Goossens M - Search Results

1

Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development.

Stanchina L, Baral V, Robert F, Pingault V, Lemort N, Pachnis V, Goossens M, Bondurand N. Stanchina L, et al. Among authors: goossens m. Dev Biol. 2006 Jul 1;295(1):232-49. doi: 10.1016/j.ydbio.2006.03.031. Epub 2006 Apr 3. Dev Biol. 2006. PMID: 16650841 Free article.

2

Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.

Bondurand N, Dastot-Le Moal F, Stanchina L, Collot N, Baral V, Marlin S, Attie-Bitach T, Giurgea I, Skopinski L, Reardon W, Toutain A, Sarda P, Echaieb A, Lackmy-Port-Lis M, Touraine R, Amiel J, Goossens M, Pingault V. Bondurand N, et al. Among authors: goossens m. Am J Hum Genet. 2007 Dec;81(6):1169-85. doi: 10.1086/522090. Epub 2007 Oct 22. Am J Hum Genet. 2007. PMID: 17999358 Free PMC article.

3

Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development.

Stanchina L, Van de Putte T, Goossens M, Huylebroeck D, Bondurand N. Stanchina L, et al. Among authors: goossens m. Dev Biol. 2010 May 15;341(2):416-28. doi: 10.1016/j.ydbio.2010.02.036. Epub 2010 Mar 4. Dev Biol. 2010. PMID: 20206619 Free article.

4

Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4.

Bondurand N, Fouquet V, Baral V, Lecerf L, Loundon N, Goossens M, Duriez B, Labrune P, Pingault V. Bondurand N, et al. Among authors: goossens m. Eur J Hum Genet. 2012 Sep;20(9):990-4. doi: 10.1038/ejhg.2012.29. Epub 2012 Feb 29. Eur J Hum Genet. 2012. PMID: 22378281 Free PMC article.

5

Expression of the SOX10 gene during human development.

Bondurand N, Kobetz A, Pingault V, Lemort N, Encha-Razavi F, Couly G, Goerich DE, Wegner M, Abitbol M, Goossens M. Bondurand N, et al. Among authors: goossens m. FEBS Lett. 1998 Aug 7;432(3):168-72. doi: 10.1016/s0014-5793(98)00843-6. FEBS Lett. 1998. PMID: 9720918 Free article.

6

Review and update of mutations causing Waardenburg syndrome.

Pingault V, Ente D, Dastot-Le Moal F, Goossens M, Marlin S, Bondurand N. Pingault V, et al. Among authors: goossens m. Hum Mutat. 2010 Apr;31(4):391-406. doi: 10.1002/humu.21211. Hum Mutat. 2010. PMID: 20127975 Free article. Review.

7

Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndrome.

Chaoui A, Watanabe Y, Touraine R, Baral V, Goossens M, Pingault V, Bondurand N. Chaoui A, et al. Among authors: goossens m. Hum Mutat. 2011 Dec;32(12):1436-49. doi: 10.1002/humu.21583. Epub 2011 Sep 19. Hum Mutat. 2011. PMID: 21898658 Free article.

8

Screening of MITF and SOX10 regulatory regions in Waardenburg syndrome type 2.

Baral V, Chaoui A, Watanabe Y, Goossens M, Attie-Bitach T, Marlin S, Pingault V, Bondurand N. Baral V, et al. Among authors: goossens m. PLoS One. 2012;7(7):e41927. doi: 10.1371/journal.pone.0041927. Epub 2012 Jul 27. PLoS One. 2012. PMID: 22848661 Free PMC article.

9

SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism.

Pingault V, Girard M, Bondurand N, Dorkins H, Van Maldergem L, Mowat D, Shimotake T, Verma I, Baumann C, Goossens M. Pingault V, et al. Among authors: goossens m. Hum Genet. 2002 Aug;111(2):198-206. doi: 10.1007/s00439-002-0765-8. Epub 2002 Jul 6. Hum Genet. 2002. PMID: 12189494

10

SOX10 mutations in patients with Waardenburg-Hirschsprung disease.

Pingault V, Bondurand N, Kuhlbrodt K, Goerich DE, Préhu MO, Puliti A, Herbarth B, Hermans-Borgmeyer I, Legius E, Matthijs G, Amiel J, Lyonnet S, Ceccherini I, Romeo G, Smith JC, Read AP, Wegner M, Goossens M. Pingault V, et al. Among authors: goossens m. Nat Genet. 1998 Feb;18(2):171-3. doi: 10.1038/ng0298-171. Nat Genet. 1998. PMID: 9462749

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