Driancourt C - Search Results

1

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. Among authors: driancourt c. Genomics. 1995 Jun 10;27(3):467-74. doi: 10.1006/geno.1995.1078. Genomics. 1995. PMID: 7558028

2

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

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: driancourt c. 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

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

5

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: driancourt c. 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

6

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: driancourt c. 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

7

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

8

A boost of BMP4 accelerates the commitment of human embryonic stem cells to the endothelial lineage.

Goldman O, Feraud O, Boyer-Di Ponio J, Driancourt C, Clay D, Le Bousse-Kerdiles MC, Bennaceur-Griscelli A, Uzan G. Goldman O, et al. Among authors: driancourt c. Stem Cells. 2009 Aug;27(8):1750-9. doi: 10.1002/stem.100. Stem Cells. 2009. PMID: 19544443

9

A Novel Molecular and Functional Stemness Signature Assessing Human Cord Blood-Derived Endothelial Progenitor Cell Immaturity.

Guillevic O, Ferratge S, Pascaud J, Driancourt C, Boyer-Di-Ponio J, Uzan G. Guillevic O, et al. Among authors: driancourt c. PLoS One. 2016 Apr 4;11(4):e0152993. doi: 10.1371/journal.pone.0152993. eCollection 2016. PLoS One. 2016. PMID: 27043207 Free PMC article.

10

Instruction of circulating endothelial progenitors in vitro towards specialized blood-brain barrier and arterial phenotypes.

Boyer-Di Ponio J, El-Ayoubi F, Glacial F, Ganeshamoorthy K, Driancourt C, Godet M, Perrière N, Guillevic O, Couraud PO, Uzan G. Boyer-Di Ponio J, et al. Among authors: driancourt c. PLoS One. 2014 Jan 2;9(1):e84179. doi: 10.1371/journal.pone.0084179. eCollection 2014. PLoS One. 2014. PMID: 24392113 Free PMC article.

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