BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 29986553)

  • 21. [Association of CFTR gene polymorphism with congenital bilateral absence of vas deferens in ethnic Han Chinese patients].
    Liu LJ; Li HG; Gu X; Zhu JW; Zhao K; Tang YP; Xiong CL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):729-32. PubMed ID: 24327157
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens.
    Ni WH; Jiang L; Fei QJ; Jin JY; Yang X; Huang XF
    Asian J Androl; 2012 Sep; 14(5):687-90. PubMed ID: 22842702
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens.
    Gaikwad A; Khan S; Kadam S; Kadam K; Dighe V; Shah R; Kulkarni V; Kumaraswamy R; Gajbhiye R
    Andrologia; 2018 Mar; 50(2):. PubMed ID: 28776713
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cystic fibrosis transmembrane conductance regulator gene mutations in infertile males with congenital bilateral absence of the vas deferens.
    Uzun S; Gökçe S; Wagner K
    Tohoku J Exp Med; 2005 Dec; 207(4):279-85. PubMed ID: 16272798
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia.
    Jafari L; Safinejad K; Nasiri M; Heidari M; Houshmand M
    J Med Life; 2022 Apr; 15(4):547-556. PubMed ID: 35646184
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Different cystic fibrosis transmembrane conductance regulator mutations in Chinese men with congenital bilateral absence of vas deferens and other acquired obstructive azoospermia.
    Lu S; Yang X; Cui Y; Li X; Zhang H; Liu J; Chen ZJ
    Urology; 2013 Oct; 82(4):824-8. PubMed ID: 23953609
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree.
    Li L; Qu X; Cui C; Feng K; Xia Y; Wan F; Ge H; Fang Y; Zhang C; Guo H
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2364. PubMed ID: 38284450
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis.
    Yu J; Chen Z; Ni Y; Li Z
    Hum Reprod; 2012 Jan; 27(1):25-35. PubMed ID: 22081250
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.
    de Souza DAS; Faucz FR; Pereira-Ferrari L; Sotomaior VS; Raskin S
    Andrology; 2018 Jan; 6(1):127-135. PubMed ID: 29216686
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Involvement of CFTR gene alterations in obstructive and nonobstructive infertility in men.
    Ravnik-Glavac M; Svetina N; Zorn B; Peterlin B; Glavac D
    Genet Test; 2001; 5(3):243-7. PubMed ID: 11788091
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
    Sharma H; Mavuduru RS; Singh SK; Prasad R
    Mol Hum Reprod; 2014 Sep; 20(9):827-35. PubMed ID: 24958810
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The association between variants in the CFTR gene and nonobstructive male infertility: A meta-analysis.
    Yang L; Ren Z; Yang B; Zhou J; Peng Z; Fang K; Wang L; Liu S; Lu D; Dong Q
    Andrologia; 2020 Mar; 52(2):e13475. PubMed ID: 31820482
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens.
    Ge B; Zhang M; Wang R; Wang D; Li T; Li H; Wang B
    J Assist Reprod Genet; 2019 Dec; 36(12):2541-2545. PubMed ID: 31709488
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Correlation between CFTR 5T polymorphisms and the risk of congenital bilateral absence of the vas deferens].
    Zhao GG; Sun HB; Zhi HJ; Wang F; Wu QY; Xia XY; Xu XF
    Zhonghua Nan Ke Xue; 2019 Mar; 25(3):231-237. PubMed ID: 32216241
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens.
    Wu CC; Alper OM; Lu JF; Wang SP; Guo L; Chiang HS; Wong LJ
    Hum Reprod; 2005 Sep; 20(9):2470-5. PubMed ID: 15905293
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [The analysis of CFTR mutations in men with azoospermia, oligozoospermia and asthenozoospermia].
    Slezak R; Szczepaniak M; Pasińska M; Czemarmazowicz H
    Ginekol Pol; 2007 Aug; 78(8):605-10. PubMed ID: 18050608
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.
    Li H; Wen Q; Li H; Zhao L; Zhang X; Wang J; Cheng L; Yang J; Chen S; Ma X; Wang B
    J Cyst Fibros; 2012 Jul; 11(4):316-23. PubMed ID: 22483971
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.