Teratozoospermia: spotlight on the main genetic actors in the human

C Coutton, J Escoffier, G Martinez… - Human reproduction …, 2015 - academic.oup.com
BACKGROUND Male infertility affects> 20 million men worldwide and represents a major
health concern. Although multifactorial, male infertility has a strong genetic basis which has …

A Near‐Infrared Light‐Activated Photocage Based on a Ruthenium Complex for Cancer Phototherapy

G He, M He, R Wang, X Li, H Hu… - Angewandte Chemie …, 2023 - Wiley Online Library
Conventional photocages only respond to short wavelength light, which is a significant
obstacle to develo** efficient phototherapy in vivo. The development of photocages …

A mutation study of sperm head shape and motility in the mouse: lessons for the clinic

P De Boer, M De Vries, L Ramos - Andrology, 2015 - Wiley Online Library
Mouse mutants that show effects on sperm head shape, the sperm tail (flagellum), and
motility were analysed in a systematic way. This was achieved by grou** mutations in the …

Evidence for the involvement of proline-rich tyrosine kinase 2 in tyrosine phosphorylation downstream of protein kinase A activation during human sperm capacitation

MA Battistone, A Alvau, AM Salicioni… - Molecular human …, 2014 - academic.oup.com
Sperm capacitation involves an increase in intracellular Ca2+ concentration as well as in
protein kinase A (PKA)-dependent protein tyrosine (Tyr) phosphorylation. Interestingly, in …

Synaptotagmin‐4 promotes dendrite extension and melanogenesis in alpaca melanocytes by regulating Ca2+ influx via TRPM1 channels

Q Jia, S Hu, D Jiao, X Li, S Qi… - Cell biochemistry and …, 2020 - Wiley Online Library
Synaptotagmin‐4 (SYT4) is a membrane protein that regulates membrane traffic in neurons
in a calcium‐dependent or calcium‐independent manner. In melanocytes, the intracellular …

Biallelic mutations in KATNAL2 cause male infertility due to oligo‐astheno‐teratozoospermia

X Wei, W Liu, X Zhu, Y Li, X Zhang, J Chen… - Clinical …, 2021 - Wiley Online Library
Abstract Oligo‐astheno‐teratozoospermia (OAT) is a common cause of male infertility, and
most of idiopathic OAT patients are thought to be caused by genetic defects. Here, we …

Androgen receptor function links human sexual dimorphism to DNA methylation

O Ammerpohl, S Bens, M Appari, R Werner, B Korn… - PLoS …, 2013 - journals.plos.org
Sex differences are well known to be determinants of development, health and disease.
Epigenetic mechanisms are also known to differ between men and women through X …

TEX13B is essential for metabolic reprogramming during germ cell differentiation

U Kumar, DVS Sudhakar, N Kumar, A Moitra… - Human …, 2024 - academic.oup.com
STUDY QUESTION What is the functional significance of Tex13b in male germ cell
development and differentiation? SUMMARY ANSWER Tex13b regulates male germ cell …

NR5A1 mutations are not associated with male infertility in Indian men

DVS Sudhakar, S Nizamuddin, G Manisha… - Andrologia, 2018 - Wiley Online Library
NR 5A1 or steroidogenic factor 1 (SF 1) is an autosomal gene, which encodes a protein that
is a member of nuclear receptor family. NR 5A1 regulates the transcription of numerous …

Meiotic epigenetic factor PRDM9 impacts sperm quality of hybrid mice

F Kusari, O Mihola, JC Schimenti… - Reproduction, 2020 - rep.bioscientifica.com
Reduced fertility of male mouse hybrids relative to their parents, or hybrid sterility, is
governed by the hybrid sterility 1 (Hst1) locus. Rescue experiments with transgenes carrying …