Cargando…
Association study of six SNPs in PRM1, PRM2 and TNP2 genes in iranian infertile men with idiopathic azoospermia
Background: Histones are replaced by protamines to condensate and package DNA into the sperm head during mammalian spermatogenesis. Protamine genes defects have been reported to cause sperm DNA damage and male infertility. Objective: In this study relationship among some protamines genes family SNPs...
Autores principales: | Siasi, Elham, Aleyasin, Ahmad, Mowla, Javad, Sahebkashaf, Hamid |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research and Clinical Center for Infertility
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165950/ https://www.ncbi.nlm.nih.gov/pubmed/25246894 |
Ejemplares similares
-
Analysis of PRM1 and PRM2 Polymorphisms in Iranian
Infertile Men with Idiopathic Teratozoospermia
por: Dehghanpour, Fatemeh, et al.
Publicado: (2019) -
Correlation of Single Nucleotide Polymorphisms of PRM1, PRM2, PYGO2, and DAZL Genes with Male Infertility in North West of Iran
por: Ghadirkhomi, Elham, et al.
Publicado: (2022) -
Evaluation of the association between polymorphisms of PRM1 and PRM2 and the risk of male infertility: a systematic review, meta-analysis, and meta-regression
por: Nemati, Houshang, et al.
Publicado: (2020) -
Building PRM in sub-Saharan Africa
por: Tannor, Abena Yeboaa, et al.
Publicado: (2022) -
Loss of Prm1 leads to defective chromatin protamination, impaired PRM2 processing, reduced sperm motility and subfertility in male mice
por: Merges, Gina Esther, et al.
Publicado: (2022)