Rouillac C - Search Results

1

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

2

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

3

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

4

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.

5

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

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

Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypes.

Rouillac C, Gane P, Cartron J, Le Pennec PY, Cartron JP, Colin Y. Rouillac C, et al. Blood. 1996 Jun 1;87(11):4853-61. Blood. 1996. PMID: 8639859 Free article.

8

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

9

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

10

Rearrangements of the blood group RhD gene associated with the DVI category phenotype.

Mouro I, Le Van Kim C, Rouillac C, van Rhenen DJ, Le Pennec PY, Bailly P, Cartron JP, Colin Y. Mouro I, et al. Among authors: rouillac c. Blood. 1994 Feb 15;83(4):1129-35. Blood. 1994. PMID: 8111052 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

14 results

Search Page

Filters