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 *

152 related articles for article (PubMed ID: 23214250)

  • 1. [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]  

  • 2. 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]  

  • 3. [Association of CFTR gene polymorphism with congenital bilateral absence of vas deferens in ethnic Han Chinese patients].
    Liu LJ; Li HG; Gu X; Zhu JW; Zhao K; Tang YP; Xiong CL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):729-32. PubMed ID: 24327157
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.
    Li H; Wen Q; Li H; Zhao L; Zhang X; Wang J; Cheng L; Yang J; Chen S; Ma X; Wang B
    J Cyst Fibros; 2012 Jul; 11(4):316-23. PubMed ID: 22483971
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens.
    Gaikwad A; Khan S; Kadam S; Kadam K; Dighe V; Shah R; Kulkarni V; Kumaraswamy R; Gajbhiye R
    Andrologia; 2018 Mar; 50(2):. PubMed ID: 28776713
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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. 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]  

  • 11. CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis.
    Yu J; Chen Z; Ni Y; Li Z
    Hum Reprod; 2012 Jan; 27(1):25-35. PubMed ID: 22081250
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens.
    Wu CC; Alper OM; Lu JF; Wang SP; Guo L; Chiang HS; Wong LJ
    Hum Reprod; 2005 Sep; 20(9):2470-5. PubMed ID: 15905293
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. [Detection of promoter region of CFTR gene in Chinese congenital bilateral absence of vas deferens].
    Wu X; Zhang Y; Yang X; Chen S; Yuan P; Zhang B
    Zhonghua Yi Xue Za Zhi; 2015 Sep; 95(36):2914-8. PubMed ID: 26814065
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree.
    Li L; Qu X; Cui C; Feng K; Xia Y; Wan F; Ge H; Fang Y; Zhang C; Guo H
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2364. PubMed ID: 38284450
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [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]  

    [Next]    [New Search]
    of 8.