192 related articles for article (PubMed ID: 29986553)
41. 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]
42. Cystic fibrosis transmembrane conductance regulator-related male infertility: Relevance of genetic testing & counselling in Indian population.
Gaikwad A; Khan S; Kadam S; Shah R; Kulkarni V; Kumaraswamy R; Kadam K; Dighe V; Gajbhiye R
Indian J Med Res; 2020 Dec; 152(6):575-583. PubMed ID: 34145097
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols.
Giuliani R; Antonucci I; Torrente I; Grammatico P; Palka G; Stuppia L
Asian J Androl; 2010 Nov; 12(6):819-26. PubMed ID: 20657600
[TBL] [Abstract][Full Text] [Related]
45. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected.
Casals T; Bassas L; Ruiz-Romero J; Chillón M; Giménez J; Ramos MD; Tapia G; Narváez H; Nunes V; Estivill X
Hum Genet; 1995 Feb; 95(2):205-11. PubMed ID: 7532150
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.
Fathy M; Ramzy T; Elmonem MA; Amer M; Zeidan A; Hassan FA; Mehaney DA
Andrologia; 2016 Dec; 48(10):1307-1312. PubMed ID: 26989879
[TBL] [Abstract][Full Text] [Related]
48. Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variants.
Sachdeva K; Saxena R; Majumdar A; Chadha S; Verma IC
Genet Test Mol Biomarkers; 2011 May; 15(5):307-12. PubMed ID: 21254931
[TBL] [Abstract][Full Text] [Related]
49. Loss-of-function
Hou JW; Li XL; Wang L; Dai CL; Li N; Jiang XH; Tan YQ; Tian EP; Li QT; Xu WM
Asian J Androl; 2023; 25(1):58-65. PubMed ID: 35665694
[TBL] [Abstract][Full Text] [Related]
50. 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]
51. Diagnostics of CFTR-negative patients with congenital bilateral absence of vas deferens: which mutations are of most interest?
Ferlin A; Stuppia L
Expert Rev Mol Diagn; 2020 Mar; 20(3):265-267. PubMed ID: 31854215
[No Abstract] [Full Text] [Related]
52. 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]
53. Enhanced frequency of CFTR gene variants in couples who are candidates for assisted reproductive technology treatment.
Tomaiuolo R; Fausto M; Elce A; Strina I; Ranieri A; Amato F; Castaldo G; De Placido G; Alviggi C
Clin Chem Lab Med; 2011 Aug; 49(8):1289-1293. PubMed ID: 21679131
[TBL] [Abstract][Full Text] [Related]
54. [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]
55. 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]
56. 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]
57. Andrological findings in infertile men with two (biallelic) CFTR mutations: results of a multicentre study in Germany and Austria comprising 71 patients.
Rudnik-Schöneborn S; Messner M; Vockel M; Wirleitner B; Pinggera GM; Witsch-Baumgartner M; Murtinger M; Kliesch S; Swoboda M; Sänger N; Zschocke J; Tüttelmann F
Hum Reprod; 2021 Feb; 36(3):551-559. PubMed ID: 33374015
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Mutations in CFTR gene and clinical correlation in Argentine patients with congenital bilateral absence of the vas deferens.
Levy EM; Granados P; Rawe V; Olmedo SB; Luna MC; Cafferata E; Pivetta OH
Medicina (B Aires); 2004; 64(3):213-8. PubMed ID: 15239534
[TBL] [Abstract][Full Text] [Related]
60. Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.
Dayangaç D; Erdem H; Yilmaz E; Sahin A; Sohn C; Ozgüç M; Dörk T
Hum Reprod; 2004 May; 19(5):1094-100. PubMed ID: 15070876
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
