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Marga Schepens

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Eric F P M Schoenmakers; Jens Bunt; Maria Debiec-Rychter; Lianne Hermers; Erik H L P G Huys; Bert Janssen; Monique Kersten; Gerard F M Merkx; Patrick Pauwels; Marga Schepens; Ad Geurts van Kessel
Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma.
K Medendorp; Jan J M van Groningen; Marga Schepens; Lilian A Vreede; José Thijssen; Eric F P M Schoenmakers; Wilhelmina H van den Hurk; Ad Geurts van Kessel; Roland P Kuiper
Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas.
Roland P Kuiper; Marga Schepens; José Thijssen; Eric F P M Schoenmakers; Ad Geurts van Kessel
Regulation of the MiTF/TFE bHLH-LZ transcription factors through restricted spatial expression and alternative splicing of functional domains.

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All Publications

2013: Eric F P M Schoenmakers; Jens Bunt; Maria Debiec-Rychter; Lianne Hermers; Erik H L P G Huys; Bert Janssen; Monique Kersten; Gerard F M Merkx; Patrick Pauwels; Marga Schepens; Ad Geurts van Kessel
Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma.
Genes, chromosomes & cancer 2013;52(1):11-23.
2007: K Medendorp; Jan J M van Groningen; Marga Schepens; Lilian A Vreede; José Thijssen; Eric F P M Schoenmakers; Wilhelmina H van den Hurk; Ad Geurts van Kessel; Roland P Kuiper
Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas.
Cytogenetic and genome research 2007;118(2-4):157-65.
2004: Roland P Kuiper; Marga Schepens; José Thijssen; Eric F P M Schoenmakers; Ad Geurts van Kessel
Regulation of the MiTF/TFE bHLH-LZ transcription factors through restricted spatial expression and alternative splicing of functional domains.
Nucleic acids research 2004;32(8):2315-22.
2003: Daniëlle Bodmer; Marga Schepens; Marc J Eleveld; Eric F P M Schoenmakers; Ad Geurts van Kessel
Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21).
Genes, chromosomes & cancer 2003;38(2):107-16.
2003: Roland P Kuiper; Marga Schepens; José Thijssen; Martien van Asseldonk; Eva van den Berg; Julia Bridge; Ed Schuuring; Eric F P M Schoenmakers; Ad Geurts van Kessel
Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitution.
Human molecular genetics 2003;12(14):1661-9.
2003: Imke M Veltman; Marga Schepens; Leendert H J Looijenga; Louise C Strong; Ad Geurts van Kessel
Germ cell tumours in neonates and infants: a distinct subgroup?
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2003;111(1):152-60; discussion 160.
2002: Imke M Veltman; Martien van Asseldonk; Marga Schepens; hans stoop; Leendert H J Looijenga; Cokkie H Wouters; Lutgarde Govaerts; Ron Suijkerbuijk; Ad Geurts van Kessel
A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat.
Cancer genetics and cytogenetics 2002;136(1):17-22.
2002: Diederik R H de Bruijn; Nuno R. dos Santos; Ellen Kater-Baats; José Thijssen; Lieke van den Berk; Jiska Stap; Matthé Balemans; Marga Schepens; Gerard F M Merkx; Ad Geurts van Kessel
The cancer-related protein SSX2 interacts with the human homologue of a Ras-like GTPase interactor, RAB3IP, and a novel nuclear protein, SSX2IP.
Genes, chromosomes & cancer 2002;34(3):285-98.
2000: Frans A Hol; Marga Schepens; Sylvia van Beersum; E Redolfi; M Affer; Paolo Vezzoni; Ben C J Hamel; Pamela S Karnes; Edwin C M Mariman; Ileana Zucchi
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes.
Genomics 2000;69(2):174-81.
2000: Martien van Asseldonk; Marga Schepens; Diederik R H de Bruijn; B Janssen; Gerard F M Merkx; Ad Geurts van Kessel
Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.
Genomics 2000;66(1):35-42.
2000: A Simons; Marga Schepens; Judith W M Jeuken; Sandra H E Sprenger; G van de Zande; Bodil Bjerkehagen; Anne Forus; VM Weibolt; I Molenaar; Eva van den Berg; Ola Myklebost; J Bridge; Ad Geurts van Kessel; Ron Suijkerbuijk
Frequent loss of 9p21 (p16(INK4A)) and other genomic imbalances in human malignant fibrous histiocytoma.
Cancer genetics and cytogenetics 2000;118(2):89-98.
1999: A Simons; Marga Schepens; Anne Forus; Linda H Godager; Martien van Asseldonk; Ola Myklebost; Ad Geurts van Kessel
A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis.
Genes, chromosomes & cancer 1999;26(2):115-24.
1997: Hans van Bokhoven; J Kissing; Marga Schepens; Sylvia van Beersum; A Simons; P Riegman; J A McMahon; A P McMahon; Han G Brunner
Assignment of WNT7B to human chromosome band 22q13 by in situ hybridization.
Cytogenetics and cell genetics 1997;77(3-4):288-9.
1996: A M Riesewijk; Marga Schepens; E M Mariman; Hans-Hilger Ropers; Vera Kalscheuer
The MAS proto-oncogene is not imprinted in humans.
Genomics 1996;35(2):380-2.
1996: A M Riesewijk; Marga Schepens; T R Welch; E M van den Berg-Loonen; E M Mariman; Hans-Hilger Ropers; Vera Kalscheuer
Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription.
Genomics 1996;31(2):158-66.
1993: Vera Kalscheuer; Edwin C M Mariman; Marga Schepens; H Rehder; Hans-Hilger Ropers
The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans.
Nature genetics 1993;5(1):74-8.