Results 211 to 220 of about 1,353,029 (249)

SIRT1/AMPK/PGC1α pathway in ischemic stroke: Elucidating neuroprotective strategies (Review). [PDF]

Mol Med Rep
Abbasi IN, Amin N, Xu Q, Hussain AB, Wu F, Yuan X, Yang Y, Ye S, Fang M, Jiang Y.   +9 more
europepmc   +1 more source

Spatial architecture of immunometabolism: Mitochondrial‑organelle interfaces in immune signaling (Review). [PDF]

Int J Mol Med
Wu Y, Yu H, Xia L, Yang L, Zhou Y, Yu Q.
europepmc   +1 more source

Adult-Onset Recessive Cerebellar Ataxia and Severe Multisystem Disease-Associated Genes: Hypomorphic Alleles and Clinical Interpretation Pitfalls. [PDF]

Genes (Basel)
Cipriano L, Petillo R, Priolo M, D'Ambrosio P.   +3 more
europepmc   +1 more source

Organelle regulation of ferroptosis after intracerebral hemorrhage. [PDF]

Redox Biol
Zhou N, Du Y, Wang Y, Zhao X, Ju Y.
europepmc   +1 more source

Stanniocalcin-1 Overexpression Protects Porcine Intestinal Epithelial Cells Against TBHP-Induced Oxidative Stress by Preserving Mitochondrial Homeostasis. [PDF]

Animals (Basel)
Wu L, Bin Y, Wei Y, Cui Z, Du J, Lv J, Xiang X.   +6 more
europepmc   +1 more source

The Molecular and Cellular Mechanisms of Melatonin: From Physiological Actions to Clinical Applications in Reproductive Medicine. [PDF]

Int J Mol Sci
Lee KI, Chen JH, Chen KH.
europepmc   +1 more source

PEX19 restricts porcine deltacoronavirus replication through farnesylation-dependent and -independent mechanisms. [PDF]

J Virol
Chen C, Su G, Wang Y, Xiong Y, Xiao W, Li Z, Fang L, Zhou Y, Xiao S.   +8 more
europepmc   +1 more source

Peroxisome biogenesis and peroxisome biogenesis disorders [PDF]

FEBS Letters, 2000
Peroxisome assembly in mammals requires more than 15 genes. Two isoforms of the peroxisome targeting signal type 1 (PTS1) receptor, Pex5pS and Pex5pL, are identified in mammals. Pex5pS and Pex5pL bind PTS1 proteins.
Yukio Fujiki
exaly   +5 more sources

Peroxisome Biogenesis Disorders [PDF]

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, 2006
Defects in PEX genes impair peroxisome assembly and multiple metabolic pathways confined to this organelle, thus providing the biochemical and molecular bases of the peroxisome biogenesis disorders (PBD). PBD are divided into two types—Zellweger syndrome
Yukio Fujiki
exaly   +4 more sources