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UnknownClosure versus medical therapy for preventing recurrent stroke in patients with patent foramen ovale and a history of cryptogenic stroke or transient ischemic attack.
Not available
S-EPMC7389291 | biostudies-literature
UnknownResin Glycosides with <i>α</i>-Glucosidase and Protein Tyrosine Phosphatase 1B Inhibitory Activities from the Seeds of <i>Cuscuta japonica</i>.
Not available
S-EPMC12562854 | biostudies-literature
UnknownEnterotypes in asthenospermia patients with obesity.
Not available
S-EPMC9550853 | biostudies-literature
UnknownLoss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans.
Not available
S-EPMC10362269 | biostudies-literature
ProteomicsPan-cancer and multi-omics analyses reveal the diagnostic and prognostic value of BAZ2B
The BAZ2B gene belongs to the bromodomain gene family. The proteins encoded by members of this gene family are important components of chromatin remodelling complexes and have a potential role in transcriptional activation. However, the biological significance of BAZ2B in pan-cancer is unknown. In t...
ORGANISM(S): Homo Sapiens 
2024-07-26 | PXD054319 |
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
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 |
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