L'infertilité humaine représente un problème de santé publique qui affecte 10-15% des couples avec des causes masculines retrouvées dans 50% des cas. En raison de la grande diversité des anomalies responsables d'infertilité masculine nous avons choisi de
Ben Messaoud, Fatma
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ELAPOR1 is a copper-dependent tethering factor driving proacrosomal vesicle fusion during acrosome biogenesis. [PDF]
Shao T +7 more
europepmc +1 more source
Editorial: Fertilization and early development: genetics and epigenetics. [PDF]
Tian Y, Wang YF, Miao YL, Zhou LQ.
europepmc +1 more source
Homozygous mutation in spata16 is associated with male infertility in human globozoospermia
Globozoospermia is a rare (incidence
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Genetic Causes of Qualitative Sperm Defects: A Narrative Review of Clinical Evidence. [PDF]
Graziani A +6 more
europepmc +1 more source
Sperm-Derived Dysfunction of Human Embryos: Molecular Mechanisms and Clinical Resolution. [PDF]
Tesarik J, Mendoza Tesarik R.
europepmc +1 more source
Genetic etiological spectrum of sperm morphological abnormalities. [PDF]
Arora M +5 more
europepmc +1 more source
A rare variant of mixed total anomalous pulmonary venous connection with a garland configuration of the azygous system: Expanding the spectrum of anatomical variants. [PDF]
Siddharth CB +4 more
europepmc +1 more source
Function of manchette and intra-manchette transport in spermatogenesis and male fertility. [PDF]
Gao T, Liu Y, Li J, Zhang Y, Wu B.
europepmc +1 more source

