Férec C - Search Results

1

The PROPKD Score: A New Algorithm to Predict Renal Survival in Autosomal Dominant Polycystic Kidney Disease.

Cornec-Le Gall E, Audrézet MP, Rousseau A, Hourmant M, Renaudineau E, Charasse C, Morin MP, Moal MC, Dantal J, Wehbe B, Perrichot R, Frouget T, Vigneau C, Potier J, Jousset P, Guillodo MP, Siohan P, Terki N, Sawadogo T, Legrand D, Menoyo-Calonge V, Benarbia S, Besnier D, Longuet H, Férec C, Le Meur Y. Cornec-Le Gall E, et al. Among authors: ferec c. J Am Soc Nephrol. 2016 Mar;27(3):942-51. doi: 10.1681/ASN.2015010016. Epub 2015 Jul 6. J Am Soc Nephrol. 2016. PMID: 26150605 Free PMC article.

2

A polymorphism in intron 20 of the CFTR gene.

Quere I, Guillermit H, Mercier B, Audrezet MP, Ferec C. Quere I, et al. Among authors: ferec c. Nucleic Acids Res. 1991 Oct 11;19(19):5453. doi: 10.1093/nar/19.19.5453-a. Nucleic Acids Res. 1991. PMID: 1717950 Free PMC article.

3

Identification of three novel mutations (457 TAT-->G, D192G, Q685X) in the Slovenian CF patients.

Audrézet MP, Canki-Klain N, Mercier B, Bracar D, Verlingue C, Férec C. Audrézet MP, et al. Among authors: ferec c. Hum Genet. 1994 Jun;93(6):659-62. doi: 10.1007/BF00201566. Hum Genet. 1994. PMID: 7516305

4

Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.

Mercier B, Verlingue C, Lissens W, Silber SJ, Novelli G, Bonduelle M, Audrézet MP, Férec C. Mercier B, et al. Among authors: ferec c. Am J Hum Genet. 1995 Jan;56(1):272-7. Am J Hum Genet. 1995. PMID: 7529962 Free PMC article.

5

Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->A.

Mercier B, Audrézet MP, Feigelson J, Douchain F, Raguénès O, Verlingue C, Quéré I, Férec C. Mercier B, et al. Among authors: ferec c. Hum Mutat. 1994;4(3):224-6. doi: 10.1002/humu.1380040309. Hum Mutat. 1994. PMID: 7530553 No abstract available.

6

Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel alleles.

Verlingue C, Kapranov NI, Mercier B, Ginter EK, Petrova NV, Audrezet MP, Férec C. Verlingue C, et al. Among authors: ferec c. Hum Mutat. 1995;5(3):205-9. doi: 10.1002/humu.1380050304. Hum Mutat. 1995. PMID: 7541273

7

Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patients.

Férec C, Novelli G, Verlingue C, Quéré I, Dallapiccola B, Audrézet MP, Mercier B. Férec C, et al. Mol Cell Probes. 1995 Apr;9(2):135-7. doi: 10.1016/s0890-8508(95)80038-7. Mol Cell Probes. 1995. PMID: 7541510

8

Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delT.

Mercier B, Lissens W, Audrézet MP, Bonduelle M, Quéré I, Hilbert P, Liebaers I, Férec C. Mercier B, et al. Among authors: ferec c. Hum Mutat. 1995;6(2):188-9. doi: 10.1002/humu.1380060215. Hum Mutat. 1995. PMID: 7581406 No abstract available.

9

A novel mutation in exon 3 of the CFTR gene.

Guillermit H, Jéhanne M, Quéré I, Audrézet MP, Mercier B, Férec C. Guillermit H, et al. Among authors: ferec c. Hum Genet. 1993 Apr;91(3):233-5. doi: 10.1007/BF00218262. Hum Genet. 1993. PMID: 7682984

10

Identification of 12 novel mutations in the CFTR gene.

Audrézet MP, Mercier B, Guillermit H, Quéré I, Verlingue C, Rault G, Férec C. Audrézet MP, et al. Among authors: ferec c. Hum Mol Genet. 1993 Jan;2(1):51-4. doi: 10.1093/hmg/2.1.51. Hum Mol Genet. 1993. PMID: 7683952

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