Fergelot P - Search Results

1

Le Gall JY, Jouanolle AM, Fergelot P, Mosser J, David V. Le Gall JY, et al. Among authors: fergelot p. Bull Acad Natl Med. 2004;188(2):247-62; discussion 262-3. Bull Acad Natl Med. 2004. PMID: 15506716 Review. French.

2

CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.

de Thonel A, Ahlskog JK, Daupin K, Dubreuil V, Berthelet J, Chaput C, Pires G, Leonetti C, Abane R, Barris LC, Leray I, Aalto AL, Naceri S, Cordonnier M, Benasolo C, Sanial M, Duchateau A, Vihervaara A, Puustinen MC, Miozzo F, Fergelot P, Lebigot É, Verloes A, Gressens P, Lacombe D, Gobbo J, Garrido C, Westerheide SD, David L, Petitjean M, Taboureau O, Rodrigues-Lima F, Passemard S, Sabéran-Djoneidi D, Nguyen L, Lancaster M, Sistonen L, Mezger V. de Thonel A, et al. Among authors: fergelot p. Nat Commun. 2022 Nov 16;13(1):7002. doi: 10.1038/s41467-022-34476-2. Nat Commun. 2022. PMID: 36385105 Free PMC article.

3

Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic population.

Dorval I, Fergelot P, Dubourg C, Jézéquel P, Chauvel B, Le Gall JY, Le Treut A. Dorval I, et al. Among authors: fergelot p. Clin Chem. 1994 Dec;40(12):2318-9. Clin Chem. 1994. PMID: 7527310 No abstract available.

4

Structural analysis of CFTR gene in congenital bilateral absence of vas deferens.

Jézéquel P, Dorval I, Fergelot P, Chauvel B, Le Treut A, Le Gall JY, Le Lannou D, Blayau M. Jézéquel P, et al. Among authors: fergelot p. Clin Chem. 1995 Jun;41(6 Pt 1):833-5. Clin Chem. 1995. PMID: 7539342

5

A human homologue to the yeast omnipotent suppressor 45 maps 100 kb centromeric to HLA-A.

Chauvel B, Dorval I, Fergelot P, Pichon L, Giffon T, Gicquel I, Le Gall JY, David V. Chauvel B, et al. Among authors: fergelot p. Immunogenetics. 1995;41(6):380-2. doi: 10.1007/BF00163996. Immunogenetics. 1995. PMID: 7759135 No abstract available.

6

French CF family genotype analysis shows that the R297Q mutation is a rare polymorphism.

Dorval I, Jézéquel P, Chauvel B, Dubourg C, Fergelot P, Le Gall JY, Roussey M, Blayau M. Dorval I, et al. Among authors: fergelot p. Hum Mutat. 1995;6(4):334-5. doi: 10.1002/humu.1380060407. Hum Mutat. 1995. PMID: 8680407

7

Haemochromatosis and HLA-H.

Jouanolle AM, Gandon G, Jézéquel P, Blayau M, Campion ML, Yaouanq J, Mosser J, Fergelot P, Chauvel B, Bouric P, Carn G, Andrieux N, Gicquel I, Le Gall JY, David V. Jouanolle AM, et al. Among authors: fergelot p. Nat Genet. 1996 Nov;14(3):251-2. doi: 10.1038/ng1196-251. Nat Genet. 1996. PMID: 8896550 No abstract available.

8

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

Jouanolle AM, Fergelot P, Gandon G, Yaouanq J, Le Gall JY, David V. Jouanolle AM, et al. Among authors: fergelot p. Hum Genet. 1997 Oct;100(5-6):544-7. doi: 10.1007/s004390050549. Hum Genet. 1997. PMID: 9341868

9

A 1200-kilobase transcription map encompassing the D6S105 locus at 6p21.3.

Mosser J, Andrieux N, Fergelot P, Gicquel I, Lelaure V, Galibert F, David V. Mosser J, et al. Among authors: fergelot p. Genomics. 1997 Dec 15;46(3):487-90. doi: 10.1006/geno.1997.5045. Genomics. 1997. PMID: 9441756

10

Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?

Jouanolle AM, Fergelot P, Raoul ML, Gandon G, Roussey M, Deugnier Y, Feingold J, Le Gall JY, David V. Jouanolle AM, et al. Among authors: fergelot p. Ann Genet. 1998;41(4):195-8. Ann Genet. 1998. PMID: 9881181

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