The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in …

L Jafari, K Safinejad, M Nasiri, M Heidari… - Genes & Genomics, 2023 - Springer
Background Male infertility due to very severe oligozoospermia has been associated with
some genetic risk factors. Objective To investigate the distribution of the mutations in the …
被引用次数：2 相关文章 所有 4 个版本
[HTML] nih.gov

[HTML][HTML] The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia

L Jafari, K Safinejad, M Nasiri, M Heidari… - Journal of Medicine …, 2022 - ncbi.nlm.nih.gov
Due to progress in infertility etiology, several genetic bases of infertility are revealed today.
This study aimed to investigate the distribution of mutations in the CFTR gene, M470V …
被引用次数：4 相关文章 所有 10 个版本
[HTML] oup.com

Genetic risk factors in infertile men with severe oligozoospermia and azoospermia

GR Dohle, DJJ Halley, JO Van Hemel… - Human …, 2002 - academic.oup.com
BACKGROUND: Male infertility due to severe oligozoospermia and azoospermia has been
associated with a number of genetic risk factors. METHODS: In this study 150 men from …
被引用次数：458 相关文章 所有 13 个版本

Clinical and genetic evaluation in male infertility

S Racoviță, V Moshin, S Capcelea… - Revista de Ştiinţe ale …, 2022 - ibn.idsi.md
Background. Worldwide, it has been estimated that about 10–15% of couples attempting to
conceive are infertile, with male factors contributing to 50% of such cases. Genetic causes …
被引用次数：1 相关文章
[PDF] tubitak.gov.tr

Clinical and prognostic importance of chromosomal abnormalities, Y chromosome microdeletions, and CFTR gene mutations in individuals with azoospermia or …

Z Ocak, U Üyetürk, MM Dinçer - Turkish journal of medical …, 2014 - journals.tubitak.gov.tr
To illustrate the importance of genetic screening in the assessment of fertility and the correct
diagnosis in patients with azoospermia or severe oligospermia. Materials and methods: This …
被引用次数：20 相关文章 所有 8 个版本
[HTML] nih.gov

[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 …
被引用次数：11 相关文章 所有 14 个版本

Molecular analysis of defects in the CFTR gene and AZF locus of the Y chromosome in male infertility.

A Sobczyńska-Tomaszewska, D Bak… - The Journal of …, 2006 - europepmc.org
Objective To investigate the frequency and potential impact of mutations and polymorphisms
in the CFTR gene and deletions in AZF locus of the Y chromosome in patients with …
被引用次数：9 相关文章 所有 4 个版本

CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study

L Jiang, J Jin, S Wang, F Zhang, Y Dai, L Shi, S Zhang - Gene, 2017 - Elsevier
A variety of experimental studies have yielded evidence that the cystic fibrosis
transmembrane conductance regulator (CFTR) protein participates in the process of …
被引用次数：35 相关文章 所有 4 个版本

Clinical and genetic study in male infertility with azoospermia

S Racoviță, V Moshin, S Capcelea, A Mishina… - … în biomedicină și …, 2021 - ibn.idsi.md
Background. Worldwide, it has been estimated that about 7% of all men experience
infertility. About 20% of the causes of male infertility are of genetic etiology. The most …
被引用次数：2 相关文章 所有 4 个版本

Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia

J Kusić, D Radojković, V Maletić… - Srpski Arhiv za …, 2002 - europepmc.org
INTRODUCTION: Impaired infertility of the male partner is causative or contributOry to in up
to one half of all couples unable to conceive spontaneously. A considerable number of …
被引用次数：8 相关文章 所有 2 个版本