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UnknownDietary Composition, Meal Timing, and Cancer-Related Fatigue: Insights From the Women's Healthy Eating and Living Study.
Not available
S-EPMC11136880 | biostudies-literature
TranscriptomicsGene expression profiling in cardiac AngII-overexpressing mice (TG1306/1R)
Agonist-induced cardiac hypertrophy in TG1306/1R transgenic mice with cardiac angiotensin II overproduction leads to a gradual transition from a compensatory hypertrophic state to heart failure. To gain insight into the molecular mechanisms that play a role in maintaining cardiac integrity in the di...
ORGANISM(S): Mus musculus 
2010-05-18 | E-GEOD-13336 | biostudies-arrayexpress
UnknownCo-revolving topological defects in a nematic liquid crystal.
Not available
S-EPMC8573773 | biostudies-literature
UnknownFeasibility of Daily Assessments of Chemotherapy Toxicities to Predict Daily Exercise Behavior During a Home-Based Exercise Intervention.
Not available
S-EPMC12056855 | biostudies-literature
UnknownRhinosinusitis in an Australian mare caused by Flavodon flavus, a recently recognized invasive fungal pathogen of the horse.
Not available
S-EPMC7003237 | biostudies-literature
UnknownAtazanavir and Cardiovascular Risk Among Human Immunodeficiency Virus-Infected Patients: A Systematic Review.
Not available
S-EPMC5125135 | biostudies-literature
UnknownTransition from escaped to decomposed nematic defects, and vice versa.
Not available
S-EPMC8083252 | biostudies-literature
UnknownResults of a pivotal phase II study of brentuximab vedotin for patients with relapsed or refractory Hodgkin's lymphoma.
Not available
S-EPMC3646316 | biostudies-literature
ProteomicsMorpho-metabolic monitoring of individualized human cerebral organoid growth and quality in a non-destructive platform
DIA based proteomic analysis of 60 day Cerebral Brain Organoids
ORGANISM(S): Homo sapiens (Human) 
2026-05-28 | PXD076392 | Pride
Unguided brain organoids 
GenomicsTHAP11 mutations in a patient with a cblX-like phenotype implicates THAP11 in the regulation of cobalamin metabolism and early vertebrate development
Mutations in HCFC1 are associated with cblX (MIM309541), an X-linked recessive disorder, characterized by defects in cobalamin metabolism and other developmental defects. HCFC1 is a transcriptional co-regulator, which interacts with transcription factors to regulate the expression of a myriad of gen...
EGAS00001002201 | EGA
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