[HTML][HTML] Globozoospermia: a case report and systematic review of literature

A Crafa, RA Condorelli, S La Vignera… - The World Journal of …, 2023 - ncbi.nlm.nih.gov
Purpose Globozoospermia is a genetic syndrome characterized by the presence of round-
headed spermatozoa and infertility due to the inability of these spermatozoa to fertilize the …

Association of CATSPER1, SPATA16 and TEX11 genes polymorphism with idiopathic azoospermia and oligospermia risk in Iranian population

M Behvarz, SA Rahmani, E Siasi Torbati… - BMC Medical …, 2022 - Springer
Background Male infertility is a heterogeneous disease which can occur due to
spermatogenesis defects. The idiopathic azoospermia and oligospermia are the common …

Genetic Insights into Teratozoospermia: A Comprehensive Computational Study of UTR Variants in AURKC, SPATA16, and SUN5

MA Kyrgiafini, Z Mamuris - DNA, 2023 - mdpi.com
Teratozoospermia, a complex male fertility disorder affecting sperm morphology, has been
linked to AURKC, SPATA16, and SUN5 gene defects. However, the sheer volume of SNPs …

[PDF][PDF] Γονιδιωματική: μελέτη των αιτίων της αντρικής υπογονιμότητας

ΜΗ Μαρκαντώνη - 2022 - ir.lib.uth.gr
Περίληψη Η υπογονιμότητα πλήττει πλέον το 15% των ζευγαριών παγκοσμίως, με τον
ανδρικό παράγοντα να ευθύνεται για το 50% των περιπτώσεων. Η ανδρική υπογονιμότητα …

Investigation of GRTH gene single nucleotide polymorphism in association with male infertility in Iranian population

SH Kashani, ES Tarbiati, ZS Talari, P Pakzad - Meta Gene, 2018 - Elsevier
Introduction GRTH gene is located on chromosome 11q24 and consists of 14 exons. GRTH
codes for a protein product which is involved in testicular function and spermatogenesis. The …