Meunier-Rotival M - Search Results

1

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: meunier rotival m. J Pediatr Gastroenterol Nutr. 2007 Apr;44(4):453-8. doi: 10.1097/MPG.0b013e318036a569. J Pediatr Gastroenterol Nutr. 2007. PMID: 17414143

2

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. Gastroenterology. 1999 May;116(5):1141-8. doi: 10.1016/s0016-5085(99)70017-x. Gastroenterology. 1999. PMID: 10220506

3

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: meunier rotival 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

4

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: meunier rotival 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

5

Alagille syndrome. The widening spectrum of arteriohepatic dysplasia.

Crosnier C, Lykavieris P, Meunier-Rotival M, Hadchouel M. Crosnier C, et al. Among authors: meunier rotival 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.

6

Construction of a 3.7-Mb physical map within human chromosome 20p12 ordering 18 markers in the Alagille syndrome locus.

Pollet N, Dhorne-Pollet S, Deleuze JF, Boccaccio C, Driancourt C, Raynaud N, Le Paslier D, Hadchouel M, Meunier-Rotival M. Pollet N, et al. Genomics. 1995 Jun 10;27(3):467-74. doi: 10.1006/geno.1995.1078. Genomics. 1995. PMID: 7558028

7

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. Genomics. 1997 Jun 15;42(3):489-98. doi: 10.1006/geno.1997.4676. Genomics. 1997. PMID: 9205123

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: meunier rotival 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

Bleeding tendency in children with Alagille syndrome.

Lykavieris P, Crosnier C, Trichet C, Meunier-Rotival M, Hadchouel M. Lykavieris P, et al. Among authors: meunier rotival m. Pediatrics. 2003 Jan;111(1):167-70. doi: 10.1542/peds.111.1.167. Pediatrics. 2003. PMID: 12509572

10

[Molecular and clinical characteristics of a family with Alagille syndrome].

Cosme A, Cobo AM, Meunier-Rotival M, Hadchouel M, Jara P, Ojeda E, Bujanda L, Orbegozo J. Cosme A, et al. Among authors: meunier rotival m. Med Clin (Barc). 2008 Jan 19;130(1):17-9. doi: 10.1157/13114539. Med Clin (Barc). 2008. PMID: 18221641 Spanish.

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