154 related articles for article (PubMed ID: 28805948)
1. Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population.
Yang B; Wang J; Zhang W; Pan H; Li T; Liu B; Li H; Wang B
Andrology; 2017 Sep; 5(5):954-957. PubMed ID: 28805948
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.
Wu H; Gao Y; Ma C; Shen Q; Wang J; Lv M; Liu C; Cheng H; Zhu F; Tian S; Elshewy N; Ni X; Tan Q; Xu X; Zhou P; Wei Z; Zhang F; He X; Cao Y
J Assist Reprod Genet; 2020 Jun; 37(6):1421-1429. PubMed ID: 32314195
[TBL] [Abstract][Full Text] [Related]
4. Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.
Patat O; Pagin A; Siegfried A; Mitchell V; Chassaing N; Faguer S; Monteil L; Gaston V; Bujan L; Courtade-Saïdi M; Marcelli F; Lalau G; Rigot JM; Mieusset R; Bieth E
Am J Hum Genet; 2016 Aug; 99(2):437-42. PubMed ID: 27476656
[TBL] [Abstract][Full Text] [Related]
5. Compound heterozygous mutations in CFTR causing CBAVD in Chinese pedigrees.
Yang B; Wang X; Zhang W; Li H; Wang B
Mol Genet Genomic Med; 2018 Nov; 6(6):1097-1103. PubMed ID: 30450785
[TBL] [Abstract][Full Text] [Related]
6. Novel ADGRG2 truncating variants in patients with X-linked congenital absence of vas deferens.
Pagin A; Bergougnoux A; Girodon E; Reboul MP; Willoquaux C; Kesteloot M; Raynal C; Bienvenu T; Humbert M; Lalau G; Bieth E
Andrology; 2020 May; 8(3):618-624. PubMed ID: 31845523
[TBL] [Abstract][Full Text] [Related]
7. Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles.
Yuan P; Liang ZK; Liang H; Zheng LY; Li D; Li J; Zhang J; Tian J; Lai LH; Zhang K; He ZY; Zhang QX; Wang WJ
Andrology; 2019 May; 7(3):329-340. PubMed ID: 30811104
[TBL] [Abstract][Full Text] [Related]
8. Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens.
Cheng H; Yang S; Meng Q; Zheng B; Gu Y; Wang L; Song T; Xu C; Wang G; Han M; Shen L; Ding J; Li H; Ouyang J
J Assist Reprod Genet; 2022 Mar; 39(3):719-728. PubMed ID: 35119551
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
11. A novel mutation (-195C>A) in the promoter region of CFTR gene is associated with Chinese Congenital Bilateral Absence of Vas Deferens (CBAVD).
Feng J; Wu X; Zhang Y; Yang X; Ma G; Chen S; Luo S; Zhang Y
Gene; 2019 Nov; 719():144007. PubMed ID: 31357024
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Genetics of the congenital absence of the vas deferens.
Bieth E; Hamdi SM; Mieusset R
Hum Genet; 2021 Jan; 140(1):59-76. PubMed ID: 32025909
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD.
Ma C; Wang R; Li T; Li H; Wang B
Mol Genet Genomic Med; 2020 Nov; 8(11):e1506. PubMed ID: 32951344
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Homozygous 5T alleles, clinical presentation and genetic analysis within a family with congenital bilateral absence of the vas deferens].
Feng JR; Zhang YN; Wu X; Yang XJ; Chen ST; Ma GC; Luo SG; Zhang Y
Zhonghua Yi Xue Za Zhi; 2018 May; 98(18):1414-1418. PubMed ID: 29804404
[No Abstract] [Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]