGALA) (1979) (43)
Tissue factor gene localized to human chromosome 1 (1pter----1p21). (1985) (43)
Phosphoglucomutase electrophoretic variants in the mouse (1969) (42)
Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8. (1983) (42)
Genomic organization and chromosomal assignment for a serine protease gene (CSPB) expressed by human cytotoxic lymphocytes. (1989) (41)
Human collagen gene COL5A1 maps to the q34.2----q34.3 region of chromosome 9, near the locus for nail-patella syndrome. (1992) (40)
Structure and chromosomal localization of the human thrombospondin gene. (1990) (40)
Mucolipidosis II and III. The genetic relationships between two disorders of lysosomal enzyme biosynthesis. (1983) (40)
Two chromosomal locations for human ornithine decarboxylase gene sequences and elevated expression in colorectal neoplasia. (1990) (40)
Biochemical polymorphisms in feral and inbred mice (Mus musculus) (1971) (39)
Standardized karyotype of deer mice, Peromyscus (Rodentia) (1977) (39)
International System for Human Gene Nomenclature (1979) ISGN (1979). (1980) (39)
Lysosomal Acid phosphatase deficiency: liver specific variant in the mouse. (1977) (39)
The mammalian homologue of mago nashi encodes a serum-inducible protein. (1998) (38)
The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14. (1992) (38)
Chromosomal organization and localization of the human urokinase inhibitor gene: perfect structural conservation with ovalbumin. (1990) (38)
Mucolipidosis III is genetically heterogeneous. (1982) (38)
The 1983 catalogue of mapped human genetic markers and report of the Nomenclature Committee. (1982) (38)
A high-resolution physical map of human chromosome 11. (1996) (37)
Lysosomal arylsulfatase deficiencies in humans: chromosome assignments for arylsulfatase A and B. (1979) (37)
Human fertilin β: Identification, characterization, and chromosomal mapping of an ADAM gene family member (1997) (36)
Assignment of the human small inducible cytokine A2 gene, SCYA2 (encoding JE or MCP-1), to 17q11.2-12: evolutionary relatedness of cytokines clustered at the same locus. (1991) (36)
Chromosome 1 localization of the human alpha-L-fucosidase structural gene with a homologous site on chromosome 2. (1986) (36)
Assignment of the pepsinogen gene complex (PGA) to human chromosome region 11q13 by in situ hybridization. (1986) (35)
Mannosidosis: assignment of the lysosomal alpha-mannosidase B gene to chromosome 19 in man. (1977) (35)
Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects. (1998) (34)
The 1979 catalog of human genes and chromosome assignments. (1979) (34)
Genetic mapping of the human polymeric immunoglobulin receptor gene to chromosome region 1q31----q41. (1988) (34)
The human T-cell leukemia virus-related endogenous sequence (HRES1) is located on chromosome 1 at q42. (1991) (34)
DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22. (1984) (33)
Genome-wide allelotyping indicates increased loss of heterozygosity on 9p and 14q in early age of onset colorectal cancer (1999) (32)
Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes. (1998) (32)
A chromosome 11 YAC library. (1993) (31)
The gene for human transforming growth factor α is on the short arm of chromosome 2 (1986) (31)
Regional assignment of human amylase (AMY) to p22 → p21 of chromosome 1 (1984) (31)
Complete amino acid sequence of human cartilage link protein (CRTL1) deduced from cDNA clones and chromosomal assignment of the gene. (1990) (31)
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis. (1976) (30)
The UPS locus encoding uroporphyrinogen I synthase is located on human chromosome 11. (1980) (30)
The human angiotensinase C gene (HUMPCP) maps to 11q14 within 700 kb of D11S901: a candidate gene for essential hypertension. (1997) (30)
The human mineralocorticoid receptor gene (MLR) is located on chromosome 4 at q31.2. (1989) (29)
Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7. (1988) (29)
Pks, a raf-related sequence in humans. (1986) (29)
Mapping of the genes for human endoplasmic reticular heat shock protein gp96/grp94 (1993) (28)
The 1988 catalog of mapped genes and report of the nomenclature committee. (1988) (27)
Sequential expression in the nervous system of C-MYB andVIP genes, located in human chromosomal region 6q24 (1987) (27)
Chromosome 1 localization of the gene for CD34, a surface antigen of human stem cells. (1990) (27)
A sequence homologous to Rous sarcoma virus v-src Is on human chromosome 20. (1983) (26)
Genetic heterogeneity of I-cell disease is demonstrated by complementation of lysosomal enzyme processing mutants. (1982) (26)
Heterogeneity of N-acetylglucosamine 1-phosphotransferase within mucolipidosis III. (1986) (26)
Generation of a full-length human perinatal myosin heavy-chain-encoding cDNA. (1990) (26)
Genetics of the large, external, transformation-sensitive (LETS) protein: assignment of a gene coding for expression of LETS to human chromosome 8. (1978) (26)
Human Facilitative Glucose Transporters (2001) (26)
A gene map of the Best's vitelliform macular dystrophy region in chromosome 11q12-q13.1. (1998) (25)
The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 1 of 4) (1987) (25)
Electrophoretic abnormalities of lysosomal enzymes in mucolipidosis fibroblast lines. (1977) (25)
A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13. (1997) (25)
Epidermal type I transglutaminase (TGM1) is assigned to human chromosome 14. (1991) (25)
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clones. (1990) (24)
Isolation of a human laminin B2 (LAMB2) cDNA clone and assignment of the gene to chromosome region 1q25----q31. (1988) (24)
Measurement of genetic heterogeneity by means of enzyme polymorphisms, in wild populations of the mouse. (1969) (24)
Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping (1990) (24)
Framework YAC contig anchored into a 3.2-Mb high-resolution physical map in proximal 11q13. (1997) (24)
Localization of the human gene allowing infection by gibbon ape leukemia virus to human chromosome region 2q11-q14 and to the homologous region on mouse chromosome 2 (1991) (23)
Human pancreatic Beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13 (1992) (23)
Abstracts of workshop presentations (Part 13 of 13) (1985) (23)
The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy. (1988) (22)
Chromosomal localization of the gene encoding the human DNA helicase RECQL and its mouse homologue. (1995) (22)
Four new DNA markers are assigned to the WAGR region of 11p13: isolation and regional assignment of 112 chromosome 11 anonymous DNA segments. (1988) (22)
Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7. (1985) (22)
Coronavirus 229E susceptibility in man-mouse hybrids is located on human chromosome 15 (1982) (22)
Assignment of a fibronection gene to human chromosome 2 using monoclonal antibodies. (1982) (22)
Exon‐intron organization, expression, and chromosomal localization of the human motilin gene (1989) (22)
The TCF8 gene encoding a zinc finger protein (Nil-2-a) resides on human chromosome 10p11.2. (1992) (22)
Human chromosomes which affect tumorigenicity in hybrids of diploid human with heteroploid human or rodent cells. (1978) (21)
Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridization. (1990) (21)
Chromosomal localization of the human diazepam binding inhibitor gene. (1988) (21)
Mapping chromosomes 1 and 2 employing a 1/2 translocation in somatic cell hybrids. (1975) (21)
Localization of the human eosinophil Charcot-Leyden crystal protein (lysophospholipase) gene (CLC) to chromosome 19 and the human ribonuclease 2 (eosinophil-derived neurotoxin) and ribonuclease 3 (eosinophil cationic protein) genes (RNS2 and RNS3) to chromosome 14. (1992) (21)
Localization of human type II procollagen gene (COL2A1) to chromosome 12 (1984) (20)
Synteny of Human Genes for Glutamic Oxalacetic Transaminase and Hexokinase in Somatic Cell Hybrids (1974) (20)
A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus. (1991) (20)
Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm. (1991) (20)
Complex MLL rearrangement in a patient with T‐cell acute lymphoblastic leukemia (1995) (20)
Interstrain somatic cell hybrids in the mouse. Chromosome and enzyme analyses. (1970) (20)
Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
Regional assignment of two genes of the human branched-chain α-keto acid dehydrogenase complex: The E1β gene (BCKDHB) to chromosome 6p21–22 and the E2 gene (DBT) to chromosome 1p31 (1991) (19)
Assignment of uroporphyrinogen decarboxylase (UROD) to the pter----p21 region of human chromosome 1. (1985) (19)
A 1.5-megabase physical map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13. (1996) (19)
Assignment of the human collagen α1(XIII) chain gene (COL13A1) to the q22 region of chromosome 10 (1989) (19)
The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation. (1990) (19)
Chromosome Mapping and Organization of the Human (2001) (19)
Molecular biology of the alpha-L-fucosidase gene and fucosidosis. (1987) (19)
Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes. (1998) (18)
The kinase insert domain receptor gene (KDR) has been relocated to chromosome 4q11-->q12. (1995) (18)
Assignment of a β-galactosidase gene (βGALA) to chromosome 3 in man (1978) (18)
Nomenclature for human homeobox genes. (1990) (18)
Contig maps and genomic sequencing identify candidate genes in the usher 1C locus. (1998) (18)
Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cells (1995) (17)
The human neurokinin A (substance K) receptor. Molecular cloning of the gene, chromosome localization, and isolation of cDNA from tracheal and gastric tissues. (1990) (17)
Localization of the human collagen gene COL7A1 to 3p21.3 by fluorescence in situ hybridization. (1993) (17)
Mapping and characterization of an X-linked processed gene related to MYCL1. (1989) (16)
Centennial of Wilhelm Waldeyer’s introduction of the term “chromosome” (1988) (16)
The human transaldolase gene (TALDO1) is located on chromosome 11 at p15.4-p15.5. (1997) (16)
The human basic fibroblast growth factor gene (FGFB) is assigned to chromosome 4q25. (1990) (16)
A gene on human chromosome 6 functions in assembly of tissue-specific adenosine deaminase isozymes. (1978) (16)
Assignment of hexosaminidase-B to chromosome 5, its segregation after diphtheria toxin selection, and the linkage of hexosaminidase-A, mannose phosphate isomerase, and pyruvate kinase (M2). (1976) (16)
Human fertilin beta: identification, characterization, and chromosomal mapping of an ADAM gene family member. (1997) (15)
Assignment of β-hexosaminidase A α-subunit to human chromosomal region 15q23→q24 (1991) (15)
Mapping AK1, ACONs, and AK3 to chromosome 9 in man employing and X/9 translocation and somatic cell hybrids. (1977) (15)
Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5. (1995) (15)
The mucolipidoses: identification by abnormal electrophoretic patterns of lysosomal hydrolases. (1981) (15)
A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs. (1991) (15)
Assignment of the human fibronectin structural gene to chromosome 2. (1986) (15)
Assignment of tyrosine-specific T-cell phosphatase to conserved syntenic groups on human chromosome 18 and mouse chromosome 18. (1992) (15)
The KDR gene maps to human chromosome 4q31.2----q32, a locus which is distinct from locations for other type III growth factor receptor tyrosine kinases. (1992) (14)
Glutathione-S-transferase gene mapped to chromosome 11 is GST3 not GST1 letter (1984) (14)
Assignment of the human phosphoserine phosphatase gene (PSP) to the pter leads to q22 region of chromosome 7. (1983) (14)
Mapping thyrotropin β subunit gene in man and mouse (1986) (14)
Assignment of alpha-galactosidase (alpha GAL) to the q22 leads to qter region of the X chromosome in man. (1978) (14)
Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type. (1997) (14)
HUMAN MONOCYTE ARG-SERPIN cDNA (1987) (14)
The 1981 catalogue of assigned human genetic markers and report of the nomenclature committee. (1982) (13)
Report of the Committee on Genetic Markers (1974) (13)
A complex genetic rearrangement in a t(10;14)(q24;q11) associated with T‐cell acute lymphoblastic leukemia (1992) (13)
Two nonallelic tRNAiMet genes are located in the p23 leads to q12 region of human chromosome 6. (1983) (13)
Abstracts of workshop presentations (Part 1 of 13) (1985) (13)
ML‐1 cell line lacks a germline MLL locus (1996) (13)
The 1979 catalog of human genes and chromosome assignments. (1980) (13)
Cloning of a Portion of the Chromosomal Gene and cDNA for Human β-Fodrin, the Nonerythroid Form of β-Spectrin (1993) (13)
The 1987 Catalog of mapped genes and report of the nomenclature committee. (1987) (13)
The polymorphic human α2-macroglobulin gene (A2M) is located in chromosome region 12p12.3→p13.3 (1988) (12)
Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes. (1984) (12)
Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes (1987) (12)
The gene for the human mast cell high-affinity IgE receptor alpha chain: chromosomal localization to Iq21-q23 and RFLP analysis. (1989) (12)
Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7 (2004) (12)
An HLA-DRα promoter DNA-binding protein is expressed ubiquitously and maps to human chromosomes 22 and 5 (2004) (12)
Fine assignment of beta-hexosaminidase A alpha-subunit on 15q23-q24 by high resolution in situ hybridization. (1990) (12)
The chromosome 11 gene map: genes for growth and development, Wilms' tumor deletions, and cancer chromosome breakpoints. (1986) (11)
Three genes that encode human beta-galactoside alpha 2,3-sialyltransferases. Structural analysis and chromosomal mapping studies. (1995) (11)
The gene for human transforming growth factor alpha is on the short arm of chromosome 2. (1986) (11)
Gene markers for mapping the human genome (1975) (11)
A 3-Mb contig from D11S987 to MLK3, a gene-rich region in 11q13. (1997) (11)
Characterization of two 11q23.3–11q24 deletions and mapping of associated anonymous DNA markers (1993) (11)
The tumor phenotype and the human gene map☆ (1983) (11)
The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication (2002) (11)
DNA-mediated cotransfer of unlinked mammalian cell markers into mouse L cells (1980) (11)
Comparative gene mapping of HPRT, G6PD, and PGK in man, mouse, and muntjac deer. (1976) (11)
Assignment1 of Ubiquilin2 (UBQLN2) to human chromosome Xp11.23→p11.1 by GeneBridge radiation hybrids (2000) (11)
Somatic cell genetics of adenosine deaminase expression and severe combined immunodeficiency disease in humans. (1980) (11)
Humanα2-macroglobulin gene is located on chromosome 12 (1985) (11)
Epstein-Barr virus: studies on the association of virus genome with human chromosomes in hybrid cells. (1975) (10)
Abstracts of workshop presentations (Part 9 of 13) (1985) (10)
Evolutionary evidence for a regulator gene controlling the lactate dehydrogenase B gene in rodent erythrocytes (1969) (10)
6-Hydroxydopamine sensitivity in mouse neuroblastoma and neuroblastoma x L-cell hybrids. (1974) (10)
A YAC contig spanning the ataxia-telangiectasia locus (groups A and C) at 11q22-q23. (1994) (10)
Assignment of cytoplasmic alpha-mannosidase (MANA) and confirmation of mitochondrial isocitrate dehydrogenase (IDHM) to the q11 leads to qter region of chromosome 15 in man. (1978) (10)
Assignment of a gene for uridine diphosphate galactose-4-epimerase to human chromosome 1 by somatic cell hybridization, with evidence for a regional assignment to 1pter yields 1p21. (1979) (10)
I-cell disease and pseudo-Hurler polydystrophy: heterozygote detection and characteristics of the altered N-acetyl-glucosamine-phosphotransferase in genetic variants. (1985) (10)
Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
The human HNP36 gene is localized to chromosome 11q13 and produces alternative transcripts that are not mutated in multiple endocrine neoplasia, type 1 (MEN I) syndrome. (1997) (10)
Growth characteristics of Burkitt somatic cell hybrids in vitro. (1973) (10)
Confirmation of the assignment of the gene for galactose-1-phosphate uridylyltransferase (E.C. 2.7.7.12) to human chromosome 9. (1979) (10)
Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
Genetics of chromosome 11: loci for pediatric and adult malignancies, developmental disorders, and other diseases. (1995) (9)
International System for Cytogenetic Nomenclature (ISCN) — guidelines on cancer cytogenetics (1990) (9)
Abstracts of workshop presentations (Part 12 of 13) (1985) (9)
Assignment of human asialoglycoprotein receptor gene (ASGR1) to chromosome 17p11-13. (1991) (9)
Genetics of human-mouse somatic cell hybrids: Linkage of human genes for isocitrate dehydrogenase and malate dehydrogenase (1972) (9)
Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1. (1993) (9)
Chromosomal assignment of the gene for the human beta 2-adrenergic receptor. (1983) (9)
A single copy subclone, p1-101, from cosmid 3-3B, defines three RFLPs on 10pter-q23 [HGM9 no. D10S4]. (1987) (9)
The 1991 catalog of mapped genes and report of the nomenclature committee (Part 5 of 5) (1991) (9)
Expression of human hexosaminidase-A phenotype depends on genes assigned to chromosomes 5 and 15. (1976) (9)
The Complete Derived Amino Acid Sequence of Human Lysyl Oxidase and Assignment of the Gene to Chromosomes 5 (1992) (9)
Assignment of the gene for human carbonic anhydrase VIII(CA8) to chromosome 8q11-->q12. (1995) (9)
Pigment-cell-specific genes from fibroblasts are transactivated after chromosomal transfer into melanoma cells (1994) (9)
Assignment of the gene for human intra-acrosomal protein SP-10 to the p12----q13 region of chromosome 11. (1991) (9)
Gene sequences coding for S-adenosylmethionine decarboxylase are present on human chromosome 6 and the X and are not amplified in colon neoplasia. (1988) (9)
Localization of genes coding for PGK, HPRT, and G6PD on the long arm of the X chromosome in somatic cell hybrids. (1975) (8)
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19. (1992) (8)
Assignment of the gene for β-glucuronidase (βGUS) to chromosome 7 in man (1976) (8)
Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization. (1975) (8)
The proopiocortin (adrenocorticotropin/beta-lipoprotein) gene is located on chromosome 2 in humans. (1981) (8)
The catalog of human genes and chromosome assignments. A report on human genetic nomenclature and genes that have been mapped in man. (1978) (8)
Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
Human genome organization of enzyme loci and metabolic diseases. (1983) (8)
Organization of rDNA spacer fragment variants among human acrocentric chromosomes in somatic cell hybrids. (1983) (8)
Assignment1 of TLL1 and TLL2, which encode human BMP-1/Tolloid-related metalloproteases, to chromosomes 4q32→q33 and 10q23→q24 and assignment of murine Tll2 to chromosome 19 (1999) (7)
A 5.5-Mb high-resolution integrated map of distal 11q13. (1997) (7)
Molecular analysis of a t(11;14)(q23;q11) from a patient with null‐cell acute lymphoblastic leukemia (1993) (7)
Synteny Relationships of β-D-N-Acetylhexosaminidase A and B in Somatic Cell Hybrids (1974) (7)
Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
Localization of the dihydrolipoamide branched-chain transacylase gene (DBT) of the human branched-chain keto acid dehydrogenase complex to chromosome 1. (1991) (7)
Human β-glucuronidase: Assignment of the structural gene to chromosome 7 using somatic cell hybrids (1977) (6)
Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
Assignment and linear order of human acid phosphatase-2, esterase A4, and lactate dehydrogenase A genes on chromosome 11. (1976) (6)
Immunoselective loss of parental h antigens by somatic reduction in an H-2 a/H-2 b hybrid mouse leukemia. (1975) (6)
Gene mapping data – recommendations for more efficient dissemination (1983) (6)
Assignment of peptidase S (PEPS) to chromosome 4 in man using somatic cell hybrids (1978) (6)
GENETICS, EXPRESSION, AND CHARACTERIZATION OF ISOZYMES IN SOMATIC CELL HYBRIDS (1975) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
Studies on the alpha-mannosidase (MANB), peptidase D (PEPD), and glucose phosphate isomerase (GPI) syntenic group on chromosome 19 in man. (1978) (6)
The amino acid substitution and some chemical properties of a variant human erythrocyte carbonic anhydrase: carbonic anhydrase Id-Michigan. (1967) (6)
The human ribonuclease/angiogenin inhibitor is encoded by a gene mapped to chromosome 11p15.5, within 90 kb of the HRAS protooncogene. (1992) (6)
Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
The adrenergic responsiveness of Down syndrome cells. (1982) (6)
A human chromosome 11 NotI end clone library. (1993) (6)
An (Xq+;9p–) Translocation Suggests the Assignment of G6PD, HPRT, PGK to the Long Arm of the X Chromosome in Somatic Cell Hybrids (1974) (6)
Genetics of the cell surface: Assignment of genes coding for external membrane proteins to human chromosomes 10 and 14 (1979) (6)
Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization. (1975) (5)
Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
Comparative structure, proximal promoter elements, and chromosome location of the human eosinophil major basic protein genes. (2001) (5)
Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996 (Part 2 of 3) (1996) (5)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
A t(11;12) 11q23 leukemic breakpoint that disrupts the MLL Gene (1993) (5)
Human alpha 2-macroglobulin gene is located on chromosome 12. (1985) (5)
Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996 (Part 3 of 3) (1996) (5)
Correlation of in vivo malignancy with in vitro properties of human-mouse hybrid cells. (1976) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Assignment of a molecular form of UDP glucose pyrophosphorylase (UGPP2) to chromosome 2 in man. (1978) (5)
The amino acid substitution and some chemical properties of a variant human erythrocyte carbonic anhydrase: Carbonic anhydrase IdMichigan (1967) (5)
alpha-L-fucosidase (alpha FUC) localized to the pter towards to p21 region of chromosome 1 in man. (1978) (4)
Calendar of Events: 1991 — 1992 (1991) (4)
Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
Third International Congress of Histochemistry and Cytochemistry (1968) (4)
Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
Complementation of the Cellular A-T Phenotype by Gene Transfer. (1993) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
The polymorphic human alpha 2-macroglobulin gene (A2M) is located in chromosome region 12p12.3----p13.3. (1988) (4)
Genetics of cell fusion: Human chromosome 10 assignment of a gene(FUSE) that promotes polykaryocyte formation (1979) (4)
UDP-N-acetylglucosamine: lysosomal enzyme precursor N-acetylglucosamine-1-phosphate transferase activities in human ovarian tumor tissue and some transformed cell lines. (1987) (4)
Control of lysosomal acid phosphatase expression in man-mouse cell hybrids (1974) (4)
Human beta-D-N-acetylhexosaminidases A and B: expression and linkage relationships in somatic cell hybrids. (1974) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
Chromosomal assignment of the heparin-binding cytokine genes MDK and PTN in mouse and man. (1995) (4)
Gene markers for mapping the human genome. The 1974 listing. (1975) (3)
Gene transfer and gene mapping in mammalian cells in culture (2007) (3)
Segregation of esterase-D and adenine phosphoribosyl transferase in somatic cell hybrids: gene linkage or chromosome association? (1975) (3)
Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin. (1993) (3)
Human β-galactosidase and α-neuraminidase deficient mucolipidosis: Genetic complementation analysis of the neuraminidase deficiency (2004) (3)
Correction of mucolipidosis III in vitro by gene transfer. (1993) (3)
Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
Localization of the human uridine monophosphate kinase gene to the p21→pter region of chromosome 1 (1976) (3)
Linkage of Agt and Actsk-1 to distal mouse Chromosome 8 loci: a new conserved linkage (2004) (3)
Assignment of a beta-galactosidase gene (beta GALA) to chromosome 3 in man. (1978) (3)
Human beta-glucuronidase: assignment of the structural gene to chromosome 7 using somatic cell hybrids. (1977) (3)
Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
Assignment of the human collagen alpha 1 (XIII) chain gene (COL13A1) to the q22 region of chromosome 10. (1989) (3)
Regional assignment of two genes of the human branched-chain alpha-keto acid dehydrogenase complex: the E1 beta gene (BCKDHB) to chromosome 6p21-22 and the E2 gene (DBT) to chromosome 1p31. (1991) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Relationship between H1 histone phosphorylation and genome replication in a mouse-Chinese hamster somatic cell hybrid. (1983) (3)
Abstracts of workshop presentations (Part 11 of 13) (1985) (3)
Gene assignment of alpha-fucosidase and glucose dehydrogenase to the p21 leads to pter region of chromosome 1 in man. (1978) (3)
Assignment of beta-hexosaminidase A alpha-subunit to human chromosomal region 15q23----q24. (1991) (3)
Assignment of the glyoxalase II gene (HAGH) to human chromosome 16 (1981) (3)
Mapping of the mouse anonymous DNA fragment, D16Ros2, to human Chromosome 3 (2004) (2)
Abstracts of workshop presentations (Part 4 of 13) (1985) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
Calendar of Events 1992 (1992) (2)
Fused cells. (1977) (2)
Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
Abstracts of the 8th International Meeting (1999) (2)
Site Specific Mapping of Chromosome 21 Gene Probes and the Study of Down Syndrome (1987) (2)
GM1-gangliosidosis: chromosome 3 assignment of the beta-galactosidase-A gene (beta GALA). (1979) (2)
Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1→p14 (2001) (2)
Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
Mapping thyrotropin beta subunit gene in man and mouse. (1986) (1)
Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
Abstracts of the 12th European Colloquium on Cytogenetics of Domestic Animals (1996) (1)
Mapping Tissue Plasminogen Activator and Urokinase Genes to Human Chromosomes (1985) (1)
Alexander F. Zakharov (1986) (1)
Mucolipidosis III is genetically heterogeneous ( pseudo-Hurler polydystrophy / somatic cell genetics / complementation analysis ) (1)
Localization of genes coding for PGK, HPRT, and G6PD on the long arm of the X chromosome in somatic cell hybrids. (1975) (1)
Workshop on mapping by somatic cell hybridization. (1982) (1)
Cell Hybridization and the 24 Human Gene Maps (1986) (1)
Abstracts of workshop presentations (Part 5 of 13) (1985) (1)
Fine Assignment of 3-Hexosaminidase A ar-Subunit on 15823-q 24 by High Resolution In Situ Hybridization (2006) (1)
Expression of human hexosaminidase-A phenotype depends on genes assigned to chromosomes 5 and 15. (1976) (1)
Assignment of the gene for beta-glucuronidase (beta-GUS) to chromosome 7 in man. (1976) (1)
Phyllis J. McAlpine, Ph.D., 1941–98: In Memoriam (1999) (1)
Abstracts of workshop presentations (Part 6 of 13) (1985) (1)
Gastric Inhibitory Polypeptide: Structure and ChromosomalLocalization of the Human Gene (2008) (1)
Identifying and Isolating Breast Cancer Associated Genes on Chromosome 11. (1995) (1)
Abstracts of workshop presentations (Part 7 of 13) (1985) (1)
Subject Index Vol. 53, 1990 (1990) (1)
Abstracts of workshop presentations (Part 2 of 13) (1985) (1)
Instructions for the preparation of gene mapping reports (1995) (1)
Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
CpG island clones for Chromosome 11p—a resource for mapping and gene identification (1995) (1)
Genetic control and characterization of several polymophic enzyme systems in mus musculus. Abstr. (1968) (1)
Genes for two homologous G-protein α subunits map to different human chromosomes (1987) (1)
Subject Index Vol. 94, 2001 (2001) (1)
Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
Contents Vol. 55, 1990 (1990) (1)
Assignment and linear order of human acid phosphatase-2, esterase A4, and lactate dehydrogenase A genes on chromosome 11. (1976) (1)
Assignment of the human integral transmembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridization and YAC mapping. (1996) (1)
Assignment of the beta-glucuronidase structural gene to the pter leads to q22 region of chromosome 7 in man. (1978) (1)
Subject Index Vol. 60, 1992 (1992) (0)
Subject index Vol. 40, 1985 (1985) (0)
Report of the nomenclature committee and the 1989 catalog of mapped genes (Part 3 of 3) (1989) (0)
Genetic and physical mapping of the Nijmegen Breakage Syndrome gene region at 8q21 (1998) (0)
Contents, Vol. 37, 1984 (1984) (0)
Subject Index Vol. 42, 1986 (1986) (0)
The 1990 catalog of mapped genes and report of the nomenclature committee (Part 3 of 4) (1990) (0)
Assignment of hexosaminidase-B to chromosome 5, its segregation after diphtheria toxin selection, and the linkage of hexosaminidase-A, mannose phosphate isomerase, and pyruvate kinase (M2). (1976) (0)
Contents, Vol. 53, 1990 (1990) (0)
Proceedings: Report of the Committee on Genetic Markers. Gene markers for mapping the human genome. (1974) (0)
Sporadic colorectal carcinoma microdissection: a novel laboratory technique to identify tumor suppressor genes1 (1999) (0)
Catalog of mapped human gene markers. (1980) (0)
The 1990 catalog of mapped genes and report of the nomenclature committee (Part 2 of 3) (1990) (0)
Gene assignment of a polykaryocytosis promoter (FUSE) to chromosome 10 in man. (1978) (0)
Human beta-galactosidase and alpha-neuraminidase deficient mucolipidosis: genetic complementation analysis of the neuraminidase deficiency. (1982) (0)
757 CHROMOSOME MAPPING OF HUMAN GENES BY GENE PURIFICATION SOMATIC CELL HYBRIDIZATION AND RESTRICTION ENZYME ANLAYSIS (1981) (0)
Editorial help (2004) (0)
Third International Congress of Histochemistry and Cytochemistry: August 18–22, 1968, New York, N.Y. (1968) (0)
GENE TRANSFER AND GENE MAPPING IN MAMMALIAN (2016) (0)
Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
Assignment of the gene for beta-glucuronidase (betaGUS) to chromosome 7 in man. (1976) (0)
Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
Contents Vol. 94, 2001 (2002) (0)
The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 3 of 4) (1987) (0)
Subject Index Vol. 32, 1982 (1982) (0)
Phyllis J. McAlpine, PhD, 1941-98: In memoriam - Obituary (1999) (0)
Subject Index Vol. 25, 1979 (1979) (0)
Characterization of a Polymorphic Human Apoprotein (APO) AII Gene: Chromosomal Localization of the APO AII and APO CI Genes and of a Probable High Density Lipoprotein Regulator Locos (1985) (0)
Mono clonal antibodies to human fibronectin detect poly peptide antigens encoded on human chromosome 2 (1981) (0)
Index by Keyword (1989) (0)
Subject Index Vol. 56, 1991 (1991) (0)
Localization of the human uridine monophosphate kinase gene to the p21 leads to pter region of chromosome 1. (1976) (0)
Subject Index Vol. 44, 1987 (1987) (0)
Contents, Vol. 44, 1987 (1987) (0)
Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
Subject Index Vol. 16, 1976 (1976) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
The 1991 catalog of mapped genes and report of the nomenclature committee (Part 4 of 5) (1991) (0)
HumanO-D-N-Acetylhexosaminidases A andB:Expression andLinkage Relationships inSomatic CellHybrids (GM2gangliosidosis/lysosomal enzymes/anti-hexosaminidase sera/electrophoresis) (1974) (0)
Gene markers for mapping the human genome. The 1974 listing. (1975) (0)
Localization of the human uridine monophosphate kinase gene to the p21 leads to pter region of chromosome 1. (1976) (0)
Letter from Thomas B. Shows to Victor A. McKusick (1976) (0)
HumanX-Linked GenesRegionally MappedUtilizing X-Autosome Translocations andSomatic CellHybrids (1975) (0)
GenesfromFibroblasts AreTransactivated after Chromosomal Transfer intoMelanomaCells (1994) (0)
The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 4 of 4) (1987) (0)
Contents, Vol. 32, 1982 (1982) (0)
Abstracts of workshop presentations (Part 8 of 13) (1985) (0)
Genetic variation in wild and inbred populations of mus musculus. Abstr. (1968) (0)
Mapping chromosomes 1 and 2 employing a 1/2 translocation in somatic cell hybrids. (1975) (0)
What's in a name? (1990) (0)
Title Page / Table of Contents / Abstracts (1991) (0)
Author Index / Subject Index Vol. 49, 1988 (1988) (0)
Subject Index Vol. 41, 1986 (2004) (0)
Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
Erratum: A 1.5-megabase physical map encompassing the Multiple Endocrine Neoplasia type-1 (MEN1) locus on chromosome 11q13 (Genomics (1996) Volume 38 (pp. 166-173)) (1997) (0)
The 1991 catalog of mapped genes and report of the nomenclature committee (Part 3 of 5) (1991) (0)
Subject Index Vol. 22, 1978 (1978) (0)
Index by Abstract Number (1989) (0)
The 1990 catalog of mapped genes and report of the nomenclature committee (Part 4 of 4) (1990) (0)
The 1991 catalog of mapped genes and report of the nomenclature committee (Part 2 of 5) (1991) (0)
Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
Abstracts of workshop presentations (Part 10 of 13) (1985) (0)
Segregation of esterase-D and adenine phosphoribosyl transferase in somatic cell hybrids: gene linkage or chromosome association? (1975) (0)
Primary structure of the human laminin α2 (Am, Merosin) chain, chromosomal assignment and expression of α2 and α1 chains in human fetal tissues (1994) (0)
Comparative gene mapping of HPRT, G6PD, and PGK in man, mouse, and muntjac deer. (1976) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
The 1981 catalogue of assigned human genetic markers and report of the nomenclature committee. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (0)
Samuel A. Latt, 1938–1988 (1988) (0)
Report of the nomenclature committee and the 1989 catalog of mapped genes (Part 2 of 3) (1989) (0)
Proceedings: Synteny relationships of beta-D-N-acetylhexosaminidase A and B in somatic cell hybrids. (1974) (0)
273 Comparison of structure and chromosome location of the human eosinophil major basic protein genes (2000) (0)
Proceedings: Synteny of human genes for glutamic oxalacetic transaminase and hexokinase in somatic cell hybrids. (1974) (0)
References to the committee reports (1975) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
Subject index Vol. 46, 1987 (1987) (0)
Contents, Vol. 56, 1991 (2004) (0)

This paper list is powered by the following services:

What Schools Are Affiliated With Thomas B. Shows?

Thomas B. Shows is affiliated with the following schools:

Thomas B. Shows's Academic­Influence.com Rankings

Thomas B. Shows's Degrees

Similar Degrees You Can Earn

Why Is Thomas B. Shows Influential?

Thomas B. Shows's Published Works

Published Works

What Schools Are Affiliated With Thomas B. Shows?

Thomas B. Shows's AcademicInfluence.com Rankings