Before diagnosing stroke-like episodes in OPA1-related mitochondrial disorder, its imaging criteria must be met. [PDF]
Finsterer J.
europepmc +1 more source
FES‐derived MGE spheroids exhibit progenitor‐stage alterations in developmental trajectory and hypoxia‐responsive transcriptional programs, followed by functional disruption. Gestational hypoxia recapitulates impaired progenitor proliferation, shortened cell‐cycle progression, interneuron developmental abnormalities, and schizophrenia‐like behaviors in
Peiyan Ni +17 more
wiley +1 more source
Autosomal dominant <i>HK1</i>-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder. [PDF]
Ng BG +47 more
europepmc +1 more source
This work identifies acetylation‐dependent SDHA homeostasis as a determinant of tumor‐specific metabolic vulnerability. Guided by this mechanism, a modification‐selective inhibitor, ZPI‐3, selectively targets non‐acetylated SDHA, achieving tumor‐restricted SDH inhibition and effective bladder cancer control. Differential responses in clinical specimens
Kaikai Xu +9 more
wiley +1 more source
Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiency. [PDF]
Hedberg-Oldfors C +7 more
europepmc +1 more source
Susceptibility to COVID-19 in populations with health disparities: Posited involvement of mitochondrial disorder, socioeconomic stress, and pollutants. [PDF]
Yao Y, Lawrence DA.
europepmc +1 more source
IGF2BP1 promotes gemcitabine resistance in pancreatic cancer by stabilizing m6A‐modified FTH1 transcripts and protecting them in stress granules, thereby suppressing ferroptosis. Pharmacological inhibition of IGF2BP1 disrupts this protective pathway, restores ferroptotic sensitivity, and enhances gemcitabine efficacy in resistant tumors.
Ying‐Qin Zhu +10 more
wiley +1 more source
Mitochondrial Dysfunction in Attention Deficit Hyperactivity Disorder
Hakan Öğütlü +2 more
doaj +1 more source
Unraveling the molecular determinants of a rare human mitochondrial disorder caused by the P144L mutation of FDX2. [PDF]
Grifagni D +6 more
europepmc +1 more source
Camptocormia and Other Orthopedic Compromise Dominating Mitochondrial Disorder: A Case Report. [PDF]
Finsterer J, Chatterjee S, Ghosh R.
europepmc +1 more source

