Mutations in CFTR genes are associated with oligoasthenospermia in infertile men undergoing IVF

Genetics of the congenital absence of the vas deferens

(2020) Eric Bieth et al.   HUMAN GENETICS

Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD

(2020) Chengquan Ma et al.   Molecular Genetics & Genomic Medicine

Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles

(2019) P. Yuan et al.   Andrology

A systematic review and standardized clinical validity assessment of male infertility genes

(2019) Manon S Oud et al.   HUMAN REPRODUCTION

A novel mutation (−195C>A) in the promoter region of CFTR gene is associated with Chinese Congenital Bilateral Absence of Vas Deferens (CBAVD)

(2019) Jiarong Feng et al.   GENE

A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens

(2019) Bin Ge et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

The association between variants in the CFTR gene and nonobstructive male infertility: A meta‐analysis

(2019) Luchen Yang et al.   ANDROLOGIA

Semen quality of young adult ICSI offspring: the first results

(2016) F. Belva et al.   HUMAN REPRODUCTION

The Spectrum of CFTR Variants in Nonwhite Cystic Fibrosis Patients

(2016) Iris Schrijver et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens

(2015) Xiaojian Yang et al.   FERTILITY AND STERILITY

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

(2014) Shaoming Lu et al.   FERTILITY AND STERILITY

Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure

(2014) Himanshu Sharma et al.   GENE

Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia

(2013) Thassadite Dirami et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Cystic fibrosis transmembrane conductance regulator is correlated closely with sperm progressive motility and normal morphology in healthy and fertile men with normal sperm parameters

(2013) L.-Y. Jiang et al.   ANDROLOGIA

Regulation of male fertility by CFTR and implications in male infertility

(2012) Hui Chen et al.   HUMAN REPRODUCTION UPDATE

The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation

(2011) Baptiste Rode et al.   HUMAN MOLECULAR GENETICS

Defective CFTR-Dependent CREB Activation Results in Impaired Spermatogenesis and Azoospermia

(2011) Wen Ming Xu et al.   PLoS One

Cystic fibrosis transmembrane conductance regulator mutations in azoospermic and oligospermic men and their partners

(2009) Sabina Gallati et al.   REPRODUCTIVE BIOMEDICINE ONLINE