[HTML][HTML] New single nucleotide polymorphism G5508A in the SEPT12 gene may be associated with idiopathic male infertility in Iranian men

M Shahhoseini, M Azad, M Sabbaghian… - Iranian Journal of …, 2015 - ncbi.nlm.nih.gov
Background: Male infertility is a multifactorial disorder, which affects approximately 10% of
couples at childbearing age with substantial clinical and social impact. Genetic factors are …

Association of single nucleotide polymorphism c.673C>A/p.Gln225Lys in SEPT12 gene with spermatogenesis failure in male idiopathic infertility in Northeast China

D Geng, X Yang, H Zhang, X Liu, Y Yu… - Journal of …, 2019 - journals.sagepub.com
Male infertility is a complex multifactorial disease affecting approximately 10% of couples
who want to have children. Some cases of infertility can be explained by genetic factors …

Single‐nucleotide polymorphism c.474G>A in the SEPT12 gene is a predisposing factor in male infertility

A Rafaee, A Mohseni Meybodi… - Molecular …, 2020 - Wiley Online Library
SEPT12 is a testis‐specific gene involved in the terminal differentiation of male germ cells.
SEPT12 protein is required for sperm head‐tail formation and acts as a fundamental …

[HTML][HTML] Comparative expression analysis of Septin 14 in testes of infertile men with normal spermatogenesis and spermatogenic failure

M Shafipour, M Sabbaghian… - Iranian Journal of …, 2014 - ncbi.nlm.nih.gov
Background: Septins are an evolutionary conserved group of GTP-binding and filament-
forming proteins that have diverse cellular roles. An increasing body of data implicates the …

SEPTIN12 Genetic Variants Confer Susceptibility to Teratozoospermia

YH Lin, YY Wang, HI Chen, YC Kuo, YW Chiou… - PLoS …, 2012 - journals.plos.org
It is estimated that 10–15% of couples are infertile and male factors account for about half of
these cases. With the advent of intracytoplasmic sperm injection (ICSI), many infertile men …

Expression and localization of Septin 14 gene and protein in infertile men testis

NV Barzi, K Kakavand, N Sodeifi, Z Ghezelayagh… - Reproductive …, 2020 - Elsevier
An increasing body of data implicates the Septin family in the pathology of several diseases,
including male fertility. The objective of this study was to evaluate the gene and protein …

Evaluation of SEPT2 and SEPT4 transcript contents in spermatozoa from men with asthenozoospermia and teratozoospermia

M Mazaheri Moghaddam… - Health Science …, 2021 - Wiley Online Library
Background and aims Motility and morphological defects of spermatozoa can cause male
infertility. Sperm RNAs are related to sperm quality. They are considered to have clinical …

Single‐Nucleotide Polymorphisms in the SEPTIN12 Gene May Be a Genetic Risk Factor for Japanese Patients With Sertoli Cell–Only Syndrome

H Miyakawa, T Miyamoto, E Koh… - Journal of …, 2012 - Wiley Online Library
Genetic mechanisms have been implicated as a cause of some cases of male infertility.
Recently, 10 novel genes involved in human spermatogenesis, including human SEPTIN12 …

The expression pattern of SEPT7 correlates with sperm morphology

HCA Chao, YH Lin, YC Kuo, CJ Shen, HA Pan… - Journal of assisted …, 2010 - Springer
Purpose To investigate the expression pattern of the SEPT7 protein during spermatogenesis
and its potential role in sperm function. Methods We first investigated the expression pattern …

Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men

T Miyamoto, A Tsujimura, Y Miyagawa, E Koh… - Journal of assisted …, 2012 - Springer
Purpose To investigate the association between SEPTIN12 gene variants and the risk of
azoospermia caused by meiotic arrest. Methods Mutational analysis of the SEPTIN12 gene …