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UnknownEnterotypes in asthenospermia patients with obesity.
Not available
S-EPMC9550853 | biostudies-literature
ProteomicsIdentification of ciliary protein interactome during senescence
Despite the importance of cellular senescence in human health, how damaged cells undergo senescence remains vague. We have previously shown that the translocation of a ciliary protein FBF1 to nucleus is essential for senescence induction in stressed cells. However, how dose FBF1 translocate from cil...
ORGANISM(S): Homo sapiens (Human) 
2024-08-19 | PXD045355 | Pride
Primary cilia Senescence 
UnknownGenetic landscape of human oocyte/embryo defects
Not available
S-EPMC12926087 | biostudies-literature
UnknownBi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest.
Not available
S-EPMC7332649 | biostudies-literature
ProteomicsRegulation of the PKD2 channel function and associated disease phenotypes by RASSF4
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common monogenic genetic disorders, caused by mutations in receptor PKD1 or ion channel PKD2, and is characterized by progressive renal cyst development with additional hepatic and extrarenal manifestations. As effective treatme...
ORGANISM(S): Homo Sapiens 
2026-02-13 | PXD074819 |
UnknownLarge-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects.
Not available
S-EPMC10080761 | biostudies-literature
UnknownLow-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese men.
Not available
S-EPMC4902876 | biostudies-literature
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