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 *

193 related articles for article (PubMed ID: 29986553)

  • 61. [Detection of CFTR gene mutations in azoospermia patients with congenital unilateral absence of the vas deferens].
    Yang XJ; Yuan P; Wu X; Zhang H; He QQ; Zhang Y
    Zhonghua Nan Ke Xue; 2015 Mar; 21(3):229-33. PubMed ID: 25898554
    [TBL] [Abstract][Full Text] [Related]  

  • 62. The CFTR M470V, intron 8 poly-T, and 8 TG-repeats detection in Chinese males with congenital bilateral absence of the vas deferens.
    Du Q; Li Z; Pan Y; Liu X; Pan B; Wu B
    Biomed Res Int; 2014; 2014():689185. PubMed ID: 24551851
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Cystic fibrosis mutation screening in healthy men with reduced sperm quality.
    van der Ven K; Messer L; van der Ven H; Jeyendran RS; Ober C
    Hum Reprod; 1996 Mar; 11(3):513-7. PubMed ID: 8671256
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Detection of the mutation of all the exons of the CFTR gene in Chinese men with congenital bilateral absence of the vas deferens].
    Du Q; Fang YY; Pan YF; Pan BC; Song YS; Wu B
    Zhonghua Nan Ke Xue; 2012 Nov; 18(11):999-1003. PubMed ID: 23214250
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Genetic findings in congenital bilateral aplasia of vas deferens patients and identification of six novel mutatations. Mutations in brief no. 138. Online.
    de Meeus A; Guittard C; Desgeorges M; Carles S; Demaille J; Claustres M
    Hum Mutat; 1998; 11(6):480. PubMed ID: 10200050
    [TBL] [Abstract][Full Text] [Related]  

  • 66. CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study.
    Jiang L; Jin J; Wang S; Zhang F; Dai Y; Shi L; Zhang S
    Gene; 2017 Aug; 626():282-289. PubMed ID: 28456595
    [TBL] [Abstract][Full Text] [Related]  

  • 67. CFTR (TG)m(T)n polymorphism in patients with CBAVD in a population expressing low incidence of cystic fibrosis.
    Chiang HS; Lu JF; Liu CH; Wu YN; Wu CC
    Clin Genet; 2009 Sep; 76(3):282-6. PubMed ID: 19737283
    [TBL] [Abstract][Full Text] [Related]  

  • 68. 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]  

  • 69. [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]  

  • 70. Mutation frequency of cystic fibrosis transmembrane regulator is not increased in oligozoospermic male candidates for intracytoplasmic sperm injection.
    Tuerlings JH; Mol B; Kremer JA; Looman M; Meuleman EJ; te Meerman GJ; Buys CH; Merkus HM; Scheffer H
    Fertil Steril; 1998 May; 69(5):899-903. PubMed ID: 9591500
    [TBL] [Abstract][Full Text] [Related]  

  • 71. 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]  

  • 72. Cystic fibrosis gene mutations and polymorphisms in Saudi men with infertility.
    AlMaghamsi T; Iqbal N; Al-Esaei NA; Mohammed M; Eddin KZ; Ghurab F; Moghrabi N; Heaphy E; Junaid I
    Ann Saudi Med; 2020; 40(4):321-329. PubMed ID: 32757986
    [TBL] [Abstract][Full Text] [Related]  

  • 73. A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens.
    Grangeia A; Carvalho F; Fernandes S; Silva J; Sousa M; Barros A
    Fertil Steril; 2005 Feb; 83(2):448-51. PubMed ID: 15705389
    [TBL] [Abstract][Full Text] [Related]  

  • 74. 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]  

  • 75. CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.
    Thauvin-Robinet C; Munck A; Huet F; de Becdelièvre A; Jimenez C; Lalau G; Gautier E; Rollet J; Flori J; Nové-Josserand R; Soufir JC; Haloun A; Hubert D; Houssin E; Bellis G; Rault G; David A; Janny L; Chiron R; Rives N; Hairion D; Collignon P; Valeri A; Karsenty G; Rossi A; Audrézet MP; Férec C; Leclerc J; Georges Md; Claustres M; Bienvenu T; Gérard B; Boisseau P; Cabet-Bey F; Cheillan D; Feldmann D; Clavel C; Bieth E; Iron A; Simon-Bouy B; Izard V; Steffann J; Viville S; Costa C; Drouineaud V; Fauque P; Binquet C; Bonithon-Kopp C; Morris MA; Faivre L; Goossens M; Roussey M; Girodon E;
    J Med Genet; 2013 Apr; 50(4):220-7. PubMed ID: 23378603
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling.
    Daudin M; Bieth E; Bujan L; Massat G; Pontonnier F; Mieusset R
    Fertil Steril; 2000 Dec; 74(6):1164-74. PubMed ID: 11119745
    [TBL] [Abstract][Full Text] [Related]  

  • 77. CFTR gene mutations in Japanese individuals with congenital bilateral absence of the vas deferens.
    Anzai C; Morokawa N; Okada H; Kamidono S; Eto Y; Yoshimura K
    J Cyst Fibros; 2003 Mar; 2(1):14-8. PubMed ID: 15463840
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.
    De Braekeleer M; Férec C
    Mol Hum Reprod; 1996 Sep; 2(9):669-77. PubMed ID: 9239681
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Immunohystochemical analysis of CFTR in normal and disrupted spermatogenesis.
    Teixeira S; Sá R; Grangeia A; Silva J; Oliveira C; Ferráz L; Alves A; Paiva S; Barros A; Sousa M
    Syst Biol Reprod Med; 2013 Feb; 59(1):53-9. PubMed ID: 22989055
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina.
    Timmreck LS; Gray MR; Handelin B; Allito B; Rohlfs E; Davis AJ; Gidwani G; Reindollar RH
    Am J Med Genet A; 2003 Jul; 120A(1):72-6. PubMed ID: 12794695
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.