Quantitation and origin of the mitochondrial membrane potential in human cells lacking mitochondrial DNA.
about
Mammalian polynucleotide phosphorylase is an intermembrane space RNase that maintains mitochondrial homeostasisAlterations of the mitochondrial proteome caused by the absence of mitochondrial DNA: A proteomic viewGenome-wide RNAi screen identifies ATPase inhibitory factor 1 (ATPIF1) as essential for PARK2 recruitment and mitophagyRespiratory complex III is required to maintain complex I in mammalian mitochondriaLocalization of mitochondrial DNA base excision repair to an inner membrane-associated particulate fractionMitochondrion: A Promising Target for Nanoparticle-Based Vaccine Delivery Systems.Regulation of mitochondrial ATP synthase in cardiac pathophysiologyEffects of hydrogen peroxide on mitochondrial gene expression of intestinal epithelial cellsMetabolic adaptation to chronic inhibition of mitochondrial protein synthesis in acute myeloid leukemia cellsATPaseTb2, a unique membrane-bound FoF1-ATPase component, is essential in bloodstream and dyskinetoplastic trypanosomesCytochrome c oxidase is required for the assembly/stability of respiratory complex I in mouse fibroblastsImpaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivoMetformin inhibits mitochondrial complex I of cancer cells to reduce tumorigenesisInhibition of ATPIF1 ameliorates severe mitochondrial respiratory chain dysfunction in mammalian cells.DNA base excision repair activities and pathway function in mitochondrial and cellular lysates from cells lacking mitochondrial DNA.Parkin overexpression selects against a deleterious mtDNA mutation in heteroplasmic cybrid cellsFormation of an energized inner membrane in mitochondria with a gamma-deficient F1-ATPase.The other, forgotten genome: mitochondrial DNA and mental disorders.Syrosingopine sensitizes cancer cells to killing by metforminNeuronal and astrocyte dysfunction diverges from embryonic fibroblasts in the Ndufs4fky/fky mouse.The reductive hotspot hypothesis of mammalian aging: membrane metabolism magnifies mutant mitochondrial mischief.Apoptosis induced by persistent single-strand breaks in mitochondrial genome: critical role of EXOG (5'-EXO/endonuclease) in their repairThe awakening of an advanced malignant cancer: an insult to the mitochondrial genomeATP Depletion Via Mitochondrial F1F0 Complex by Lethal Factor is an Early Event in B. Anthracis-Induced Sudden Cell Death.Reduced Glucose Sensation Can Increase the Fitness of Saccharomyces cerevisiae Lacking Mitochondrial DNA.Impaired Cellular Bioenergetics Causes Mitochondrial Calcium Handling Defects in MT-ND5 Mutant Cybrids.The Mitochondrial Permeability Transition Pore: Channel Formation by F-ATP Synthase, Integration in Signal Transduction, and Role in Pathophysiology.Generating Rho-0 Cells Using Mesenchymal Stem Cell Lines.TCA Cycle and Mitochondrial Membrane Potential Are Necessary for Diverse Biological FunctionsHigh glucose uptake unexpectedly is accompanied by high levels of the mitochondrial ß-F1-ATPase subunit in head and neck squamous cell carcinoma.GRIM-19 is essential for maintenance of mitochondrial membrane potential.Mitochondrial transporters as novel targets for intracellular calcium signaling.Apoptosome-deficient cells lose cytochrome c through proteasomal degradation but survive by autophagy-dependent glycolysisPersistent damage induces mitochondrial DNA degradation.Mitochondrial consumption of cytosolic ATP: not so fast.Molecular Regulation of the Mitochondrial F(1)F(o)-ATPsynthase: Physiological and Pathological Significance of the Inhibitory Factor 1 (IF(1)).MtDNA depletion influences the transition of CD44 subtypes in human prostate cancer DU145 cells.A systematic assessment of mitochondrial function identified novel signatures for drug-induced mitochondrial disruption in cells.The novel phloroglucinol PMT7 kills glycolytic cancer cells by blocking autophagy and sensitizing to nutrient stress.Hypersensitivity of mtDNA-depleted cells to staurosporine-induced apoptosis: roles of Bcl-2 downregulation and cathepsin B.
P2860
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P2860
Quantitation and origin of the mitochondrial membrane potential in human cells lacking mitochondrial DNA.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Quantitation and origin of the ...... lls lacking mitochondrial DNA.
@en
Quantitation and origin of the ...... lls lacking mitochondrial DNA.
@nl
type
label
Quantitation and origin of the ...... lls lacking mitochondrial DNA.
@en
Quantitation and origin of the ...... lls lacking mitochondrial DNA.
@nl
prefLabel
Quantitation and origin of the ...... lls lacking mitochondrial DNA.
@en
Quantitation and origin of the ...... lls lacking mitochondrial DNA.
@nl
P2093
P2860
P1433
P1476
Quantitation and origin of the ...... ells lacking mitochondrial DNA
@en
P2093
M P Murphy
R D Appleby
W K Porteous
P2860
P304
P356
10.1046/J.1432-1327.1999.00350.X
P407
P50
P577
1999-05-01T00:00:00Z