Hadchouel M - Search Results

1

Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome.

Crosnier C, Driancourt C, Raynaud N, Dhorne-Pollet S, Pollet N, Bernard O, Hadchouel M, Meunier-Rotival M. Crosnier C, et al. Among authors: hadchouel m. Gastroenterology. 1999 May;116(5):1141-8. doi: 10.1016/s0016-5085(99)70017-x. Gastroenterology. 1999. PMID: 10220506

2

Expression of mutant JAGGED1 alleles in patients with Alagille syndrome.

Boyer J, Crosnier C, Driancourt C, Raynaud N, Gonzales M, Hadchouel M, Meunier-Rotival M. Boyer J, et al. Among authors: hadchouel m. Hum Genet. 2005 May;116(6):445-53. doi: 10.1007/s00439-005-1262-7. Epub 2005 Mar 17. Hum Genet. 2005. PMID: 15772854

3

Biological function of mutant forms of JAGGED1 proteins in Alagille syndrome: inhibitory effect on Notch signaling.

Boyer-Di Ponio J, Wright-Crosnier C, Groyer-Picard MT, Driancourt C, Beau I, Hadchouel M, Meunier-Rotival M. Boyer-Di Ponio J, et al. Among authors: hadchouel m. Hum Mol Genet. 2007 Nov 15;16(22):2683-92. doi: 10.1093/hmg/ddm222. Epub 2007 Aug 24. Hum Mol Genet. 2007. PMID: 17720887

4

[Alagille syndrome in 1995. Clinical and genetic data].

Deleuze JF, Dhorne-Pollet S, Pollet N, Meunier-Rotival M, Hadchouel M. Deleuze JF, et al. Among authors: hadchouel m. Gastroenterol Clin Biol. 1995 Jun-Jul;19(6-7):587-96. Gastroenterol Clin Biol. 1995. PMID: 7590024 Review. French. No abstract available.

5

Segregation analysis of Alagille syndrome.

Dhorne-Pollet S, Deleuze JF, Hadchouel M, Bonaïti-Pellié C. Dhorne-Pollet S, et al. Among authors: hadchouel m. J Med Genet. 1994 Jun;31(6):453-7. doi: 10.1136/jmg.31.6.453. J Med Genet. 1994. PMID: 8071971 Free PMC article.

6

Construction of an integrated physical and gene map of human chromosome 20p12 providing candidate genes for Alagille syndrome.

Pollet N, Boccaccio C, Dhorne-Pollet S, Driancourt C, Raynaud N, Auffray C, Hadchouel M, Meunier-Rotival M. Pollet N, et al. Among authors: hadchouel m. Genomics. 1997 Jun 15;42(3):489-98. doi: 10.1006/geno.1997.4676. Genomics. 1997. PMID: 9205123

7

JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome.

Crosnier C, Attié-Bitach T, Encha-Razavi F, Audollent S, Soudy F, Hadchouel M, Meunier-Rotival M, Vekemans M. Crosnier C, et al. Among authors: hadchouel m. Hepatology. 2000 Sep;32(3):574-81. doi: 10.1053/jhep.2000.16600. Hepatology. 2000. PMID: 10960452

8

Fifteen novel mutations in the JAGGED1 gene of patients with Alagille syndrome.

Crosnier C, Driancourt C, Raynaud N, Hadchouel M, Meunier-Rotival M. Crosnier C, et al. Among authors: hadchouel m. Hum Mutat. 2001;17(1):72-3. doi: 10.1002/1098-1004(2001)17:1<72::AID-HUMU11>3.0.CO;2-U. Hum Mutat. 2001. PMID: 11139247

9

Alagille syndrome. The widening spectrum of arteriohepatic dysplasia.

Crosnier C, Lykavieris P, Meunier-Rotival M, Hadchouel M. Crosnier C, et al. Among authors: hadchouel m. Clin Liver Dis. 2000 Nov;4(4):765-78. doi: 10.1016/s1089-3261(05)70140-9. Clin Liver Dis. 2000. PMID: 11232356 Review.

10

Prenatal molecular diagnosis of inherited cholestatic diseases.

Jung C, Driancourt C, Baussan C, Zater M, Hadchouel M, Meunier-Rotival M, Guiochon-Mantel A, Jacquemin E. Jung C, et al. Among authors: hadchouel m. J Pediatr Gastroenterol Nutr. 2007 Apr;44(4):453-8. doi: 10.1097/MPG.0b013e318036a569. J Pediatr Gastroenterol Nutr. 2007. PMID: 17414143

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