BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 31845523)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 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. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens.
    Dörk T; Dworniczak B; Aulehla-Scholz C; Wieczorek D; Böhm I; Mayerova A; Seydewitz HH; Nieschlag E; Meschede D; Horst J; Pander HJ; Sperling H; Ratjen F; Passarge E; Schmidtke J; Stuhrmann M
    Hum Genet; 1997 Sep; 100(3-4):365-77. PubMed ID: 9272157
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens.
    Yang X; Sun Q; Yuan P; Liang H; Wu X; Lai L; Zhang Y
    Fertil Steril; 2015 Nov; 104(5):1268-75.e1-2. PubMed ID: 26277102
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations.
    Fang J; Wang X; Sun X; Cui Y; Diao F; Yang X
    Front Genet; 2022; 13():1035468. PubMed ID: 36437957
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mutation analysis of the cystic fibrosis transmembrane conductance regulator gene in Chinese congenital absence of vas deferens patients.
    Luo S; Feng J; Zhang Y; Yang X; Ma G; Hu T; Xi Y; Tu X; Wang C; Zhang H; Zou Z; Zhang Y
    Gene; 2021 Jan; 765():145045. PubMed ID: 32777524
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Male partners of infertile couples with congenital unilateral absence of the vas deferens are mainly non-azoospermic.
    Mieusset R; Bieth E; Daudin M; Isus F; Delaunay B; Bujan L; Monteil L; Fauquet I; Huyghe E; Hamdi SM
    Andrology; 2020 May; 8(3):645-653. PubMed ID: 31872980
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Significance of CFTR gene mutations in patients with congenital aplasia of vas deferens with special regard to renal aplasia.
    Schwarzer JU; Schwarz M
    Andrologia; 2012 Oct; 44(5):305-7. PubMed ID: 22340520
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens.
    Sharma N; Acharya N; Singh SK; Singh M; Sharma U; Prasad R
    Hum Reprod; 2009 May; 24(5):1229-36. PubMed ID: 19181743
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.