Results 181 to 190 of about 44,980 (368)

Stress exposure in the mdx mouse model of Duchenne muscular dystrophy provokes a widespread metabolic response

open access: yesThe FEBS Journal, EarlyView.
A targeted mass spectrometry‐based metabolomics assay was conducted to identify the impact of stress exposure on the regulation of biological stress pathways in the mdx mouse model of Duchenne muscular dystrophy. We demonstrated a broad shift in the circulating stress‐relevant plasma metabolome associated with stressful scruff handling that was ...
Erynn E. Johnson, James M. Ervasti
wiley   +1 more source

THE COMPOSITION OF RAT LIVER XANTHINE OXIDASE AND ITS INHIBITION BY ANTABUSE

open access: hybrid, 1950
Dan A. Richert   +2 more
openalex   +1 more source

Xanthines Down-Regulate the Drug Transporter ABCG2 and Reverse Multidrug Resistance

open access: yesMolecular Pharmacology, 2012
Rui Ding, Jia Shi, Kirk Pabon, K. Scotto
semanticscholar   +1 more source

Stabilization of the catalytically active structure of a molybdenum‐dependent formate dehydrogenase depends on a highly conserved lysine residue

open access: yesThe FEBS Journal, EarlyView.
Molybdenum‐dependent formate dehydrogenases (Mo‐FDHs) contain a strictly conserved lysine residue (K44) in the vicinity of an electron‐transferring [4Fe‐4S] cluster and a catalytically active molybdenum atom coordinated by two molybdopterins (MPT‐1 and MPT‐2).
Feilong Li, Michael Lienemann
wiley   +1 more source

STIM2β is a Ca2+ signaling modulator for the regulation of mitotic clonal expansion and PPARG2 transcription in adipogenesis

open access: yesThe FEBS Journal, EarlyView.
STIM2β acts as the intracellular Ca2+ regulator during adipogenesis. By inhibiting intracellular Ca2+ levels and SOCE, STIM2β promotes mitotic clonal expansion in the early stage of adipogenesis. In the terminal differentiation stage, increased SOCE activity enhances PPARG2 gene transcription.
Su Ji Jeong   +3 more
wiley   +1 more source

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