Rouillac C - Search Results

1

Mapping of a congenital microcoria locus to 13q31-q32.

Rouillac C, Roche O, Marchant D, Bachner L, Kobetz A, Toulemont PJ, Orssaud C, Urvoy M, Odent S, Le Marec B, Abitbol M, Dufier JL. Rouillac C, et al. Am J Hum Genet. 1998 May;62(5):1117-22. doi: 10.1086/301841. Am J Hum Genet. 1998. PMID: 9545411 Free PMC article.

2

First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complex.

Rouillac C, Aral B, Fouque F, Marchant D, Saudubray JM, Dumez Y, Lindsay G, Abitbol M, Dufier JL, Marsac C, Benelli C. Rouillac C, et al. Prenat Diagn. 1999 Dec;19(12):1160-4. doi: 10.1002/(sici)1097-0223(199912)19:12<1160::aid-pd712>3.0.co;2-2. Prenat Diagn. 1999. PMID: 10590436

3

Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis.

Nandrot E, Dufour EM, Provost AC, Péquignot MO, Bonnel S, Gogat K, Marchant D, Rouillac C, Sépulchre de Condé B, Bihoreau MT, Shaver C, Dufier JL, Marsac C, Lathrop M, Menasche M, Abitbol MM. Nandrot E, et al. Among authors: rouillac c. Neurobiol Dis. 2000 Dec;7(6 Pt B):586-99. doi: 10.1006/nbdi.2000.0328. Neurobiol Dis. 2000. PMID: 11114258

4

Spatial and temporal expression of the cystathionine beta-synthase gene during early human development.

Quéré I, Paul V, Rouillac C, Janbon C, London J, Demaille J, Kamoun P, Dufier JL, Abitbol M, Chassé JF. Quéré I, et al. Among authors: rouillac c. Biochem Biophys Res Commun. 1999 Jan 8;254(1):127-37. doi: 10.1006/bbrc.1998.9079. Biochem Biophys Res Commun. 1999. PMID: 9920745

5

Insulin-like 4 (INSL4) gene expression in human embryonic and trophoblastic tissues.

Laurent A, Rouillac C, Delezoide AL, Giovangrandi Y, Vekemans M, Bellet D, Abitbol M, Vidaud M. Laurent A, et al. Among authors: rouillac c. Mol Reprod Dev. 1998 Oct;51(2):123-9. doi: 10.1002/(SICI)1098-2795(199810)51:2<123::AID-MRD1>3.0.CO;2-S. Mol Reprod Dev. 1998. PMID: 9740319

6

Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes.

Rouillac C, Colin Y, Hughes-Jones NC, Beolet M, D'Ambrosio AM, Cartron JP, Le Van Kim C. Rouillac C, et al. Blood. 1995 May 15;85(10):2937-44. Blood. 1995. PMID: 7742554 Free article.

7

Leu110Pro substitution in the RhD polypeptide is responsible for the DVII category blood group phenotype.

Rouillac C, Le Van Kim C, Beolet M, Cartron JP, Colin Y. Rouillac C, et al. Am J Hematol. 1995 May;49(1):87-8. doi: 10.1002/ajh.2830490115. Am J Hematol. 1995. PMID: 7741145

8

Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region.

Chérif-Zahar B, Le Van Kim C, Rouillac C, Raynal V, Cartron JP, Colin Y. Chérif-Zahar B, et al. Among authors: rouillac c. Genomics. 1994 Jan 1;19(1):68-74. doi: 10.1006/geno.1994.1014. Genomics. 1994. PMID: 8188244

9

Tentative model for the mapping of D epitopes on the RhD polypeptide.

Cartron JP, Rouillac C, Le Van Kim C, Mouro I, Colin Y. Cartron JP, et al. Among authors: rouillac c. Transfus Clin Biol. 1996;3(6):497-503. doi: 10.1016/s1246-7820(96)80070-x. Transfus Clin Biol. 1996. PMID: 9018815

10

The two-gene model of the RH blood-group locus.

Cartron JP, Le Van Kim C, Cherif-Zahar B, Mouro I, Rouillac C, Colin Y. Cartron JP, et al. Among authors: rouillac c. Biochem J. 1995 Mar 15;306 ( Pt 3)(Pt 3):877-8. doi: 10.1042/bj3060877. Biochem J. 1995. PMID: 7702587 Free PMC article. No abstract available.

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