Van De Ven WJ - Search Results

1

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.

Castermans D, Volders K, Crepel A, Backx L, De Vos R, Freson K, Meulemans S, Vermeesch JR, Schrander-Stumpel CT, De Rijk P, Del-Favero J, Van Geet C, Van De Ven WJ, Steyaert JG, Devriendt K, Creemers JW. Castermans D, et al. Among authors: de vos r, van de ven wj, de rijk p, van geet c. Hum Mol Genet. 2010 Apr 1;19(7):1368-78. doi: 10.1093/hmg/ddq013. Epub 2010 Jan 12. Hum Mol Genet. 2010. PMID: 20071347

2

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

Castermans D, Vermeesch JR, Fryns JP, Steyaert JG, Van de Ven WJ, Creemers JW, Devriendt K. Castermans D, et al. Among authors: van de ven wj. Eur J Hum Genet. 2007 Apr;15(4):422-31. doi: 10.1038/sj.ejhg.5201785. Epub 2007 Feb 7. Eur J Hum Genet. 2007. PMID: 17290275

3

Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autism.

Castermans D, Thienpont B, Volders K, Crepel A, Vermeesch JR, Schrander-Stumpel CT, Van de Ven WJ, Steyaert JG, Creemers JW, Devriendt K. Castermans D, et al. Among authors: van de ven wj. Eur J Hum Genet. 2008 Oct;16(10):1187-92. doi: 10.1038/ejhg.2008.71. Epub 2008 Apr 16. Eur J Hum Genet. 2008. PMID: 18414512

4

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

Castermans D, Wilquet V, Steyaert J, Van de Ven W, Fryns JP, Devriendt K. Castermans D, et al. Autism. 2004 Jun;8(2):141-61. doi: 10.1177/1362361304042719. Autism. 2004. PMID: 15165431 Review.

5

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse.

Peeters H, Debeer P, Bairoch A, Wilquet V, Huysmans C, Parthoens E, Fryns JP, Gewillig M, Nakamura Y, Niikawa N, Van de Ven W, Devriendt K. Peeters H, et al. Hum Genet. 2003 May;112(5-6):573-80. doi: 10.1007/s00439-003-0917-5. Epub 2003 Feb 27. Hum Genet. 2003. PMID: 12607115

6

Sesn1 is a novel gene for left-right asymmetry and mediating nodal signaling.

Peeters H, Voz ML, Verschueren K, De Cat B, Pendeville H, Thienpont B, Schellens A, Belmont JW, David G, Van De Ven WJ, Fryns JP, Gewillig M, Huylebroeck D, Peers B, Devriendt K. Peeters H, et al. Among authors: van de ven wj, de cat b. Hum Mol Genet. 2006 Nov 15;15(22):3369-77. doi: 10.1093/hmg/ddl413. Epub 2006 Oct 12. Hum Mol Genet. 2006. PMID: 17038485 Free article.

7

Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11).

Debeer P, Mols R, Huysmans C, Devriendt K, Van de Ven WJ, Fryns JP. Debeer P, et al. Among authors: van de ven wj. Clin Genet. 2002 Nov;62(5):410-4. doi: 10.1034/j.1399-0004.2002.620510.x. Clin Genet. 2002. PMID: 12431258

8

Recurrent involvement of chromosomal region 6q21 in heterotaxy.

Peeters H, Debeer P, Groenen P, Van Esch H, Vanderlinden G, Eyskens B, Mertens L, Gewillig M, Van de Ven W, Fryns JP, Devriendt K. Peeters H, et al. Am J Med Genet. 2001 Sep 15;103(1):44-7. doi: 10.1002/ajmg.1499. Am J Med Genet. 2001. PMID: 11562933

9

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.

Castermans D, Wilquet V, Parthoens E, Huysmans C, Steyaert J, Swinnen L, Fryns JP, Van de Ven W, Devriendt K. Castermans D, et al. J Med Genet. 2003 May;40(5):352-6. doi: 10.1136/jmg.40.5.352. J Med Genet. 2003. PMID: 12746398 Free PMC article. No abstract available.

10

Curbing activation: proprotein convertases in homeostasis and pathology.

Taylor NA, Van De Ven WJ, Creemers JW. Taylor NA, et al. Among authors: van de ven wj. FASEB J. 2003 Jul;17(10):1215-27. doi: 10.1096/fj.02-0831rev. FASEB J. 2003. PMID: 12832286 Review.

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