Screening of ΔF508 mutation and IVS8‐poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD
M Ghorbel, S Baklouti‐Gargouri, R Keskes… - Andrologia, 2012 - Wiley Online Library
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
[HTML][HTML] Screening of two neighboring CFTR mutations in Iranian infertile men with non-obstructive azoospermia
S Heidari, Z Hojati, M Motovali-Bashi - International Journal of …, 2017 - ncbi.nlm.nih.gov
The genetic association between cystic fibrosis transmembrane conductance regulator
(CFTR) gene mutations and male infertility due to congenital bilateral absence of vas …
(CFTR) gene mutations and male infertility due to congenital bilateral absence of vas …
Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure
High incidence of mutations in the cystic fibrosis transmembrane conductance regulator
(CFTR) gene is associated with congenital bilateral absence of the vas deferens (CBAVD) …
(CFTR) gene is associated with congenital bilateral absence of the vas deferens (CBAVD) …
[HTML][HTML] A survey of the common mutations and IVS8-Tn polymorphism of cystic fibrosis transmembrane conductance regulator gene in infertile men with …
F Asadi, R Mirfakhraie, F Mirzajani… - Iranian biomedical …, 2019 - ncbi.nlm.nih.gov
Background: Studies have revealed a strong association between mutations of CFTR gene
and the congenital bilateral absence of the vas deferens (CBAVD), but the role of this gene …
and the congenital bilateral absence of the vas deferens (CBAVD), but the role of this gene …
Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens
R Radpour, H Gourabi, MAS Gilani… - Molecular human …, 2006 - academic.oup.com
Congenital bilateral absence of the vas deferens (CBAVD) is a frequent cause of obstructive
azoospermia. Nearly 75% of men with CBAVD have at least one detectable common cystic …
azoospermia. Nearly 75% of men with CBAVD have at least one detectable common cystic …
The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques
K Safinejad, M Darbouy, SM Kalantar, S Zeinali… - Journal of assisted …, 2011 - Springer
Purpose To evaluate five common cystic fibrosis trans-membrane conductance regulator
(CFTR) mutations (ΔF508, G542X, R117H, W1282X and N1303K) in the Iranian infertile …
(CFTR) mutations (ΔF508, G542X, R117H, W1282X and N1303K) in the Iranian infertile …
Correlation Between CFTR Gene Mutations in Iranian Men With Congenital Absence of the Vas Deferens and Anatomical Genital Phenotype
R Radpour, H Gourabi, MAS Gilani… - Journal of …, 2008 - Wiley Online Library
Congenital bilateral absence of the vas deferens (CBAVD) and congenital unilateral
absence of the vas deferens (CUAVD) are 2 causes of male sterility; these phenotypes are …
absence of the vas deferens (CUAVD) are 2 causes of male sterility; these phenotypes are …
[HTML][HTML] The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens
WH Ni, L Jiang, QJ Fei, JY Jin, X Yang… - Asian journal of …, 2012 - ncbi.nlm.nih.gov
Congenital bilateral absence of the vas deferens (CBAVD) is a frequent cause of obstructive
azoospermia, and mutations of the cystic fibrosis transmembrane conductance regulator …
azoospermia, and mutations of the cystic fibrosis transmembrane conductance regulator …
Mutations in CFTR genes are associated with oligoasthenospermia in infertile men undergoing IVF
Q Li, Y Shen, LJ Zhao, JB Wang, X Huang - Andrologia, 2022 - Wiley Online Library
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation has been
clearly defined in congenital absence of the vas deferens (CAVD), which is an important …
clearly defined in congenital absence of the vas deferens (CAVD), which is an important …
The analysis of CFTR mutations in men with azoospermia, oligozoospermia and asthenozoospermia
R Ślęzak, M Szczepaniak, M Pasińska… - Ginekologia …, 2007 - journals.viamedica.pl
Mutations in cystic fibrosis transductance regulator gene (CFTR) are known to result in some
forms of male infertility. An association between CFTR gene mutations and obstructive …
forms of male infertility. An association between CFTR gene mutations and obstructive …