Peter Marynen

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Peter Marynen is affiliated with the following schools: University of Lausanne, Ghent University, KU Leuven, University of Perugia, University of Salamanca

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Peter Marynen'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

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. (2005) (2933)
A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. (2003) (1709)
Allele-specific copy number analysis of tumors (2010) (934)
Gene prioritization through genomic data fusion (2006) (924)
The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomas. (1999) (718)
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males. (2005) (615)
Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia. (1997) (537)
Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants. (2005) (484)
Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia (2004) (432)
Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports (2006) (399)
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype (2007) (398)
T cell antigen receptor stimulation induces MALT1 paracaspase–mediated cleavage of the NF-κB inhibitor A20 (2008) (380)
Genomic imbalances including amplification of the tyrosine kinase gene JAK2 in CD30+ Hodgkin cells. (2000) (297)
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation (1999) (290)
Transformation of hematopoietic cell lines to growth‐factor independence and induction of a fatal myelo‐ and lymphoproliferative disease in mice by retrovirally transduced TEL/JAK2 fusion genes (1998) (280)
Identification of novel fusion partners of ALK, the anaplastic lymphoma kinase, in anaplastic large‐cell lymphoma and inflammatory myofibroblastic tumor (2002) (269)
Efficacy of the Kinase Inhibitor SU11248 against Gastrointestinal Stromal Tumor Mutants Refractory to Imatinib Mesylate (2006) (267)
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplasic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation (2008) (266)
Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia (2007) (266)
The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia. (1996) (258)
Molecular cloning of a phosphatidylinositol-anchored membrane heparan sulfate proteoglycan from human lung fibroblasts (1990) (258)
PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRα-induced myeloproliferative disease. (2003) (234)
A20 Negatively Regulates T Cell Receptor Signaling to NF-κB by Cleaving Malt1 Ubiquitin Chains1 (2009) (222)
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation. (2008) (205)
Rapid DNA typing of class II HLA antigens using the polymerase chain reaction and reverse dot blot hybridization. (1993) (200)
The product of the t(11;18), an API2-MLT fusion, marks nearly half of gastric MALT type lymphomas without large cell proliferation. (2000) (200)
MALT1 is deregulated by both chromosomal translocation and amplification in B-cell non-Hodgkin lymphoma. (2003) (197)
Eighth International Workshop on Human Gene Mapping (1984) (195)
Prediction of Resistance to Small Molecule FLT3 Inhibitors (2004) (192)
Detection of genomic copy number changes in patients with idiopathic mental retardation by high‐resolution X‐array‐CGH: important role for increased gene dosage of XLMR genes (2007) (187)
ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma. (2003) (181)
TP53 mutations are frequent in malignant NFI tumors (1994) (179)
Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias (2004) (178)
Recombination hotspot in NF1 microdeletion patients. (2001) (173)
Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis (2005) (168)
Partial primary structure of the 48- and 90-kilodalton core proteins of cell surface-associated heparan sulfate proteoglycans of lung fibroblasts. Prediction of an integral membrane domain and evidence for multiple distinct core proteins at the cell surface of human lung fibroblasts. (1989) (168)
Molecular cloning of amphiglycan, a novel integral membrane heparan sulfate proteoglycan expressed by epithelial and fibroblastic cells (1992) (159)
FOXP1, a gene highly expressed in a subset of diffuse large B-cell lymphoma, is recurrently targeted by genomic aberrations (2005) (153)
The Dark Side of EGFP: Defective Polyubiquitination (2006) (151)
Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesis. (2000) (150)
Fusion of EML1 to ABL1 in T-cell acute lymphoblastic leukemia with cryptic t(9;14)(q34;q32). (2005) (149)
Fusion of ETV6 to MDS1/EVI1 as a result of t(3;12)(q26;p13) in myeloproliferative disorders. (1997) (148)
CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior. (2003) (138)
Spatial and temporal changes in the expression of fibroglycan (syndecan-2) during mouse embryonic development. (1993) (137)
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. (2008) (135)
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1. (1999) (129)
Activity of Dasatinib, a Dual SRC/ABL Kinase Inhibitor, and IPI-504, a Heat Shock Protein 90 Inhibitor, against Gastrointestinal Stromal Tumor–Associated PDGFRAD842V Mutation (2008) (125)
Genetic insights in the pathogenesis of T-cell acute lymphoblastic leukemia. (2005) (125)
Atonal homolog 1 Is a Tumor Suppressor Gene (2009) (125)
A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias (2005) (124)
Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map (2004) (121)
Activation of FIP1L1-PDGFRα requires disruption of the juxtamembrane domain of PDGFRα and is FIP1L1-independent (2006) (118)
FIP1L1-PDGFRα D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRα T674I eosinophilic leukemia with single agent sorafenib (2009) (117)
Genomic organization of TEL: the human ETS-variant gene 6. (1996) (115)
ALK‐ATIC fusion in urinary bladder inflammatory myofibroblastic tumor (2003) (113)
Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2. (1996) (113)
Sorafenib is a potent inhibitor of FIP1L1-PDGFRα and the imatinib-resistant FIP1L1-PDGFRα T674I mutant (2006) (112)
Recurrent rearrangement of the Ewing's sarcoma gene, EWSR1, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia. (2002) (111)
TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13). (1995) (109)
Translocation t(11;18) absent in early gastric marginal zone B-cell lymphoma of MALT type responding to eradication of Helicobacter pylori infection. (2000) (108)
cIAP2 is a ubiquitin protein ligase for BCL10 and is dysregulated in mucosa-associated lymphoid tissue lymphomas. (2005) (107)
Identification of the critical region of 12p over-representation in testicular germ cell tumors of adolescents and adults (1998) (106)
JAK2 rearrangements, including the novel SEC31A-JAK2 fusion, are recurrent in classical Hodgkin lymphoma. (2009) (106)
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis. (2005) (105)
The NPM-ALK and the ATIC-ALK fusion genes can be detected in non-neoplastic cells. (2001) (105)
Unequal meiotic crossover: a frequent cause of NF1 microdeletions. (2000) (104)
The ability of sorafenib to inhibit oncogenic PDGFRbeta and FLT3 mutants and overcome resistance to other small molecule inhibitors. (2007) (104)
Characterization of glypican-5 and chromosomal localization of human GPC5, a new member of the glypican gene family. (1997) (98)
Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21). (1996) (97)
The EOL-1 cell line as an in vitro model for the study of FIP1L1-PDGFRA-positive chronic eosinophilic leukemia. (2004) (94)
ALK-positive large B-cell lymphomas with cryptic SEC31A-ALK and NPM1-ALK fusions (2010) (93)
Translocations t(11;18)(q21;q21) and t(14;18)(q32;q21) are the main chromosomal abnormalities involving MLT/MALT1 in MALT lymphomas (2003) (93)
Fusion of a novel gene, BTL, to ETV6 in acute myeloid leukemias with a t(4;12)(q11-q12;p13). (1999) (92)
Detection of t(11;18)(q21;q21) by interphase fluorescence in situ hybridization using API2 and MLT specific probes. (2000) (92)
Rapid detection of hypervariable regions by the polymerase chain reaction technique. (1990) (91)
Evidence for Co-Evolution between Human MicroRNAs and Alu-Repeats (2009) (90)
Report of the Third International Workshop on Human Chromosome 12 Mapping 1995. (1996) (89)
Evidence for position effects as a variant ETV6-mediated leukemogenic mechanism in myeloid leukemias with a t(4;12)(q11-q12;p13) or t(5;12)(q31;p13). (2002) (89)
Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion (2006) (87)
The receptor-binding domain of human alpha 2-macroglobulin. Isolation after limited proteolysis with a bacterial proteinase. (1986) (86)
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome. (1996) (85)
Copy-number gains of HUWE1 due to replication- and recombination-based rearrangements. (2012) (83)
X‐linked mental retardation: vanishing boundaries between non‐specific (MRX) and syndromic (MRXS) forms (2002) (82)
Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes. (1996) (81)
The Sp1 transcription factor gene (SP1) and the 1,25-dihydroxyvitamin D3 receptor gene (VDR) are colocalized on human chromosome arm 12q and rat chromosome 7. (1991) (81)
Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombination. (2009) (80)
GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome. (1998) (80)
Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR gene. (1993) (78)
A Novel TRAF6 Binding Site in MALT1 Defines Distinct Mechanisms of NF-κB Activation by API2·MALT1 Fusions* (2007) (77)
Coactivated platelet-derived growth factor receptor {alpha} and epidermal growth factor receptor are potential therapeutic targets in intimal sarcoma. (2010) (76)
A monoclonal antibody to a neo-antigen on alpha 2-macroglobulin complexes inhibits receptor-mediated endocytosis. (1981) (72)
Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions (1999) (72)
The FIP1L1-PDGFR&agr; kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia (2004) (72)
Differences in the distribution and nature of the interstitial telomeric (TTAGGG)n sequences in the chromosomes of the Giraffidae, okapai (Okapia johnstoni), and giraffe (Giraffa camelopardalis): evidence for ancestral telomeres at the okapi polymorphic rob(5;26) fusion site. (1996) (72)
Role of cardiac myocyte tissue factor in heart hemostasis (2007) (71)
Activation of FIP1L1-PDGFRalpha requires disruption of the juxtamembrane domain of PDGFRalpha and is FIP1L1-independent. (2006) (70)
Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies. (1998) (69)
Kinase activation and transformation by NUP214-ABL1 is dependent on the context of the nuclear pore. (2008) (68)
NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardation (2001) (68)
Computational methods for the detection of cis-regulatory modules (2009) (68)
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA. (2006) (68)
MCT8 mutation analysis and identification of the first female with Allan–Herndon–Dudley syndrome due to loss of MCT8 expression (2008) (67)
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases. (2005) (65)
Efficient male and female germline transmission of a human chromosomal vector in mice. (2001) (64)
Identification of Intellectual Disability Genes in Female Patients with a Skewed X‐Inactivation Pattern (2016) (64)
Sorafenib is a potent inhibitor of FIP1L1-PDGFRalpha and the imatinib-resistant FIP1L1-PDGFRalpha T674I mutant. (2006) (63)
Selective Expansion of Marginal Zone B Cells in Eμ-API2-MALT1 Mice Is Linked to Enhanced IκB Kinase γ Polyubiquitination (2006) (62)
MALT1 Auto-Proteolysis Is Essential for NF-κB-Dependent Gene Transcription in Activated Lymphocytes (2014) (62)
T-cell/histiocyte-rich large B-cell lymphoma shows transcriptional features suggestive of a tolerogenic host immune response (2010) (61)
Interstitial telomeric sequences at the junction site of a jumping translocation (1997) (60)
The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y. (1997) (59)
Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene. (1995) (56)
Construction and evaluation of a hncDNA library of human 12p transcribed sequences derived from a somatic cell hybrid. (1993) (56)
X chromosome array-CGH for the identification of novel X-linked mental retardation genes. (2005) (54)
Tenth International Workshop on Human Gene Mapping (1988) (53)
Characterization of a double homeodomain protein (DUX1) encoded by a cDNA homologous to 3.3 kb dispersed repeated elements. (1998) (53)
Relation of internal thioesters to conformational change and receptor-recognition site in alpha 2-macroglobulin complexes. (1982) (52)
Characterization of a helicase-like transcription factor involved in the expression of the human plasminogen activator inhibitor-1 gene. (1996) (52)
Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal allele. (1995) (51)
Submicroscopic deletions in 5q- associated malignancies. (2004) (51)
A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephew (1990) (51)
The Atonal Proneural Transcription Factor Links Differentiation and Tumor Formation in Drosophila (2009) (50)
Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS. (1995) (50)
Primary Structure and Gene Structure of Staphylokinase (1992) (50)
A deletion polymorphism in the human alpha-2-macroglobulin (A2M) gene. (1991) (49)
Resistance to tyrosine kinase inhibitors: calling on extra forces. (2005) (48)
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients (2003) (48)
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region (2007) (47)
Incorporation of dITP or 7-deaza dGTP during PCR improves sequencing of the product. (1993) (47)
ETV6 gene rearrangements in hematopoietic malignant disorders. (1996) (46)
The product of the t(11;18), an API2-MLT fusion, is an almost exclusive finding in marginal zone cell lymphoma of extranodal MALT-type. (2000) (46)
Structure of the MLT gene and molecular characterization of the genomic breakpoint junctions in the t(11;18)(q21;q21) of marginal zone B‐cell lymphomas of MALT type (2000) (46)
Detection of bacterial and mycoplasma contamination in cell cultures by polymerase chain reaction. (1992) (45)
Identification of a novel conserved human gene, TEGT. (1995) (44)
Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL (2007) (44)
The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberration in different hematological malignancies. (1996) (43)
MAPK phosphatase DUSP16/MKP-7, a candidate tumor suppressor for chromosome region 12p12–13, reduces BCR-ABL-induced transformation (2003) (43)
Selective expansion of marginal zone B cells in Emicro-API2-MALT1 mice is linked to enhanced IkappaB kinase gamma polyubiquitination. (2006) (42)
Activity of imatinib in systemic mastocytosis with chronic basophilic leukemia and a PRKG2-PDGFRB fusion (2008) (41)
A novel cryptic translocation t(12;17)(p13;p12–p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene (2003) (41)
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome. (1997) (40)
ModuleMiner - improved computational detection of cis-regulatory modules: are there different modes of gene regulation in embryonic development and adult tissues? (2008) (40)
Inhibition of intracellular proteolytic processing of soluble proproteins by an engineered alpha 2-macroglobulin containing a furin recognition sequence in the bait region. (1997) (39)
Primary structure of pregnancy zone protein. Molecular cloning of a full-length PZP cDNA clone by the polymerase chain reaction. (1991) (39)
Complex genomic rearrangement of ALK loci associated with integrated human Epstein-Barr virus in a post-transplant myogenic liver tumor. (2003) (39)
Genomic organization and evolution of the NF1 microdeletion region. (2004) (38)
A new subtype of pre-B acute lymphoblastic leukemia with t(5;12)(q31q33;p12), molecularly and cytogenetically distinct from t(5;12) in chronic myelomonocytic leukemia. (1997) (38)
A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p). (1999) (38)
Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome. (2002) (37)
Small chromosomal regions position themselves autonomously according to their chromatin class. (2017) (36)
A human homologue (BICD1) of the Drosophila bicaudal-D gene. (1997) (36)
Fusion of EML 1 to ABL 1 in T-cell acute lymphoblastic leukemia with cryptic t ( 9 ; 14 ) ( q 34 ; q 32 ) (2005) (35)
Importance of HLA-DRB1 and DQA1 genes and of the amino acid polymorphisms in the functional domain of DRβ1 chain in multiple sclerosis (1995) (34)
Interaction partners for human ZNF384/CIZ/NMP4--zyxin as a mediator for p130CAS signaling? (2006) (34)
CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients (2005) (34)
Telomere-independent homologue pairing and checkpoint escape of accessory ring chromosomes in male mouse meiosis (2003) (33)
NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance (2005) (33)
Structural organisation of the gene encoding the α-subunit of the human amiloride-sensitive epithelial sodium channel (1998) (32)
A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome (2007) (32)
Evidence for increased SOX3 dosage as a risk factor for X‐linked hypopituitarism and neural tube defects (2014) (31)
The epitopes of two complex-specific monoclonal antibodies, related to the receptor recognition site, map to the COOH-terminal end of human alpha 2-macroglobulin. (1986) (31)
Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35). (1996) (29)
e6-a2 BCR-ABL1 fusion in T-cell acute lymphoblastic leukemia (2005) (28)
Biallelic alterations of both ETV6 and CDKN1B genes in a t(12;21) childhood acute lymphoblastic leukemia case. (1996) (28)
Study of the possible association of HLA class II, CD4, and CD3 polymorphisms with schizophrenia. (1994) (27)
Translocation t(1;6)(p35.3;p25.2): a new recurrent aberration in ‘unmutated’ B-CLL (2005) (27)
Isolation and regional assignment of human chromosome 12p cDNAs. (1995) (27)
Complex variant Philadelphia translocations involving the short arm of chromosome 6 in chronic myeloid leukemia. (2002) (27)
Structure of the human alpha-2 macroglobulin gene and its promotor. (1992) (27)
Simultaneous screening for 11 mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex amplification and reverse dot-blot. (1992) (26)
Evidence for the existence of a pristanoyl-CoA oxidase gene in man. (1997) (26)
Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: a report including three novel translocations involving the TEL/ETV6 gene (1997) (26)
Genetic heterogeneity in Rieger eye malformation. (1994) (26)
Controlled transgene dosage and PAC-mediated transgenesis in mice using a chromosomal vector. (2003) (25)
Co‐amplification of the cystic fibrosis ΔF508 mutation with the HLA DQA1 sequence in single cell PCR: Implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosis (1993) (25)
A Novel TRAF6 binding site in MALT1 defines distinct mechanisms of NF-kappaB activation by API2middle dotMALT1 fusions. (2007) (25)
Differential splicing of COL4A5 mRNA in kidney and white blood cells: a complex mutation in the COL4A5 gene of an Alport patient deletes the NC1 domain. (1993) (25)
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemia (1999) (24)
Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability (2013) (24)
The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability (2013) (24)
Novel PORCN mutations in focal dermal hypoplasia (2009) (23)
Splenic marginal zone lymphoma-like features in API2-MALT1 transgenic mice that are exposed to antigenic stimulation. (2006) (23)
X-linked mental retardation and epigenetics (2006) (23)
FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells (2007) (22)
Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: Clinical study and mutation analysis of the NXF5 Gene (2003) (22)
Linkage analysis in three families with nonspecific X-linked mental retardation. (1996) (21)
Limited Expansion of the (CAG)n Repeat of the Huntington Gene: A Premutation (?) (1994) (21)
Receptor-mediated endocytosis of alpha 2macroglobulin-protease complexes by fibroblasts in culture. Competitive inhibition by bacitracin. (1981) (21)
Mapping of an ordered set of 14 cosmids to human chromosome 12p by two-color in situ hybridization. (1995) (20)
Charge reduction of zeolite Y through exchange with lanthanum ions: Intracrystalline oxide and hydroxide formation (1984) (20)
Human and rat chromosomal localization of two genes for 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase by analysis of somatic cell hybrids and in situ hybridization. (1991) (20)
Proteolysis at a lysine residue abolishes the recetor‐recognition site of α2‐Macroglobulin complexes (1982) (20)
A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12. (1995) (20)
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation (2014) (20)
Assignment of the human glypican gene (GPC1) to 2q35-q37 by fluorescence in situ hybridization. (1995) (20)
Chromosome healing of constitutional chromosome deletions studied by microdissection (1998) (20)
A20 Negatively Regulates T Cell Receptor (2009) (20)
Solubilization and affinity purification of the alpha 2-macroglobulin receptor from human fibroblasts. (1984) (19)
Regional mapping of the human NSP gene to chromosome region 14q21-->q22 by fluorescence in situ hybridization analysis. (1994) (19)
Cloning and characterization of the promoter region of the murine alpha-4 integrin subunit. (1994) (19)
CREBL2, a novel transcript from the chromosome 12 region flanked by ETV6 and CDKN1B. (1998) (18)
A cluster of α2-macroglobulin-related genes (α2M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an α2M pseudogene (1989) (17)
A new family of small, palmitoylated, membrane‐associated proteins, characterized by the presence of a cysteine‐rich hydrophobic motif (2001) (17)
Xp22.3; Yq11.2 chromosome translocation and its clinical manifestations. (2001) (16)
The gene for the alpha 4 subunit of the VLA-4 integrin maps to chromosome 2Q31-32. (1991) (16)
Immature teratoma of the pineal gland with isochromosome 12p (1997) (16)
Centennial of Wilhelm Waldeyer’s introduction of the term “chromosome” (1988) (16)
Activation of FIP 1 L 1-PDGFR requires disruption of the juxtamembrane domain of PDGFR and is FIP 1 L 1-independent (2006) (15)
Telomere length homeostasis and telomere position effect on a linear human artificial chromosome are dictated by the genetic background (2012) (15)
A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia (1997) (15)
Possible association of CD3 and CD4 polymorphisms with insulin‐dependent diabetes mellitus (IDDM) (1994) (15)
Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13). (2006) (15)
A form of non-specific mental retardation is probably caused by a microdeletion in a Belgian family (1996) (15)
Proteolysis of human alpha 2-macroglobulin without hydrolysis of the internal thiolesters or expression of the receptor recognition site. (1988) (14)
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome (1989) (14)
Mapping of structure-function relationships in proteins with a panel of monoclonal antibodies. A study on human alpha 2 macroglobulin. (1988) (14)
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia (2006) (14)
Detection and validation of copy number variation in X-linked mental retardation (2009) (14)
A rapid, semiautomated method for apolipoprotein E genotyping. (1993) (14)
Molecular Characterization of 12 p Abnormalities in Hematologic Malignancies : Deletion of K I P I , Rearrangement of TEL , and Amplification of CCND 2 (2002) (14)
FIP1L1-PDGFRalpha in hypereosinophilic syndrome and mastocytosis. (2004) (14)
Transition from EML1-ABL1 to NUP214-ABL1 positivity in a patient with acute T-lymphoblastic leukemia (2006) (13)
Stability of metal uncharged ligand complexes in ion exchangers. Part 1.—Quantitative characterization and thermodynamic basis (1977) (13)
Clinical study and haplotype analysis in two brothers with Partington syndrome. (2002) (13)
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia. (2007) (13)
Role of the alpha 2M-receptor in attachment and spreading of human fibroblasts. (1981) (13)
Auto-Ubiquitination-Induced Degradation of MALT1-API2 Prevents BCL10 Destabilization in t(11;18)(q21;q21)-Positive MALT Lymphoma (2009) (13)
dup(12)(q13→qter) in two t(14;18)‐negative follicular b‐non‐hodgkin's lymphomas (1992) (12)
Localization of the gene encoding the α2 subunit of the human VLA-2 receptor to chromosome 5q23-31 (1991) (12)
The Ion Exchange Adsorption of Alkylammonium Ions: An Alternative View (1977) (12)
Report of the fourth International Workshop in Human Chromosome 12 Mapping, 1997. (1997) (11)
A mouse monoclonal antibody to human alpha 2-macroglobulin (alpha 2M) crossreacts with alpha 2M from mouse: epitope mapping and characterization of subunit structure of murine alpha 2M. (1987) (11)
Cryptic translocation t(5;18) in familial mental retardation. (2000) (11)
Reversed dot-blotting in hybridoma screening and epitope mapping. A model study with human alpha 2-macroglobulin to select complex-specific monoclonal antibodies. (1986) (11)
Report and abstracts of the Second International Workshop on Human Chromosome 12 mapping 1994. New Haven, Connecticut, June 20-22, 1994. (1994) (11)
A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13). (1995) (10)
Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line. (2002) (10)
Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study. (1999) (10)
API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with MALT lymphomas (1999) (10)
Ovarian germ cell tumor with chromosome 12 anomaly but without i(12p). (1996) (10)
Microdissection and FISH investigations in acute myeloid leukemia: a step forward to full identification of complex karyotypic changes. (2000) (10)
Association of particular HLA class II alleles, haplotypes and genotypes with susceptibility to IDDM in the Belgian population (1994) (10)
Sorafenib is a potent inhibitor of FIP 1 L 1-PDGFR and the imatinib-resistant FIP 1 L 1-PDGFR T 674 I mutant (2006) (10)
Mapping of rat prostatic binding protein genes C1, C2, and C3 to rat chromosome 5 by in situ hybridization. (1988) (10)
Advances in Brief Prediction of Resistance to Small Molecule FLT 3 Inhibitors : Implications for Molecularly Targeted Therapy of Acute Leukemia (2004) (10)
Cellular transformation of NIH3T3 fibroblasts by CIZ/NMP4 fusions (2005) (9)
A novel fusion of the MALT1 gene and the microtubule‐associated protein 4 (MAP4) gene occurs in diffuse large B‐cell lymphoma (2006) (9)
Two cases of myeloid disorders and a t(8;12) (q12;p13). (2000) (9)
Increased and decreased relative risk for noninsulin‐dependent diabetes mellitus conferred by HLA class II and by CD4 alleles (1995) (9)
Malt1 self‐cleavage is critical for regulatory T cell homeostasis and anti‐tumor immunity in mice (2018) (9)
The novel t(11;12;18)(q21;q13;q21) represents a variant translocation of the t(11;18)(q21;q21) associated with MALT-type lymphoma (2002) (8)
Sporadic late onset ornithine transcarbamylase deficiency in a boy with somatic mosaicism for an intragenic deletion (1990) (8)
Differential splicing of COL4A5 mRNA in kidney and white blood cells: A complex mutation in the COL4A5 gene of an alport patient deletes the NC1 domain (1994) (8)
The genes coding for rat cystatin-related prostate protein (Cstrp) map to chromosome 3q41. (1995) (8)
Identification of a new frameshift mutation and a duplication polymorphism in the CFTR gene in the Algerian population. (1992) (7)
A genetic polymorphism in a functional domain of human pregnancy zone protein: the bait region (1990) (7)
JAK 2 rearrangements , including the novel SEC 31 AJAK 2 fusion , are recurrent in classical Hodgkin lymphoma * (2011) (7)
Generation and Characterization of an Nxf7 Knockout Mouse to Study NXF5 Deficiency in a Patient with Intellectual Disability (2013) (7)
Nxf7 deficiency impairs social exploration and spatio-cognitive abilities as well as hippocampal synaptic plasticity in mice (2015) (7)
Erratum: Gene prioritization through genomic data fusion (2006) (6)
DEFECTIVE RECEPTOR BINDING OF NATURALLY OCCURRING α2‐MACROGLOBULIN‐PROTEASE COMPLEXES IN CYSTIC FIBROSIS BY NORMAL HUMAN FIBROBLASTS a (1983) (6)
Report of the International Meeting on Chromosome 12 Genes in Cancer. (1996) (6)
Comparative expressed sequence hybridization studies of t(11;18)(q21;q21)-positive and -negative gastric MALT lymphomas reveal both unique and overlapping gene programs (2010) (6)
A physical map of the chromosome 12 centromere (2004) (6)
Design of a new protease inhibitor by the manipulation of the bait region of alpha 2-macroglobulin: inhibition of the tobacco etch virus protease by mutant alpha 2-macroglobulin. (1995) (6)
MONOCLONAL ANTIBODIES TOWARD THE RECEPTOR‐RECOGNITION SITE ON α2‐MACROGLOBULIN COMPLEXES a (1983) (6)
Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes. (1994) (5)
Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males (2006) (5)
Rapid and simple detection of minisatellite regions in forensic DNA samples by the polymerase chain reaction combined with a chemiluminescence method. (1990) (5)
Polymorphous endocytotic organelles in the receptor-mediated endocytosis of gold-labelled alpha 2-macroglobulin complexes by human fibroblasts. (1985) (5)
Assignment of the gene for the human proliferating cell nucleolar protein P120 (NOL1) to chromosome 12p13 by fluorescence in situ hybridization and polymerase chain reaction with somatic cell hybrids. (1994) (5)
A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene cluster on chromosome 13q32. (2001) (5)
Novel t(x;14)(p11.4;q32.33) resulting in upregulation of gpr34 and activation of the nfkb pathway is recurrent in malt lymphomas (2009) (5)
Submicroscopic deletions in 5 q-associated malignancies (2004) (5)
Three RFLPs associated with the human alpha 2-macroglobulin gene (A2M). (1985) (4)
An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptoms. (1992) (4)
Fusion of NUP214 to ABL1 on amplified extrachromosomal elements in T-ALL. (2004) (4)
Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive ALK tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesis (1999) (4)
A cluster of alpha 2-macroglobulin-related genes (alpha 2 M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an alpha 2M pseudogene. (1989) (4)
The gene for the peroxisomal targeting signal import receptor (PXR1) is located on human chromosome 12p13, flanked by TPI1 and D12S1089. (1995) (4)
Identification of intellectual disability genes in female patients with skewed X-inactivation (2015) (4)
Thermodynamic stability of the ammonium ions of ethylenediamine and histamine in montmorillonite (1978) (4)
alpha 2-Macroglobulin-proteinase complexes in cystic fibrosis serum. Analysis by monoclonal antibodies and receptor-mediated endocytosis by normal human fibroblasts. (1984) (4)
DUSP4 expression level in colorectal primaries predicts overall survival benefit in Kras wild-type and Kras mutant colorectal cancer after treatment with cetuximab for metastatic disease (2008) (4)
FISH analysis of typical t(5;12) (q32;p12) and variant t(10;12)(q23;p12) translocation in four patients with chronic myeloid disorders (1994) (4)
Rapid nonradioactive detection of point mutations in codon 12, 13 and 61 of the N-ras gene (1990) (4)
High-speed automated detection of PCR-amplified VNTR alleles: application to the apolipoprotein B 3' hypervariable region (1993) (4)
Molecular characterization of a t(2;3)(p23;q26): A recurrent translocation involving the EVI1 gene (2001) (3)
Breakpoint analysis by fluorescence in situ hybridization in myelodysplastic syndromes with t(3;12)(q26;p13) and expression of EVI1 (2000) (3)
Characterization of the human alpha 2-macroglobulin gene promoter: identification of a novel, triple TRE/RARE/ERE response element. (1994) (3)
The t(11;18)(q21;q21) characterizes a subgroup of extranodal MALT lymphomas: a two-color fluor-escence in situ hybridization study using AP12 and MLT specific probes (1999) (3)
BIRC3 (baculoviral IAP repeat-containing 3) (2011) (3)
Synthesis of a Cys949Tyr alpha 2-macroglobulin thiol ester mutant: co-transfection with wild-type alpha 2-macroglobulin in an episomal expression system. (1995) (3)
Absence of specific binding of receptor-mediated endocytosis, and of secretion of alpha-2-macroglobulin by cultured endothelial cells. (1982) (3)
Fusion between the apoptosis inhibitor gene AP12 and a novel 18q gene MLT , rearranged in the t(11,18)(q21;q21), marks half of the gastro-intestinal MALT type lymphomas without large cell proliferation (1999) (3)
FOXP1, a highly expressed gene in a subset of DLBCL, is targeted by a recurrent t(3;14)(p13;q32) (2004) (3)
Proteolysis at a lysine residue abolishes the receptor-recognition site of alpha 2-macroglobulin complexes. (1982) (3)
Chromosome mapping using polymerase chain reaction on somatic cell hybrids. (1990) (3)
Competitive in situ hybridization in a mediastinal germ cell tumor. (1994) (3)
lymphoblastic leukemia allele: two frequently associated alterations found in childhood acute The 12;21 translocation involving TEL and deletion of the other TEL (2011) (3)
A novel t(4;9)(q21;p24) fuses SEC31A to JAK2 in nodular-sclerosis Hodgkin lymphoma (2008) (3)
The TET RNA-binding proteins, EWSR1 and TAF15, are involved in acute lymphoblastic leukemia, through fusion with a new transcription factor, CIZ/NMP4 (2002) (2)
Association between XV2c/CS7/KM19/D9 haplotypes and the ΔF508 mutation A study of 57 Belgian families (1990) (2)
Oncogenic Properties of the T-ALL Associated EML1-ABL1 and NUP214-ABL1 Fusion Proteins. (2006) (2)
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: frequent increased gene dosage of known XLMR genes (2007) (2)
SSCP: a tool for contig building of duplicated genomic regions (2000) (2)
Distribution of HLA Class II Genes in a Caucasian Population as Determined by PCR and Reversed-Dot-Blot Typing (1994) (2)
In vitro validation of gamma-secretase inhibitors for the treatment of T-cell acute lymphoblastic leukemia (2007) (2)
The der(12)t(12;16) breakpoint in an acute leukaemia case targets a Sec7 domain containing protein. (2005) (2)
Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescents. (1993) (2)
EML1-ABL1 is activated by coiled coil mediated oligomerization and induces T-cell acute lymphoblastic or chronic myeloid leukemia in a mouse bone marrow transplant model (2007) (2)
Molecular karkyotyping detecs structural low grade mosaics in 4 % of patietns with idiopathic mental retardation and multiple congenital aberrations (2005) (2)
Characterization of the genes rearranged in the t(11;18) (q21; q21) associated with MALT lymphomas (1999) (2)
563 POSTER In vitro activity of the multi-targeted kinase inhibitor sorafenib (BAY43-9006) against gastrointestinal stromal tumor (GIST) mutants refractory to imatinib mesylate (2006) (2)
The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability (2013) (2)
Monoclonal antibodies toward the receptor-recognition site on alpha 2-macroglobulin complexes. (1983) (1)
TO JMG Mild Wolf-Hirschhorn syndrome : microarray CGH analysis of atypical 4 p 16 . 3 deletions enables refinement of the genotype-phenotype map (2004) (1)
Identification and characterisation of BTL, a new fusion partner of ETV6 in 1 T-ALL case and 2 AML cases with a translocation t(4;12) (q11;p13) (1998) (1)
Activity of dasatinib (BMS-354826), a dual SRC/ABL kinase inhibitor, and IPI-504, a heat shock protein 90 inhibitor, against thet imatinib-resistant PDGFRαD842V catalytic domain mutation in gastrointestinal stromal tumors (2008) (1)
ArrayCGH mapping of the chromosome 14q deletions in CLL (2006) (1)
Novel class II HLA-DRB4 and DPB1 alleles found in the Belgian population (2004) (1)
Molecular cytogenetic characterization of the chromosome 11 and 18 breakpoints in the t(11;18)(q21;q21) associated with malt lymphomas (1998) (1)
AP12-MLT transgenic mice: A model for the pathogenesis of MALT lymphomas? (2003) (1)
Involvement of the Notch1 and Notch2 genes in B-cell lymphomagen (2006) (1)
Identification of a new leukemia/lymphoma-associated breakpoint cluster involving PDL1 and PDL2 (2009) (1)
Telomere length regulation in telomerase positive murine cell line (1998) (1)
Partial hemizygous deletion of ETV6 gene in two AML cases with an add(12)(p13) (1996) (1)
Aberrations of the 9p24 region harboring JAK2, PDL1 and PDL2 genes are recurrent in classical hodgkin lymphoma (2010) (1)
Duplication and rearrangement of the MYB oncogene in T-cellacute lymphoblastic leukemia (2007) (1)
Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1. (1999) (1)
Cryptic 9p24 microdeletions covering hsa-mir-101-2 are recurrent in hematological malignancies (2009) (1)
P66: Identification of genes involved in T-cell oncogenesis through FISH screening of TCR rearrangements in T-ALL (2005) (1)
Micro-array CGH analysis of 4p microdeletions refines the genotype-phenotype map of the region and pinpoints low copy repeats as susceptibility sites for terminal chromosomal deletions (2004) (1)
JAK2 is targeted by recurrent translocations in classical Hodgkin lymphoma (2010) (1)
Ubiquitin Chains B by Cleaving Malt 1 κ Signaling to NFA 20 Negatively Regulates T Cell Receptor (2009) (1)
MALT1 (mucosa associated lymphoid tissue lymphoma translocation gene 1) (2011) (1)
Gene prioritization by genomic data fusion (2007) (1)
FIP1L1-PDGFRα D842V, a Novel Panresistant Mutant, Emerges after Treatment of FIP1L1-PDGFRα T674I Eosinophilic Leukemia with Single Agent Sorafenib (2008) (1)
Temperature‐Dependent Biosynthesis of Thiol Esters in Baculovirus Recombinant α2M and PZP (1994) (1)
NOTCH1 Is Targeted by Ig Translocations in NHL. (2005) (1)
TEL rearrangements in a childhood acute leukemias associtated with A t(7;12)(p15;p13) (1995) (1)
Regional assignment of seven loci to 12p13.2-pter by PCR analysis of somatic cell hybrids containing the der(12) or the der(X) chromosome from a mesothelioma showing t(X;12)(q22;p13). (1994) (1)
Receptor‐mediated endocytosis of α2macroglobulin—protease complexes by fibroblasts in culture (2001) (1)
Array-CGH analysis of T-ALL patients and cell lines (2006) (1)
Further Characterization of the Human Peroxisomal C‐Terminal Targeting Signal Protein Import Receptor (1996) (1)
Instructions for the preparation of gene mapping reports (1995) (1)
Chromosomal rearrangements affecting ABL1 in T-cell acute lymphoblastic (2004) (1)
Human osteosarcoma derived clonal variants: stable differences in cell surface composition. (1982) (1)
Cryptic rearrangements of the ALK gene in ALK-expressing diffuse large B-cell lymphoma (2008) (1)
Synthesis of a Cys949Tyr 2-macroglobulin thiol ester mutant: co-transfection with wild-type x2-macroglobulin in an episomal expression system (2005) (1)
Tyrosine kinases as possible therapeutic targets in chordoma (2009) (1)
Rat hemoglobin interferes with DNA migration in agarose gels. (1988) (1)
Distinct oncogenic properties of NUP214-ABL1 in T-cell acute lymphoblastic leukemia (2005) (1)
Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male (1999) (1)
Interstitial del(14)(Q) involving IGH are recurrent in MM (2007) (1)
Sorafenib (BAY43-9006) is a potent inhibitor of FIP1L1-PDGFR α and the imatinib resistant FIP1L1-PDGFR α T674I mutant (2006) (1)
Functional characterization of the T-ALL associated EML1-ABL1 and NUP214-ABL1 oncogenes (2007) (1)
P. Meera Khan (1998) (1)
Clinical characteristics of hypereosinophilic syndromes with an interstitial 4q12 deletion resulting in a FIP1L1-PDGFRA fusion gene (2003) (1)
Correction: Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability (2014) (0)
myelodysplastic syndromes in recurring chromosomal abnormality involving the TEL gene (ETV6) Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a (2011) (0)
Subject Index, Vol. 72, 1996 (1996) (0)
Detection of the t(11;18)(q21;q21) on frozen and paraffin-embedded tissue using interphase FISH with API2 and MLT specific probes (2000) (0)
Subject Index, Vol. 68, 1995 (1995) (0)
DNA-Amplification of Hypervariable Regions and HLA-Sequences as a Tool in Paternity Determinations and Forensic Medicine (1990) (0)
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation (2014) (0)
Identification of new genes and genetic mechanisms in patients with X-linked mental retardation (2006) (0)
ArrayCGH analysis detects cryptic chromosomal aberrations in more than twenty percent of patients with idiopathic mental retardation and multiple congenital anomalies (2005) (0)
Hypereosinophilic SyndromeResearch Paper (2005) (0)
Jak2 is a candidate target of genomic amplification in hematological malignancies (2003) (0)
Myeloid cell diff erentiation arrest by miR-125b-1 in myelodysplasic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation Most chromosomal translocations in myelodysplastic syndromes (MDS) (2008) (0)
Development and Exploitation of a Human Chromosomal Vector (2007) (0)
Alternative mechanisms for the involvement of ETV6 in hematological disorders (1998) (0)
Contents Vol. 68, 1999 (1999) (0)
Subject Index Vol. 85, 1999 (1999) (0)
A new subtype of pre-B-ALL with t(5;12)(q31q33;p12), molecularly and cytogenetically distinct from t(5;12) in CMML (1996) (0)
Temperature-dependent biosynthesis of thiol esters in baculovirus recombinant alpha 2M and PZP. (1994) (0)
A new autosomal dominant syndrome with multiple café-au-lait spots, freckling and macrocrania (2008) (0)
Identification ofInternal Variation inthePseudoautosomal VNTR DXYS17,withNonrandomDistribution ofthe Alleles on theX andtheY Chromosomes (1994) (0)
Screening of submicroscopic genomic aberrations in patients with X-linked mental retardation by high resolution array-CGH (2005) (0)
Transforming properties of the brain-specific homeobox gene GSH2 and ectopic expression in acute myeloid leukemias with a t(4;12)(q11;p13) involving the ETV6 gene (2000) (0)
Characterization of Notl end clones mapping to human chromosome 12p. (1991) (0)
Juxtamembrane Domain Truncation Is Sufficient for Activation of the FIP1L1-PDGFRα and ETV6-PDGFRβ Fusion Kinases. (2005) (0)
Genotype-phenotype correlation by fish and microarray cgh in atypical Wolf-Hirschhorn patients (2004) (0)
Linkage analysis in nonspecific X-linked mental retardation (1995) (0)
Strategies for targeted therapy of NUP214-ABL1 positive T-cell acute lymphoblastic leukemias (2006) (0)
Different chromosome translocations involve TEL gene in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) (1996) (0)
Contents Vol. 85, 1999 (1999) (0)
DNA methylation profiling in patients with mental retardation by chip-on-chip (2008) (0)
Contents, Vol. 11, 1982 (1982) (0)
The long-chain fatty acid-coa ligase 4 (FACL4) gene is mutated in family MRX68 (2004) (0)
architecture-driven DNA breaks and break-induced replication duplications mediated by genomicMECP 2 Nonrecurrent Material Supplemental (2008) (0)
t(11;18)(q21;q21) (2011) (0)
O3: Array CGH findings in a large series of 150 patients with idiopathic mental retardation and congenital anomalies: unexpected findings and implications for future routine diagnostic screening (2005) (0)
A full coverage high-resolution X-chromosome array for the detection of submicroscopic genomic copy number changes in patients with mental retardation (2005) (0)
ATIC, an enzyme involved in purine nucleotide biosynthesis anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive (2013) (0)
Whole genome sequencing in patients with the Hallermann-Streiff syndrome (2011) (0)
Genomics of MECP2 duplications (2008) (0)
The thermodynamic stability of the mono- and biprotonated ethylenediamine and histamine in montmorillonite (1977) (0)
O5: Characterization of subtle copy number changes on the X chromosome identified in 7% of patients with X-linked mental retardation by high-resolution array-CGH (2005) (0)
Properties of the NUP214-ABL1 fusion protein and consequences for treatment of T-cell acute lymphoblastic leukemia (2006) (0)
O4: Detection of structural low-grade mosaicism by array CGH (2005) (0)
Isolation and Characterisation of NotI-end Cosmids Mapping to Human Chromosome 12p (1994) (0)
Sorafenib Potently Inhibits ETV6-PDGFRβ and FLT3 Mutants, and Shows Activity Against FLT3 Mutants That Are Resistant to Other Small Molecule Inhibitors. (2006) (0)
Breakpoint cloning of aberrations on the X chromosome: identification of an unusual type of recombination that results in a dosage-dependent severity of the phenotype (2010) (0)
Functional characterization of the T-cell acute lymphoblastic leukemia (T-ALL) associated EML1-ABL1 and NUP214-ABL1 oncogenes (2007) (0)
B-cell lymphoma ALK activation by the CLTC-ALK fusion is a recurrent event in large (2013) (0)
Duplications of the MECP2 region are commonly found in a specific subset of MR patients; towards a detailed genotype-phenotype correlation (2006) (0)
In-vitro activity of the multi-targeted receptor tyrosine kinase inhibitor sunitinib malate (SU11248) against gastrointestinal stromal tumor (GIST) mutants refractory to imatinib mesylate (2005) (0)
Acute Lymphoblastic LeukemiaMolecular Basis of Disease (2005) (0)
ArrayCGH detects mosaics in similar to 4% of patients with MR/CA (2005) (0)
positive chronic eosinophilic leukemia - The EOL-1 cell line as an in vitro model for the study of FIP1L1-PDGFRA (2013) (0)
This information is current as Ubiquitin Chains B by Cleaving Malt 1 κ Signaling to NFA 20 Negatively Regulates T Cell Receptor (2009) (0)
Cancer and differentiation: The function of ATOH1 in cancer (2006) (0)
A microdeletion of the X chromosome is the probable cause of non-specific mental retardation in a Belgian family (1995) (0)
Transforming properties of TEL/JAK2 fusion proteins in hematopoietic cells. (1997) (0)
Translocation t(1;6): a recurrent TRANSLOCATION in B-cell CLL (2003) (0)
Study of telomere length regulation in human-mouse hybrid cell lines (2000) (0)
Contents Vol. 123, 2008 (2009) (0)
Mammalian peroxisomal acyl-CoA oxidases. III. Molecular cloning and further characterization of human branched chain acyl-CoA oxidase (1996) (0)
Use of a chromosomal vector for the study of gene dosage effects in mice and functional elements that underpin chromosome stability (2007) (0)
Chromosome 12p rearrangements in myeloid disorders: FISH investigation of 74 cases and molecular cloning of t(4;12)(q21;p13) in AML (1999) (0)
Telomere lengthening in a human mouse hybrid cell line: FISH and CSLM as a tool to measure telomere length of individual chromosomes (1999) (0)
TEL-AML1 gene fusion, deletion of TEL and rearrangement of KIP1 in a case of childhood ALL with a dic(12;13)(p11;q10) and other chromosomal anomalies (1996) (0)
The RAB-binding protein synaptotagmin-like 5 (SYTL5), interrupted in an MR patient, is not involved in the MR phenotype (2004) (0)
Rearrangement between MYH11 gene at 16p13 and a gene within cosmid D12S158 at 12p13.3 in a case of AML-M1 with bone marrow eosinophilia (1997) (0)
Chronic Myelogenous Leukemia Complex variant Philadelphia translocations involving the short arm of chromosome 6 in chronic myeloid leukemia (2002) (0)
Complex genomic architecture at xq28 results in duplication of mecp2 commonly found in a specific subset of MR patients (2007) (0)
The genetic profile of marginal zone B-cell lymphoma (1999) (0)
Duplications of the MECP2 gene are commonly found in a specific subset of patients with syndromal MR; towards a detailed genotype-phenotype correlation (2006) (0)
European Mathematical Genetics Meeting, Heidelberg, Germany, 12th–13th April 2007 (2007) (0)
Mental retardation-related gene duplications: more common than expected? (2006) (0)
Subject Index, Vol. 11, 1982 (1982) (0)
Consistent amplification of JAK2 in hematological malignancies with HSR(9)(P) (2000) (0)
Absence of specific binding, endocytosis and production of a2M by endothelial cells (1981) (0)
MHH-TALL1, a T-ALL Cell Line Expressing a Novel BCR-ABL Transcript. (2004) (0)
Genetic background-specific processing of artificial (sub)telomeres on a linearized chromosomal vector in telomerase-positive mammalian and avian cells (2007) (0)
Telomere length regulation and telomerase regulation in a telomerase positive human-murine hybrid cell line (1998) (0)
Construction and validation of array-cgh for the detection of microdeletions and –duplications in mr patients (2004) (0)
Analyses of chromosomal abnormalities involving the MLT/MALT1 gene in marginal zone B-cell lymphoma using a novel interphase FISH assay (2003) (0)
High resolution analysis by PCR on an automated DNA sequencer of internal variation at a pseudoautosomal VNTR (DXYS17) (1994) (0)
PDGFRA mutation in a family with intestinal neurofibromatosis: Relation with familial GIST (2006) (0)
1q duplication evidenced by chromosome microdissection in a case of marginal-zone B-cell lymphoma (1997) (0)
Rathemoglobin interferes withDNA migration inagarose gels (1988) (0)
The male face of MECP2: double gene dosage leads to a specific MR phenotype: towards a detailed genotype-phenotype correlation (2006) (0)
130 Polysomy for a 20q- chromosome masked by multiple markers in a case of secondary MDS (1997) (0)
New rearrangements of ETV6 supporting its dual involvement in the development of hematologic malginancies (1996) (0)
A Neo-Antigen Present on Complex α2M, Related to the Receptor Recognition Site (1982) (0)
A new genetic subset of acute lymphoblastic leukemia in both children and adults is identified by the t(12;17)(p13;q11) and its variant t(12;22)(p13;q12) (2002) (0)

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