about
Physiological consequences of complex II inhibition for aging, disease, and the mKATP channelDevelopment of a new set of reference genes for normalization of real-time RT-PCR data of porcine backfat and longissimus dorsi muscle, and evaluation with PPARGC1A.Rapamycin increases mitochondrial efficiency by mtDNA-dependent reprogramming of mitochondrial metabolism in Drosophila.Use of fecal volatile organic compound analysis to discriminate between non-vaccinated and BCG-Vaccinated cattle prior to and after Mycobacterium bovis challenge.A metabolic model of the mitochondrion and its use in modelling diseases of the tricarboxylic acid cycle.High molecular weight forms of mammalian respiratory chain complex IIMassive Uterine Leiomyoma in a Patient with Friedreich's Ataxia: Is There a Possible Association?Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiencyTricarboxylic acid cycle dysfunction as a cause of human diseases and tumor formation.OXPHOS mutations and neurodegenerationFamiliar Papillary Thyroid Carcinoma in a Large Brazilian Family Is Not Associated with Succinate Dehydrogenase Defects.Inhibitors of succinate: quinone reductase/Complex II regulate production of mitochondrial reactive oxygen species and protect normal cells from ischemic damage but induce specific cancer cell death.Citric acid cycle and role of its intermediates in metabolism.Urinary metabolomic profiling in rats exposed to dietary di(2-ethylhexyl) phthalate (DEHP) using ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS).Regulation of succinate dehydrogenase activity by SIRT3 in mammalian mitochondria.Expression of Saccharomyces cerevisiae Sdh3p and Sdh4p paralogs results in catalytically active succinate dehydrogenase isoenzymes.Metabolic flexibility of mitochondrial respiratory chain disorders predicted by computer modelling.Measuring adriamycin-induced cardiac hemodynamic dysfunction with a proteomics approach.Identification of the flavoprotein of succinate dehydrogenase and aconitase as in vitro mitochondrial substrates of Fgr tyrosine kinase.Succinate <=> Fumarate (with FAD redox reaction on enzyme)Effects of site-directed mutations in Escherichia coli succinate dehydrogenase on the enzyme activity and production of superoxide radicals.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Succinate dehydrogenase deficiency in human
@ast
Succinate dehydrogenase deficiency in human
@en
Succinate dehydrogenase deficiency in human
@nl
type
label
Succinate dehydrogenase deficiency in human
@ast
Succinate dehydrogenase deficiency in human
@en
Succinate dehydrogenase deficiency in human
@nl
prefLabel
Succinate dehydrogenase deficiency in human
@ast
Succinate dehydrogenase deficiency in human
@en
Succinate dehydrogenase deficiency in human
@nl
P2093
P50
P3181
P1476
Succinate dehydrogenase deficiency in human
@en
P2093
A-P Gimenez
J-J Brière
V El Ghouzzi
P2888
P304
P3181
P356
10.1007/S00018-005-5237-6
P407
P577
2005-10-01T00:00:00Z