BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 9150843)

  • 1. Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patients.
    Bienvenu T; Adjiman M; Thiounn N; Jeanpierre M; Hubert D; Lepercoq J; Francoual C; Wolf J; Izard V; Jouannet P; Kaplan JC; Beldjord C
    Ann Genet; 1997; 40(1):5-9. PubMed ID: 9150843
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R; Gilani MA; Gourabi H; Dizaj AV; Mollamohamadi S
    Mol Hum Reprod; 2006 Jul; 12(7):469-73. PubMed ID: 16714368
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.
    Chillón M; Casals T; Mercier B; Bassas L; Lissens W; Silber S; Romey MC; Ruiz-Romero J; Verlingue C; Claustres M
    N Engl J Med; 1995 Jun; 332(22):1475-80. PubMed ID: 7739684
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].
    Bienvenu T; Claustres M
    Contracept Fertil Sex; 1996 Jun; 24(6):495-500. PubMed ID: 8766513
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype.
    Radpour R; Gourabi H; Gilani MA; Dizaj AV
    J Androl; 2008; 29(1):35-40. PubMed ID: 17673436
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.
    Claustres M; Guittard C; Bozon D; Chevalier F; Verlingue C; Ferec C; Girodon E; Cazeneuve C; Bienvenu T; Lalau G; Dumur V; Feldmann D; Bieth E; Blayau M; Clavel C; Creveaux I; Malinge MC; Monnier N; Malzac P; Mittre H; Chomel JC; Bonnefont JP; Iron A; Chery M; Georges MD
    Hum Mutat; 2000; 16(2):143-56. PubMed ID: 10923036
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens.
    Grangeia A; Niel F; Carvalho F; Fernandes S; Ardalan A; Girodon E; Silva J; Ferrás L; Sousa M; Barros A
    Hum Reprod; 2004 Nov; 19(11):2502-8. PubMed ID: 15333598
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular study of (TG)m(T)n polymorphisms in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R; Gourabi H; Gilani MA; Dizaj AV
    J Androl; 2007; 28(4):541-7. PubMed ID: 17314234
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic findings in congenital bilateral aplasia of vas deferens patients and identification of six novel mutatations. Mutations in brief no. 138. Online.
    de Meeus A; Guittard C; Desgeorges M; Carles S; Demaille J; Claustres M
    Hum Mutat; 1998; 11(6):480. PubMed ID: 10200050
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R; Gourabi H; Gilani MA; Dizaj AV; Rezaee M; Mollamohamadi S
    Mol Hum Reprod; 2006 Nov; 12(11):717-21. PubMed ID: 16973827
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.
    Ratbi I; Legendre M; Niel F; Martin J; Soufir JC; Izard V; Costes B; Costa C; Goossens M; Girodon E
    Hum Reprod; 2007 May; 22(5):1285-91. PubMed ID: 17329263
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CFTR mutations and polymorphisms in male infertility.
    Cuppens H; Cassiman JJ
    Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens.
    Ravnik-Glavac M; Dean M; Glavac D
    Pflugers Arch; 2000; 439(3 Suppl):R53-5. PubMed ID: 10653141
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.
    Dayangaç D; Erdem H; Yilmaz E; Sahin A; Sohn C; Ozgüç M; Dörk T
    Hum Reprod; 2004 May; 19(5):1094-100. PubMed ID: 15070876
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expression of the cystic fibrosis transmembrane conductance regulator (CFTR) mRNA in normal and pathological adult human epididymis.
    Patrizio P; Salameh WA
    J Reprod Fertil Suppl; 1998; 53():261-70. PubMed ID: 10645285
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation associated with a congenital bilateral absence of vas deferens.
    Sakamoto H; Yajima T; Suzuki K; Ogawa Y
    Int J Urol; 2008 Mar; 15(3):270-1. PubMed ID: 18304229
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. Online.
    Bienvenu T; Bousquet S; Vidaud D; Hubert D; Francoual C; Beldjord C; Kaplan JC
    Hum Mutat; 1998; 12(3):213-4. PubMed ID: 10651488
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility.
    Radpour R; Gourabi H; Dizaj AV; Holzgreve W; Zhong XY
    J Androl; 2008; 29(5):506-13. PubMed ID: 18567645
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens.
    Grangeia A; Carvalho F; Fernandes S; Silva J; Sousa M; Barros A
    Fertil Steril; 2005 Feb; 83(2):448-51. PubMed ID: 15705389
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CFTR (TG)m(T)n polymorphism in patients with CBAVD in a population expressing low incidence of cystic fibrosis.
    Chiang HS; Lu JF; Liu CH; Wu YN; Wu CC
    Clin Genet; 2009 Sep; 76(3):282-6. PubMed ID: 19737283
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.