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UnknownAkt2 kinase suppresses glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-mediated apoptosis in ovarian cancer cells via phosphorylating GAPDH at threonine 237 and decreasing its nuclear translocation.
Not available
S-EPMC3234938 | biostudies-literature
ProteomicsRobust Neurogenesis in Chronic Stroke Monkeys Following Mesenchymal Stem Cell Transplantation Plus Intermittent Theta-burst Stimulation
A significant population of chronic stroke patients urgently requires more effective therapies due to functional plateaus and limited intervention options. Intermittent theta-burst stimulation (iTBS) has been increasingly adopted in chronic-phase ischemic stroke management. However, the efficacy dec...
ORGANISM(S): Homo sapiens (Human) Macaca mulatta (Rhesus macaque) 
2026-03-12 | PXD071582 | Pride
Chronic stroke  nonhuman primate (nhps)  mesenchymal stem cells (mscs)  transplantation  intermittent theta-burst stimulation (itbs)  neuromodulation  neurogenesis 
UnknownBupleuri Radix Polysaccharides Alleviate MASLD by Regulating Muribaculaceae-Derived SCFAs in the Gut-Liver Axis.
Not available
S-EPMC12841138 | biostudies-literature
UnknownAn Anopheles stephensi Promoter-Trap: Augmenting Genome Annotation and Functional Genomics.
Not available
S-EPMC6169391 | biostudies-literature
UnknownProlonged administration of the granisetron transdermal delivery system reduces capecitabine plus oxaliplatin regimen induced nausea and vomiting.
Not available
S-EPMC11264757 | biostudies-literature
UnknownAnthropogenic intensification of Arctic anticyclonic circulation.
Not available
S-EPMC11864198 | biostudies-literature
UnknownBioinspired honeycomb-mimetic adaptive hyaluronic acid hydrogel composite scaffold: intelligent prevention and treatment of infection of bone implants and promotion of bone repair.
Not available
S-EPMC12664479 | biostudies-literature
TranscriptomicsRNA-seq of retinal organoids derived from RPGR patient-, control- and mutation-corrected-iPSC at different developmental stages
Retinitis pigmentosa (RP) is an irreversible and inherited retinopathy. RPGR mutations are the most common causes of this disease. It remains challenging to decipher the mechanism of RPGR mutation because of the lack of appropriate study models. The substitution of patient-specific diseased retina w...
ORGANISM(S): Homo sapiens 
2020-02-01 | E-MTAB-6490 | biostudies-arrayexpress
UnknownGenome-Wide Interaction Analysis With DASH Diet Score Identified Novel Loci for Systolic Blood Pressure.
Not available
S-EPMC10922535 | biostudies-literature
UnknownGenome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure.
Not available
S-EPMC10659476 | biostudies-literature
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