Showing results (151-160 of 193) with videos related to

Sort By:
Pageof 20
Human Reproduction (Oxford, England)|April 21, 2016
Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injectionClémentine Wambergue, Raoudha Zouari, Selima Fourati Ben Mustapha, et al.
Human Molecular Genetics|January 2, 2016
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWPJessica Escoffier, Hoi Chang Lee, Sandra Yassine, et al.
Clinical Genetics|July 3, 2024
Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non-obstructive azoospermia in an Iranian familyAmir Amiri-Yekta, Sharanya Sen, Florence Hazane-Puch, et al.
Molecular Human Reproduction|December 10, 2016
Spermaurin, an La1-like peptide from the venom of the scorpion Scorpio maurus palmatus, improves sperm motility and fertilization in different mammalian speciesGuillaume Martinez, Jean-Pascal Hograindleur, Sébastien Voisin, et al.
American Journal of Physiology. Cell Physiology|April 3, 2020
The essential role of intraflagellar transport protein IFT81 in male mice spermiogenesis and fertilityWei Qu, Shuo Yuan, Chao Quan, et al.
Clinical Genetics|July 12, 2019
Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutationsZine-Eddine Kherraf, Caroline Cazin, Charles Coutton, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagellaMariem Ben Khelifa, Charles Coutton, Raoudha Zouari, et al.
International Journal of Molecular Sciences|February 11, 2023
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm FlagellaGuillaume Martinez, Anne-Laure Barbotin, Caroline Cazin, et al.
Clinical Genetics|September 18, 2018
Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restrictionGraciane Petre, Patrick Lorès, Hervé Sartelet, et al.
Human Reproduction (Oxford, England)|May 26, 2012
MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermiaCharles Coutton, Raoudha Zouari, Farid Abada, et al.
Pageof 20