These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 7513294)

  • 1. Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens.
    Culard JF; Desgeorges M; Costa P; Laussel M; Razakatzara G; Navratil H; Demaille J; Claustres M
    Hum Genet; 1994 Apr; 93(4):467-70. PubMed ID: 7513294
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Congenital agenesis of the vas deferens and cystic fibrosis].
    Kugler A; Laccone F; Weidner W; Kallerhoff M
    Urologe A; 1995 Jul; 34(4):348-50. PubMed ID: 7545847
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia.
    Kanavakis E; Tzetis M; Antoniadi T; Pistofidis G; Milligos S; Kattamis C
    Mol Hum Reprod; 1998 Apr; 4(4):333-7. PubMed ID: 9620832
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected.
    Casals T; Bassas L; Ruiz-Romero J; Chillón M; Giménez J; Ramos MD; Tapia G; Narváez H; Nunes V; Estivill X
    Hum Genet; 1995 Feb; 95(2):205-11. PubMed ID: 7532150
    [TBL] [Abstract][Full Text] [Related]  

  • 5. CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens.
    Rave-Harel N; Madgar I; Goshen R; Nissim-Rafinia M; Ziadni A; Rahat A; Chiba O; Kalman YM; Brautbar C; Levinson D
    Am J Hum Genet; 1995 Jun; 56(6):1359-66. PubMed ID: 7539210
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A T3 allele in the CFTR gene exacerbates exon 9 skipping in vas deferens and epididymal cell lines and is associated with Congenital Bilateral Absence of Vas Deferens (CBAVD).
    Disset A; Michot C; Harris A; Buratti E; Claustres M; Tuffery-Giraud S
    Hum Mutat; 2005 Jan; 25(1):72-81. PubMed ID: 15580565
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities.
    Lissens W; Mercier B; Tournaye H; Bonduelle M; Férec C; Seneca S; Devroey P; Silber S; Van Steirteghem A; Liebaers I
    Hum Reprod; 1996 Dec; 11 Suppl 4():55-78; discussion 79-80. PubMed ID: 9147111
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic fibrosis mutation screening in healthy men with reduced sperm quality.
    van der Ven K; Messer L; van der Ven H; Jeyendran RS; Ober C
    Hum Reprod; 1996 Mar; 11(3):513-7. PubMed ID: 8671256
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.
    De Braekeleer M; Férec C
    Mol Hum Reprod; 1996 Sep; 2(9):669-77. PubMed ID: 9239681
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies.
    Gajbhiye R; Kadam K; Khole A; Gaikwad A; Kadam S; Shah R; Kumaraswamy R; Khole V
    Indian J Med Res; 2016 May; 143(5):616-23. PubMed ID: 27488005
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Mutations of the cystic fibrosis gene and congenital absence of the vas deferens.
    Patrizio P; Leonard DG
    Results Probl Cell Differ; 2000; 28():175-86. PubMed ID: 10626298
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Mutation frequency of cystic fibrosis transmembrane regulator is not increased in oligozoospermic male candidates for intracytoplasmic sperm injection.
    Tuerlings JH; Mol B; Kremer JA; Looman M; Meuleman EJ; te Meerman GJ; Buys CH; Merkus HM; Scheffer H
    Fertil Steril; 1998 May; 69(5):899-903. PubMed ID: 9591500
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Cystic fibrosis gene mutations do not affect sperm function during in vitro fertilization with micromanipulation for men with bilateral congenital absence of vas deferens.
    Schlegel PN; Cohen J; Goldstein M; Alikani M; Adler A; Gilbert BR; Palermo GD; Rosenwaks Z
    Fertil Steril; 1995 Aug; 64(2):421-6. PubMed ID: 7542209
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.