Scoul C - Search Results

1

Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.

Küry S, Buecher B, Robiou-du-Pont S, Scoul C, Colman H, Le Neel T, Le Houérou C, Faroux R, Ollivry J, Lafraise B, Chupin LD, Sébille V, Bézieau S. Küry S, et al. Among authors: scoul c. BMC Cancer. 2008 Nov 7;8:326. doi: 10.1186/1471-2407-8-326. BMC Cancer. 2008. PMID: 18992148 Free PMC article.

2

Combinations of cytochrome P450 gene polymorphisms enhancing the risk for sporadic colorectal cancer related to red meat consumption.

Küry S, Buecher B, Robiou-du-Pont S, Scoul C, Sébille V, Colman H, Le Houérou C, Le Neel T, Bourdon J, Faroux R, Ollivry J, Lafraise B, Chupin LD, Bézieau S. Küry S, et al. Among authors: scoul c. Cancer Epidemiol Biomarkers Prev. 2007 Jul;16(7):1460-7. doi: 10.1158/1055-9965.EPI-07-0236. Cancer Epidemiol Biomarkers Prev. 2007. PMID: 17627011

3

The thorough screening of the MUTYH gene in a large French cohort of sporadic colorectal cancers.

Küry S, Buecher B, Robiou-du-Pont S, Scoul C, Colman H, Lelièvre B, Olschwang S, Le Houérou C, Le Neel T, Faroux R, Ollivry J, Lafraise B, Chupin LD, Bézieau S. Küry S, et al. Among authors: scoul c. Genet Test. 2007 Winter;11(4):373-9. doi: 10.1089/gte.2007.0029. Genet Test. 2007. PMID: 17931073

4

Molecular cloning and characterization of FBXO47, a novel gene containing an F-box domain, located in the 17q12 band deleted in papillary renal cell carcinoma.

Simon-Kayser B, Scoul C, Renaudin K, Jezequel P, Bouchot O, Rigaud J, Bezieau S. Simon-Kayser B, et al. Among authors: scoul c. Genes Chromosomes Cancer. 2005 May;43(1):83-94. doi: 10.1002/gcc.20170. Genes Chromosomes Cancer. 2005. PMID: 15723337

5

Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica.

Küry S, Kharfi M, Kamoun R, Taïeb A, Mallet E, Baudon JJ, Glastre C, Michel B, Sebag F, Brooks D, Schuster V, Scoul C, Dréno B, Bézieau S, Moisan JP. Küry S, et al. Among authors: scoul c. Hum Mutat. 2003 Oct;22(4):337-8. doi: 10.1002/humu.9178. Hum Mutat. 2003. PMID: 12955721

6

The Tunisian population history through the Crigler-Najjar type I syndrome.

Petit FM, Bézieau S, Gajdos V, Parisot F, Scoul C, Capel L, Stozinic V, Khrouf N, M'Rad R, Koshy A, Mollet-Boudjemline A, Francoual J, Labrune P. Petit FM, et al. Among authors: scoul c. Eur J Hum Genet. 2008 Jul;16(7):848-53. doi: 10.1038/sj.ejhg.5201989. Epub 2008 Jan 16. Eur J Hum Genet. 2008. PMID: 18197191

7

Purification of the recombinant human serotonin N-acetyltransferase (EC 2.3.1.87): further characterization of and comparison with AANAT from other species.

Ferry G, Ubeaud C, Dauly C, Mozo J, Guillard S, Berger S, Jimenez S, Scoul C, Leclerc G, Yous S, Delagrange P, Boutin JA. Ferry G, et al. Among authors: scoul c. Protein Expr Purif. 2004 Nov;38(1):84-98. doi: 10.1016/j.pep.2004.07.004. Protein Expr Purif. 2004. PMID: 15477086

8

New substrate analogues of human serotonin N-acetyltransferase produce in situ specific and potent inhibitors.

Ferry G, Ubeaud C, Mozo J, Péan C, Hennig P, Rodriguez M, Scoul C, Bonnaud A, Nosjean O, Galizzi JP, Delagrange P, Renard P, Volland JP, Yous S, Lesieur D, Boutin JA. Ferry G, et al. Among authors: scoul c. Eur J Biochem. 2004 Jan;271(2):418-28. doi: 10.1046/j.1432-1033.2003.03942.x. Eur J Biochem. 2004. PMID: 14717709 Free article.

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