Baral V - Search Results

1

Endothelin-3 stimulates cell adhesion and cooperates with β1-integrins during enteric nervous system ontogenesis.

Gazquez E, Watanabe Y, Broders-Bondon F, Paul-Gilloteaux P, Heysch J, Baral V, Bondurand N, Dufour S. Gazquez E, et al. Among authors: baral v. Sci Rep. 2016 Dec 1;6:37877. doi: 10.1038/srep37877. Sci Rep. 2016. PMID: 27905407 Free PMC article.

2

Sox10 and Itgb1 interaction in enteric neural crest cell migration.

Watanabe Y, Broders-Bondon F, Baral V, Paul-Gilloteaux P, Pingault V, Dufour S, Bondurand N. Watanabe Y, et al. Among authors: baral v. Dev Biol. 2013 Jul 1;379(1):92-106. doi: 10.1016/j.ydbio.2013.04.013. Epub 2013 Apr 19. Dev Biol. 2013. PMID: 23608456 Free article.

3

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: baral v. 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.

4

Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2.

Watanabe Y, Stanchina L, Lecerf L, Gacem N, Conidi A, Baral V, Pingault V, Huylebroeck D, Bondurand N. Watanabe Y, et al. Among authors: baral v. Gastroenterology. 2017 Apr;152(5):1139-1150.e4. doi: 10.1053/j.gastro.2016.12.034. Epub 2017 Jan 5. Gastroenterology. 2017. PMID: 28063956

5

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: baral v. Hum Mutat. 2011 Dec;32(12):1436-49. doi: 10.1002/humu.21583. Epub 2011 Sep 19. Hum Mutat. 2011. PMID: 21898658 Free article.

6

Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations.

Chaoui A, Kavo A, Baral V, Watanabe Y, Lecerf L, Colley A, Mendoza-Londono R, Pingault V, Bondurand N. Chaoui A, et al. Among authors: baral v. Hum Mol Genet. 2015 Sep 1;24(17):4933-47. doi: 10.1093/hmg/ddv215. Epub 2015 Jun 9. Hum Mol Genet. 2015. PMID: 26060192

7

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: baral v. 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.

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. 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

An impairment of long distance SOX10 regulatory elements underlies isolated Hirschsprung disease.

Lecerf L, Kavo A, Ruiz-Ferrer M, Baral V, Watanabe Y, Chaoui A, Pingault V, Borrego S, Bondurand N. Lecerf L, et al. Among authors: baral v. Hum Mutat. 2014 Mar;35(3):303-7. doi: 10.1002/humu.22499. Epub 2014 Jan 8. Hum Mutat. 2014. PMID: 24357527

10

Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.

Pingault V, Bodereau V, Baral V, Marcos S, Watanabe Y, Chaoui A, Fouveaut C, Leroy C, Vérier-Mine O, Francannet C, Dupin-Deguine D, Archambeaud F, Kurtz FJ, Young J, Bertherat J, Marlin S, Goossens M, Hardelin JP, Dodé C, Bondurand N. Pingault V, et al. Among authors: baral v. Am J Hum Genet. 2013 May 2;92(5):707-24. doi: 10.1016/j.ajhg.2013.03.024. Am J Hum Genet. 2013. PMID: 23643381 Free PMC article.

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