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 *

167 related articles for article (PubMed ID: 25386751)

  • 1. SNaPshot assay for the detection of the most common CFTR mutations in infertile men.
    Noveski P; Madjunkova S; Mircevska M; Plaseski T; Filipovski V; Plaseska-Karanfilska D
    PLoS One; 2014; 9(11):e112498. PubMed ID: 25386751
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia].
    Kusić J; Radojković D; Maletić V; Branković S; Savić A
    Srp Arh Celok Lek; 2002; 130(1-2):1-6. PubMed ID: 12073281
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure.
    Sharma H; Mavuduru RS; Singh SK; Prasad R
    Gene; 2014 Sep; 548(1):43-7. PubMed ID: 25010724
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular screening of the CFTR gene in Mexican patients with congenital absence of the vas deferens.
    Saldaña-Alvarez Y; Jiménez-Morales S; Echevarría-Sánchez M; Jiménez-Ruíz JL; García-Cavazos R; Velázquez-Cruz R; Carnevale A; Orozco L
    Genet Test Mol Biomarkers; 2012 Apr; 16(4):292-6. PubMed ID: 22103471
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian Population.
    Asadi F; Mirfakhraie R; Mirzajani F; Khedri A
    Iran Biomed J; 2019 Mar; 23(2):92-8. PubMed ID: 29986553
    [TBL] [Abstract][Full Text] [Related]  

  • 6. L138ins Variant of the
    Chernykh V; Sorokina T; Sedova A; Shtaut M; Solovova O; Marnat E; Adyan T; Beskorovaynaya T; Stepanova A; Shchagina O; Polyakov A
    Genes (Basel); 2023 Jul; 14(7):. PubMed ID: 37510311
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.
    Ghorbel M; Baklouti-Gargouri S; Keskes R; Sellami-Ben Hamida A; Feki-Chakroun N; Bahloul A; Fakhfakh F; Ammar-Keskes L
    Andrologia; 2012 May; 44 Suppl 1():376-82. PubMed ID: 21762191
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. 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]  

  • 13. 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]  

  • 14. The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.
    Safinejad K; Darbouy M; Kalantar SM; Zeinali S; Mirfakhraie R; Yadegar L; Houshmand M
    J Assist Reprod Genet; 2011 Nov; 28(11):1087-90. PubMed ID: 21976147
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Improved detection of cystic fibrosis mutations in infertility patients with DNA sequence analysis.
    Danziger KL; Black LD; Keiles SB; Kammesheidt A; Turek PJ
    Hum Reprod; 2004 Mar; 19(3):540-6. PubMed ID: 14998948
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The frequency and spectrum of mutations and the IVS8-T polymorphism of the CFTR gene in Russian infertile men].
    Chernykh VB; Stepanova AA; Beskorovaĭnaia TS; Sorokina TM; Shileĭko LV; Kurilo LF; Poliakov AV
    Genetika; 2010 Jun; 46(6):844-52. PubMed ID: 20734777
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia.
    Mak V; Zielenski J; Tsui LC; Durie P; Zini A; Martin S; Longley TB; Jarvi KA
    JAMA; 1999 Jun; 281(23):2217-24. PubMed ID: 10376575
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rational approach to genetic testing of cystic fibrosis (CF) in infertile men.
    Mennicke K; Klingenberg RD; Bals-Pratsch M; Diedrich K; Schwinger E
    Andrologia; 2005 Feb; 37(1):1-9. PubMed ID: 15644056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.