Cargando…
Structural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility
BACKGROUND: Impaired meiosis can result in absence of sperm in the seminal fluid. This condition, namely non-obstructive azoospermia (NOA), is one of the reasons of male infertility. Despite the low number of studies on meiosis 1-associated protein (M1AP) in the literature, M1AP is known to be cruci...
Autores principales: | Gerlevik, Umut, Ergoren, Mahmut Cerkez, Sezerman, Osman Uğur, Temel, Sehime Gulsun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944341/ https://www.ncbi.nlm.nih.gov/pubmed/35341049 http://dx.doi.org/10.7717/peerj.12947 |
Ejemplares similares
-
The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease
por: Temel, Şehime Gülsün, et al.
Publicado: (2019) -
Letter to the editor regarding the article “A case of hypertrophic and dilated cardiomyopathic sudden cardiac death: de novo mutation in TTN and SGCD genes”
por: Ergören, Mahmut Çerkez, et al.
Publicado: (2017) -
A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype
por: Tuncel, Gulten, et al.
Publicado: (2021) -
Lessons from Real Life Experience: Importance of In-House Sequencing and Smart Ratio-Based Real-Time PCR Outperform Multiplex Ligation-Dependent Probe Amplification in Prenatal Diagnosis for Spinal Muscular Atrophy: Bench to Bedside Diagnosis
por: Tuncel, Gulten, et al.
Publicado: (2023) -
CCR5-Δ32 gene variant frequency in the Turkish Cypriot population
por: Fahrioglu, Umut, et al.
Publicado: (2020)