BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 29986553)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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. Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men.
    Fedder J; Jørgensen MW; Engvad B
    Andrology; 2021 Mar; 9(2):588-598. PubMed ID: 33095972
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Association of cystic fibrosis transmembrane-conductance regulator gene mutation with negative outcome of intracytoplasmic sperm injection pregnancy in cases of congenital bilateral absence of vas deferens.
    Lu S; Cui Y; Li X; Zhang H; Liu J; Kong B; Cai F; Chen ZJ
    Fertil Steril; 2014 May; 101(5):1255-60. PubMed ID: 24559724
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Genetic diagnosis and sperm retrieval outcomes for Chinese patients with congenital bilateral absence of vas deferens.
    Wang H; An M; Liu Y; Hu K; Jin Y; Xu S; Chen B; Lu M
    Andrology; 2020 Sep; 8(5):1064-1069. PubMed ID: 32020786
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The role of SLC9A3 in Taiwanese patients with congenital bilateral absence of vas deferens (CBAVD).
    Chiang HS; Wang YY; Lin YH; Wu YN
    J Formos Med Assoc; 2019 Dec; 118(12):1576-1583. PubMed ID: 30797621
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa.
    Boudaya M; Fredj SH; Haj RB; Khrouf M; Bouker A; Halouani L; Messaoud T
    Ann Hum Biol; 2012 Jan; 39(1):76-9. PubMed ID: 22148899
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. The detection and significance of cystic fibrosis transmembrane conductance regulator gene promoter mutations in Chinese patients with congenital bilateral absence of the vas deferens.
    Bai S; Du Q; Liu X; Tong Y; Wu B
    Gene; 2018 Sep; 672():64-71. PubMed ID: 29864494
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review).
    Cui X; Wu X; Li Q; Jing X
    Mol Med Rep; 2020 Nov; 22(5):3587-3596. PubMed ID: 33000223
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.