249 related articles for article (PubMed ID: 28384194)
1. Loss of SLC9A3 decreases CFTR protein and causes obstructed azoospermia in mice.
Wang YY; Lin YH; Wu YN; Chen YL; Lin YC; Cheng CY; Chiang HS
PLoS Genet; 2017 Apr; 13(4):e1006715. PubMed ID: 28384194
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. SLC9A3 Affects Vas Deferens Development and Associates with Taiwanese Congenital Bilateral Absence of the Vas Deferens.
Wu YN; Chen KC; Wu CC; Lin YH; Chiang HS
Biomed Res Int; 2019; 2019():3562719. PubMed ID: 30956978
[TBL] [Abstract][Full Text] [Related]
4. SLC9A3 Protein Is Critical for Acrosomal Formation in Postmeiotic Male Germ Cells.
Wang YY; Chiang HS; Cheng CY; Wu YN; Lin YC; Liu HC; Tsai WK; Chen YL; Lin YH
Int J Mol Sci; 2017 Dec; 19(1):. PubMed ID: 29286340
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. 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]
8. Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†.
Tan MQ; Huang WJ; Lan FH; Xu YJ; Zheng MY; Tang Y
Biol Reprod; 2022 Jan; 106(1):108-117. PubMed ID: 34673937
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. [Gene mutations in congenital bilateral absence of the vas deferens: An update].
Tan MQ; Tang Y
Zhonghua Nan Ke Xue; 2021 May; 27(5):450-455. PubMed ID: 34914322
[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. [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]
17. CFTR mutations and polymorphisms in male infertility.
Cuppens H; Cassiman JJ
Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964
[TBL] [Abstract][Full Text] [Related]
18. 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]
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. 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]
[Next] [New Search]
