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Journal Abstract Search

765 related items for PubMed ID: 10645285

  • 1. 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
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  • 3. 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
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  • 4. 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
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  • 5. 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 Jul; 40(1):5-9. PubMed ID: 9150843
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  • 9. 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 01; 332(22):1475-80. PubMed ID: 7739684
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  • 10. CFTR mutations and polymorphisms in male infertility.
    Cuppens H, Cassiman JJ.
    Int J Androl; 2004 Oct 01; 27(5):251-6. PubMed ID: 15379964
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  • 11. Congenital absence of vas deferens and cystic fibrosis.
    Leonardi S, Bombace V, Rotolo N, Sciuto C, La Rosa M.
    Minerva Pediatr; 2003 Feb 01; 55(1):43-7, 47-50. PubMed ID: 12660625
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  • 14. 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 Feb 01; 16(2):143-56. PubMed ID: 10923036
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  • 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 Feb 01; 12(3):213-4. PubMed ID: 10651488
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  • 18. 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 01; 76(3):282-6. PubMed ID: 19737283
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  • 20. Urogenital anomalies in men with congenital absence of the vas deferens.
    Schlegel PN, Shin D, Goldstein M.
    J Urol; 1996 May 01; 155(5):1644-8. PubMed ID: 8627844
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