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ProteomicsAged Mouse Muscle: Sedentary or Exercised Animals with or without Nicotinamide N-methyltransferase Inhibitor Treatment
Aged (22-mo) female mice (n=35), obtained from the US NIH National Institute on Aging (NIA) Aged Rodent Colony, were randomly assigned to one of four groups: saline-treated sedentary ( n=9), nicotinamide N-methyltransferase inhibitor (NNMTi)-treated sedentary (10 mg/kg body weight; n=9), saline-trea...
ORGANISM(S): Mus Musculus (ncbitaxon:10090) 
2024-05-07 | MSV000094700 | MassIVE
Unknown#COVIDisAirborne: AI-Enabled Multiscale Computational Microscopy of Delta SARS-CoV-2 in a Respiratory Aerosol.
Not available
S-EPMC8609898 | biostudies-literature
TranscriptomicsHDAC inhibition by TSA and Butyrate In Flt3L-elicited DC
Butyrate induces Treg via HDACi activity Microarray of DC treated with TSA or Butyrate over untreated
ORGANISM(S): Mus musculus 
2013-10-15 | E-GEOD-51263 | biostudies-arrayexpress
TranscriptomicsChanges in Mouse Uterine Lumenal Epithelial Cell Transcriptome in Estrus Compared to Proestrus
The potential for xenoestrogens and other environmental chemicals to alter female reproductive function calls for the study of their affects on endogenous hormone-regulated gene expression pathways during uterine tissue remodeling which occurs as part of the menstrual/estrus cycle. However, our know...
ORGANISM(S): Mus musculus 
2013-06-07 | E-GEOD-46813 | biostudies-arrayexpress
ProteomicsSystems pharmacology using mass spectrometry identifies critical response nodes in prostate cancer
Pelleted non-perturbed LNCaP cells were lysed using LysisBuffer (8 M urea, 0.1 M ammonium bicarbonate, 0.1 % RapiGest) and nucleic acids sheared using sonication.
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
2018-01-22 | MSV000081956 | MassIVE
UnknownRapid epitaxy-free graphene synthesis on silicidated polycrystalline platinum.
Not available
S-EPMC4518308 | biostudies-literature
TranscriptomicsRNA-seq of hepatocytes obtained through step-wise differentiation of hIPSCs from a patient with A1AT deficiency and its point mutation-corrected isogenic hIPSC line. Comparison to primary hepatocytes from a healthy donor and an A1AT-deficient patient.
A1AT deficiency is an autosomal not recessive disorder caused by mutations in the SERPINA1 gene. Individuals with the Z variant retain polymerised protein in the endoplasmic reticulum of hepatocytes, predisposing them to liver disease. This study primarily aimed to uncover the molecular mechanisms t...
ORGANISM(S): Homo sapiens 
2018-06-26 | E-MTAB-6781 | biostudies-arrayexpress
UnknownCabozantinib in patients with advanced prostate cancer: results of a phase II randomized discontinuation trial.
Not available
S-EPMC4110249 | biostudies-literature
UnknownPresumed small vessel disease, imaging and cognition markers in the Alzheimer's Disease Neuroimaging Initiative.
Not available
S-EPMC8514859 | biostudies-literature
UnknownAssociation of longitudinal white matter degeneration and cerebrospinal fluid biomarkers of neurodegeneration, inflammation and Alzheimer's disease in late-middle-aged adults.
Not available
S-EPMC5723250 | biostudies-literature
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