Férec C - Search Results

1

A novel missense mutation in SLC40A1 results in resistance to hepcidin and confirms the existence of two ferroportin-associated iron overload diseases.

Létocart E, Le Gac G, Majore S, Ka C, Radio FC, Gourlaouen I, De Bernardo C, Férec C, Grammatico P. Létocart E, et al. Among authors: ferec c. Br J Haematol. 2009 Nov;147(3):379-85. doi: 10.1111/j.1365-2141.2009.07834.x. Epub 2009 Aug 25. Br J Haematol. 2009. PMID: 19709084 Free article.

2

Clinical and molecular aspects of juvenile hemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, canada).

Rivard SR, Mura C, Simard H, Simard R, Grimard D, Le Gac G, Raguenes O, Férec C, De Braekeleer M. Rivard SR, et al. Among authors: ferec c. Blood Cells Mol Dis. 2000 Feb;26(1):10-4. doi: 10.1006/bcmd.2000.0271. Blood Cells Mol Dis. 2000. PMID: 10772871

3

Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada).

Rivard SR, Mura C, Simard H, Simard R, Grimard D, Le Gac G, Raguenes O, Férec C, De Braekeleer M. Rivard SR, et al. Among authors: ferec c. Br J Haematol. 2000 Mar;108(4):854-8. doi: 10.1046/j.1365-2141.2000.01954.x. Br J Haematol. 2000. PMID: 10792295 Free article.

4

Relation between HFE mutations and mild iron-overload expression.

Mura C, Le Gac G, Raguénes O, Mercier AY, Le Guen A, Férec C. Mura C, et al. Among authors: ferec c. Mol Genet Metab. 2000 Apr;69(4):295-301. doi: 10.1006/mgme.2000.2981. Mol Genet Metab. 2000. PMID: 10870847

5

Nramp2 analysis in hemochromatosis probands.

Le Gac G, Mura C, Raguenes O, Mercier AY, de Braekeleer M, Férec C. Le Gac G, et al. Among authors: ferec c. Blood Cells Mol Dis. 2000 Aug;26(4):312-9. doi: 10.1006/bcmd.2000.0312. Blood Cells Mol Dis. 2000. PMID: 11042033

6

Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC.

Le Gac G, Mura C, Férec C. Le Gac G, et al. Among authors: ferec c. Clin Chem. 2001 Sep;47(9):1633-40. Clin Chem. 2001. PMID: 11514397

7

Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect.

Le Gac G, Dupradeau FY, Mura C, Jacolot S, Scotet V, Esnault G, Mercier AY, Rochette J, Férec C. Le Gac G, et al. Among authors: ferec c. Blood Cells Mol Dis. 2003 May-Jun;30(3):231-7. doi: 10.1016/s1079-9796(03)00036-6. Blood Cells Mol Dis. 2003. PMID: 12737937

8

Hereditary hemochromatosis: effect of excessive alcohol consumption on disease expression in patients homozygous for the C282Y mutation.

Scotet V, Mérour MC, Mercier AY, Chanu B, Le Faou T, Raguénes O, Le Gac G, Mura C, Nousbaum JB, Férec C. Scotet V, et al. Among authors: ferec c. Am J Epidemiol. 2003 Jul 15;158(2):129-34. doi: 10.1093/aje/kwg123. Am J Epidemiol. 2003. PMID: 12851225

9

HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype.

Jacolot S, Le Gac G, Scotet V, Quere I, Mura C, Ferec C. Jacolot S, et al. Among authors: ferec c. Blood. 2004 Apr 1;103(7):2835-40. doi: 10.1182/blood-2003-10-3366. Epub 2003 Dec 11. Blood. 2004. PMID: 14670915 Free article.

10

Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.

Le Gac G, Mons F, Jacolot S, Scotet V, Férec C, Frébourg T. Le Gac G, et al. Among authors: ferec c. Br J Haematol. 2004 Jun;125(5):674-8. doi: 10.1111/j.1365-2141.2004.04950.x. Br J Haematol. 2004. PMID: 15147384 Free article.

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