Results 31 to 40 of about 4,087 (216)

Varicocelectomy versus antioxidants in infertile men with isolated teratozoospermia: A randomized controlled trial. [PDF]

open access: yesClin Exp Reprod Med
Objective To compare the outcomes of microscopic subinguinal varicocelectomy versus oral antioxidants in managing male infertility associated with isolated teratozoospermia.
Saber-Khalaf M   +6 more
europepmc   +2 more sources

A Comparative Cross-Platform Analysis to Identify Potential Biomarker Genes for Evaluation of Teratozoospermia and Azoospermia [PDF]

open access: yes, 2022
Male infertility is a global public health concern. Teratozoospermia is a qualitative anomaly of spermatozoa morphology, contributing significantly to male infertility, whereas azoospermia is the complete absence of spermatozoa in the ejaculate.
Sahu, Jagajjit   +25 more
core   +1 more source

Case Report: Balanced Reciprocal Translocation t (17; 22) (p11.2; q11.2) and 10q23.31 Microduplication in an Infertile Male Patient Suffering From Teratozoospermia

open access: yesFrontiers in Genetics, 2022
Two chromosomal abnormalities are described in an infertile man suffering from teratozoospermia: balanced reciprocal translocation t (17; 22) (p11.2; q11.2) and a microduplication in the region 10q23.31.
Shan Huang   +5 more
doaj   +1 more source

Dysregulated Kinase Expression in Teratozoospermia and Implications for Male Infertility: An Integrated Gene Expression Study. [PDF]

open access: yesJ Reprod Infertil
Background: Teratozoospermia, characterized by abnormal sperm morphology, is a major contributor to male infertility. Kinases, enzymes that catalyze the transfer of phosphate groups to proteins, are crucial regulators of cellular signaling pathways and ...
Mousavi SZ   +3 more
europepmc   +2 more sources

One potential biomarker for teratozoospermia identified by in-depth integrative analysis of multiple microarray data [PDF]

open access: yes, 2021
Teratozoospermia is a common category of male infertility and with the increase in clinical patients and the increasing sophistication of assisted reproductive technology, there is an urgent need for an accurate semen diagnostic biomarker to accomplish ...
Han, Baoquan   +7 more
core   +1 more source

Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome

open access: yesFrontiers in Cell and Developmental Biology, 2021
Acephalic spermatozoa syndrome is a rare type of teratozoospermia, but its pathogenesis is largely unknown. Here, we performed whole-exome sequencing for 34 patients with acephalic spermatozoa syndrome and identified pathogenic variants in the X-linked ...
Yanwei Sha   +10 more
doaj   +1 more source

Human teratozoospermia-related AGTPBP1 R791H mutation is associated with sperm head and tail defects in a CRISPR-engineered murine model. [PDF]

open access: yesJ Assist Reprod Genet
Infertility is a pervasive global health concern affecting millions of couples worldwide. Approximately 7% of the male population is infertile. Teratozoospermia, defined by > 96% abnormal sperm morphology, is a major cause of infertility often linked to ...
Wang YY   +7 more
europepmc   +2 more sources

European Academy of Andrology guideline Management of oligo-astheno-teratozoospermia [PDF]

open access: yes, 2018
Background: Oligo-astheno-teratozoospermia is frequently reported in men from infertile couples. Its etiology remains, in the majority of cases, unknown with a variety of factors to contribute to its pathogenesis.
Colpi, G M   +7 more
core   +5 more sources

miR-508-5p and mir-510-5p expressions and their relationships with spermatozoa motility and morphology [PDF]

open access: yesJournal of Shahrekord University of Medical Sciences, 2020
Background and aims:miRNAs have regulatory functions in developmental processes. The stages of spermatogenesis can also be affected by miRNAs. We tried to detect a relationship between the expression of miR-508-5p and miR-510-5p and male infertility. The
Tahere Hasheminiya   +3 more
doaj   +1 more source

Phenotype of autosomal dominant Alport syndrome with a likely pathogenic heterozygous variant in the COL4A3 gene (Gly366Arg) and incidental teratozoospermia: A case report. [PDF]

open access: yesAn Sist Sanit Navar
Autosomal dominant Alport syndrome (ADAS) is the least common form of Alport syndrome, the second most common monogenic cause of chronic kidney disease after autosomal dominant polycystic kidney disease.
Martín Moreno V   +5 more
europepmc   +2 more sources

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