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Wim Van de Ven

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Lieselot De Vos; Jeroen Declercq; Georgina Galicia Rosas; Boudewijn Van Damme; Anton J M Roebroek; Fons Vermorken; Jan Ceuppens; Wim Van de Ven; John W M Creemers
MMTV-cre-mediated fur inactivation concomitant with PLAG1 proto-oncogene activation delays salivary gland tumorigenesis in mice.
Isabelle Cleynen; Christel Huysmans; Takehiko Sasazuki; Senji Shirasawa; Wim Van de Ven; Kristel Peeters
Transcriptional control of the human high mobility group A1 gene: basal and oncogenic Ras-regulated expression.
Philippe Debeer; Hilde Van Esch; Christel Huysmans; E Pijkels; Luc De Smet; Wim Van de Ven; koenraad devriendt; Jean-Pierre Fryns
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).

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2008: Lieselot De Vos; Jeroen Declercq; Georgina Galicia Rosas; Boudewijn Van Damme; Anton J M Roebroek; Fons Vermorken; Jan Ceuppens; Wim Van de Ven; John W M Creemers
MMTV-cre-mediated fur inactivation concomitant with PLAG1 proto-oncogene activation delays salivary gland tumorigenesis in mice.
International journal of oncology 2008;32(5):1073-83.
2007: Isabelle Cleynen; Christel Huysmans; Takehiko Sasazuki; Senji Shirasawa; Wim Van de Ven; Kristel Peeters
Transcriptional control of the human high mobility group A1 gene: basal and oncogenic Ras-regulated expression.
Cancer research 2007;67(10):4620-9.
2005: Philippe Debeer; Hilde Van Esch; Christel Huysmans; E Pijkels; Luc De Smet; Wim Van de Ven; koenraad devriendt; Jean-Pierre Fryns
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).
European journal of medical genetics 2005;48(4):377-87.
2004: Dries Castermans; Valérie Wilquet; Jean Steyaert; Wim Van de Ven; Jean-Pierre Fryns; koenraad devriendt
Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.
Autism : the international journal of research and practice 2004;8(2):141-61.
2003: Dries Castermans; Valérie Wilquet; E Parthoens; Christel Huysmans; J Steyaert; L Swinnen; Jean-Pierre Fryns; Wim Van de Ven; koenraad devriendt
The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.
Journal of medical genetics 2003;40(5):352-6.
2003: Hilde Peeters; Philippe Debeer; Amos Bairoch; Valérie Wilquet; Christel Huysmans; E Parthoens; Jean-Pierre Fryns; Marc Gewillig; Y Nakamura; N Niikawa; Wim Van de Ven; koenraad devriendt
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse.
Human genetics 2003;112(5-6):573-80.
2001: Hilde Peeters; Philippe Debeer; Peter Groenen; Hilde Van Esch; G Vanderlinden; Benedicte Eyskens; Luc Mertens; Marc Gewillig; Wim Van de Ven; Jean-Pierre Fryns; koenraad devriendt
Recurrent involvement of chromosomal region 6q21 in heterotaxy.
American journal of medical genetics 2001;103(1):44-7.
2000: Hilde Van Esch; Peter Groenen; M Andrew Nesbit; S Schuffenhauer; Peter Lichtner; G Vanderlinden; Brian Harding; R Beetz; R W Bilous; I Holdaway; N J Shaw; Jean-Pierre Fryns; Wim Van de Ven; Rajesh V Thakker; koenraad devriendt
GATA3 haplo-insufficiency causes human HDR syndrome.
Nature 2000;406(6794):419-22.
1999: Hilde Van Esch; Peter Groenen; S Daw; A Poffyn; Maureen Holvoet; P Scambler; Jean-Pierre Fryns; Wim Van de Ven; koenraad devriendt
Partial DiGeorge syndrome in two patients with a 10p rearrangement.
Clinical genetics 1999;55(4):269-76.
1999: Hilde Van Esch; Peter Groenen; Jean-Pierre Fryns; Wim Van de Ven; koenraad devriendt
The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.
Genetic counseling (Geneva, Switzerland) 1999;10(1):59-65.
1998: koenraad devriendt; Peter Groenen; Hilde Van Esch; M van Dijck; Wim Van de Ven; Jean-Pierre Fryns; W Proesmans
Vesico-ureteral reflux: a genetic condition?
European journal of pediatrics 1998;157(4):265-71.
1997: L Van Rompaey; Torik A Y Ayoubi; Wim Van de Ven; Peter Marynen
Inhibition of intracellular proteolytic processing of soluble proproteins by an engineered alpha 2-macroglobulin containing a furin recognition sequence in the bait region.
The Biochemical journal 1997;326 ( Pt 2)():507-14.
1996: Juan Rosai; Måns Akerman; Paola Dal Cin; I DeWever; Christopher D M Fletcher; Nils Mandahl; Fredrik Mertens; Felix Mitelman; Anders Rydholm; Raf Sciot; Giovanni Tallini; Herman Van Den Berghe; Wim Van de Ven; Roberta Vanni; H Willen
Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group).
The American journal of surgical pathology 1996;20(10):1182-9.
1996: Nils Mandahl; Måns Akerman; Pierre Aman; Paola Dal Cin; Ivo De Wever; Christopher D M Fletcher; Fredrik Mertens; Felix Mitelman; Juan Rosai; Anders Rydholm; Raf Sciot; Giovanni Tallini; Herman Van Den Berghe; Wim Van de Ven; Roberta Vanni; Helena Willén
Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors: a report of the CHAMP collaborative study group. CHromosomes And MorPhology.
International journal of cancer. Journal international du cancer 1996;67(5):632-5.
1996: Christopher D M Fletcher; Måns Akerman; Paola Dal Cin; Ivo De Wever; Nils Mandahl; Fredrik Mertens; Felix Mitelman; Juan Rosai; Anders Rydholm; Raf Sciot; Giovanni Tallini; Herman Van Den Berghe; Wim Van de Ven; Roberta Vanni; H Willen
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
The American journal of pathology 1996;148(2):623-30.
1995: Paola Dal Cin; Roberta Vanni; S Marras; Philippe Moerman; P Kools; M Andria; E Valdes; J Deprest; Wim Van de Ven; Herman Van Den Berghe
Four cytogenetic subgroups can be identified in endometrial polyps.
Cancer research 1995;55(7):1565-8.
1993: Paola Dal Cin; P Kools; I De Jonge; Philippe Moerman; Wim Van de Ven; Herman Van Den Berghe
Rearrangement of 12q14-15 in pulmonary chondroid hamartoma.
Genes, chromosomes & cancer 1993;8(2):131-3.
1993: Paola Dal Cin; P Kools; Raf Sciot; Ivo De Wever; B Van Damme; Wim Van de Ven; Herman Van Den Berghe
Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors.
Cancer genetics and cytogenetics 1993;68(2):85-90.