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ab110258 は 76 報の論文で使用されています。

  • Cowan DB  et al. Intracoronary Delivery of Mitochondria to the Ischemic Heart for Cardioprotection. PLoS One 11:e0160889 (2016). IHC-P ; Rabbit . PubMed: 27500955
  • Zoladz JA  et al. Endurance training increases the efficiency of rat skeletal muscle mitochondria. Pflugers Arch 468:1709-24 (2016). WB . PubMed: 27568192
  • Vargas JN  et al. Axonal localization and mitochondrial association of precursor microRNA 338. Cell Mol Life Sci 73:4327-4340 (2016). PubMed: 27229124
  • Ghosh A  et al. Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency. Hum Mol Genet N/A:N/A (2014). WB . PubMed: 24549041
  • Yamano K  et al. Mitochondrial Rab GAPs govern autophagosome biogenesis during mitophagy. Elife 3:e01612 (2014). WB ; Human . PubMed: 24569479
  • Hauser DN  et al. Post-translational decrease in respiratory chain proteins in the Polg mutator mouse brain. PLoS One 9:e94646 (2014). WB ; Mouse . PubMed: 24722488
  • Machova Urdzikova L  et al. Human multipotent mesenchymal stem cells improve healing after collagenase tendon injury in the rat. Biomed Eng Online 13:42 (2014). IHC-Fr ; Human . PubMed: 24712305
  • Sitarz KS  et al. Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblasts. Mol Genet Metab 112:57-63 (2014). WB ; Human . PubMed: 24725338
  • Kovács-Bogdán E  et al. Reconstitution of the mitochondrial calcium uniporter in yeast. Proc Natl Acad Sci U S A 111:8985-90 (2014). WB ; Human . PubMed: 24889638
  • Rice MW  et al. Assessment of cytochrome C oxidase dysfunction in the substantia nigra/ventral tegmental area in schizophrenia. PLoS One 9:e100054 (2014). WB ; Human . PubMed: 24941246
  • Yarham JW  et al. Defective i6A37 modification of mitochondrial and cytosolic tRNAs results from pathogenic mutations in TRIT1 and its substrate tRNA. PLoS Genet 10:e1004424 (2014). WB ; Human . PubMed: 24901367
  • Boczonadi V  et al. EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia. Nat Commun 5:4287 (2014). WB ; Human . PubMed: 24989451
  • Wanet A  et al. Mitochondrial remodeling in hepatic differentiation and dedifferentiation. Int J Biochem Cell Biol 54:174-85 (2014). PubMed: 25084555
  • Wilson WC  et al. A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression. Hum Mol Genet N/A:N/A (2014). WB ; Human . PubMed: 25008111
  • Lopez Sanchez MI  et al. Estrogen-mediated regulation of mitochondrial gene expression. Mol Endocrinol N/A:me20141077 (2014). PubMed: 25375021
  • van Bon BW  et al. CEP89 is required for mitochondrial metabolism and neuronal function in man and fly. Hum Mol Genet 22:3138-51 (2013). PubMed: 23575228
  • Samjoo IA  et al. Markers of skeletal muscle mitochondrial function and lipid accumulation are moderately associated with the homeostasis model assessment index of insulin resistance in obese men. PLoS One 8:e66322 (2013). WB ; Human . PubMed: 23776659
  • Stephenson EJ  et al. Skeletal muscle respiratory capacity is enhanced in rats consuming an obesogenic Western diet. Am J Physiol Endocrinol Metab 302:E1541-9 (2012). WB ; Rat . PubMed: 22496344
  • Little JP  et al. An acute bout of high-intensity interval training increases the nuclear abundance of PGC-1{alpha} and activates mitochondrial biogenesis in human skeletal muscle. Am J Physiol Regul Integr Comp Physiol 300:R1303-10 (2011). WB ; Human . PubMed: 21451146
  • Ferreira M  et al. Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1. Neurogenetics 12:9-17 (2011). PubMed: 21203893
  • Kemp JP  et al. Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency. Brain 134:183-95 (2011). PubMed: 21169334
  • Safdar A  et al. Aberrant mitochondrial homeostasis in the skeletal muscle of sedentary older adults. PLoS One 5:e10778 (2010). WB ; Human . PubMed: 20520725
  • Wydro M  et al. Targeting of the cytosolic poly(A) binding protein PABPC1 to mitochondria causes mitochondrial translation inhibition. Nucleic Acids Res 38:3732-42 (2010). PubMed: 20144953
  • Fogal V  et al. Mitochondrial p32 protein is a critical regulator of tumor metabolism via maintenance of oxidative phosphorylation. Mol Cell Biol 30:1303-18 (2010). PubMed: 20100866
  • Khalimonchuk O  et al. Formation of the redox cofactor centers during Cox1 maturation in yeast cytochrome oxidase. Mol Cell Biol 30:1004-17 (2010). PubMed: 19995914
  • Fogal V  et al. Mitochondrial p32 protein is a critical regulator of tumor metabolism via maintenance of oxidative phosphorylation. Mol Cell Biol 30:1303-18 (2010). PubMed: 20100866
  • Bestwick M  et al. The role of Coa2 in hemylation of yeast Cox1 revealed by its genetic interaction with Cox10. Mol Cell Biol 30:172-85 (2010). PubMed: 19841065
  • Leadsham JE & Gourlay CW cAMP/PKA signaling balances respiratory activity with mitochondria dependent apoptosis via transcriptional regulation. BMC Cell Biol 11:92 (2010). PubMed: 21108829
  • Gegg ME  et al. Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy. Hum Mol Genet 19:4861-70 (2010). PubMed: 20871098
  • Fassone E  et al. FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy. Hum Mol Genet 19:4837-47 (2010). PubMed: 20858599
  • Escobar-Alvarez S  et al. Inhibition of human peptide deformylase disrupts mitochondrial function. Mol Cell Biol 30:5099-109 (2010). WB ; Human . PubMed: 20805355
  • Nadanaciva S  et al. High-content screening for compounds that affect mtDNA-encoded protein levels in eukaryotic cells. J Biomol Screen 15:937-48 (2010). PubMed: 20625181
  • Koziel K  et al. Plasma membrane associated membranes (PAM) from Jurkat cells contain STIM1 protein is PAM involved in the capacitative calcium entry? Int J Biochem Cell Biol 41:2440-9 (2009). PubMed: 19622395
  • Bellance N  et al. Bioenergetics of lung tumors: alteration of mitochondrial biogenesis and respiratory capacity. Int J Biochem Cell Biol 41:2566-77 (2009). PubMed: 19712747
  • Horvath R  et al. Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy. Brain 132:3165-74 (2009). PubMed: 19720722
  • Rackham O  et al. Pentatricopeptide repeat domain protein 1 lowers the levels of mitochondrial leucine tRNAs in cells. Nucleic Acids Res 37:5859-67 (2009). PubMed: 19651879
  • Leshinsky-Silver E  et al. NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement. Mol Genet Metab 97:185-9 (2009). PubMed: 19364667
  • Crouser ED  et al. Monocyte activation by necrotic cells is promoted by mitochondrial proteins and formyl peptide receptors. Crit Care Med 37:2000-9 (2009). PubMed: 19384205
  • Villarroya J  et al. Altered gene transcription profiles in fibroblasts harboring either TK2 or DGUOK mutations indicate compensatory mechanisms. Exp Cell Res 315:1429-38 (2009). PubMed: 19265691
  • Gegg ME  et al. Silencing of PINK1 expression affects mitochondrial DNA and oxidative phosphorylation in dopaminergic cells. PLoS One 4:e4756 (2009). WB ; Human . PubMed: 19270741
  • Hakonen AH  et al. Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion. Hum Mol Genet 17:3822-35 (2008). PubMed: 18775955
  • Leroy C  et al. Protective effect of eicosapentaenoic acid on palmitate-induced apoptosis in neonatal cardiomyocytes. Biochim Biophys Acta 1781:685-93 (2008). PubMed: 18755291
  • Yeo WK  et al. Skeletal muscle adaptation and performance responses to once a day versus twice every second day endurance training regimens. J Appl Physiol 105:1462-70 (2008). PubMed: 18772325
  • Rorbach J  et al. The human mitochondrial ribosome recycling factor is essential for cell viability. Nucleic Acids Res 36:5787-99 (2008). PubMed: 18782833
  • Khidr L  et al. Role of SUV3 helicase in maintaining mitochondrial homeostasis in human cells. J Biol Chem 283:27064-73 (2008). PubMed: 18678873
  • Pierrel F  et al. Coa2 is an assembly factor for yeast cytochrome c oxidase biogenesis that facilitates the maturation of Cox1. Mol Cell Biol 28:4927-39 (2008). PubMed: 18541668
  • Fornuskova D  et al. The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues. Biochim Biophys Acta 1782:317-25 (2008). PubMed: 18319067
  • Balasubramanian S  et al. A novel histone deacetylase 8 (HDAC8)-specific inhibitor PCI-34051 induces apoptosis in T-cell lymphomas. Leukemia 22:1026-34 (2008). PubMed: 18256683
  • Caron M  et al. Contribution of mitochondrial dysfunction and oxidative stress to cellular premature senescence induced by antiretroviral thymidine analogues. Antivir Ther 13:27-38 (2008). PubMed: 18389896
  • Pagel-Langenickel I  et al. A discordance in rosiglitazone mediated insulin sensitization and skeletal muscle mitochondrial content/activity in Type 2 diabetes mellitus. Am J Physiol Heart Circ Physiol 293:H2659-66 (2007). PubMed: 17890427
  • Margineantu DH  et al. Hsp90 inhibition decreases mitochondrial protein turnover. PLoS One 2:e1066 (2007). PubMed: 17957250
  • Janssen GM  et al. The A3243G tRNALeu(UUR) mutation induces mitochondrial dysfunction and variable disease expression without dominant negative acting translational defects in complex IV subunits at UUR codons. Hum Mol Genet 16:2472-81 (2007). PubMed: 17656376
  • Ranney MK  et al. Multiple pathways regulating the anti-apoptotic protein clusterin in breast cancer. Biochim Biophys Acta 1772:1103-11 (2007). PubMed: 17689225
  • Ranney MK  et al. Multiple pathways regulating the anti-apoptotic protein clusterin in breast cancer. Biochim Biophys Acta 1772:1103-11 (2007). PubMed: 17689225
  • Pravenec M  et al. Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains. Genome Res 17:1319-26 (2007). PubMed: 17693571
  • Lebon S  et al. A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome. Mol Genet Metab 92:104-8 (2007). PubMed: 17604671
  • Fujita Y  et al. CHOP (C/EBP homologous protein) and ASNS (asparagine synthetase) induction in cybrid cells harboring MELAS and NARP mitochondrial DNA mutations. Mitochondrion 7:80-8 (2007). PubMed: 17276738
  • Gibala MJ  et al. Short-term sprint interval versus traditional endurance training: similar initial adaptations in human skeletal muscle and exercise performance. J Physiol 575:901-11 (2006). PubMed: 16825308
  • Pye D  et al. Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants. Nucleic Acids Res 34:e95 (2006). PubMed: 16885236
  • Mazzanti R  et al. Differential expression proteomics of human colon cancer. Am J Physiol Gastrointest Liver Physiol 290:G1329-38 (2006). PubMed: 16439467
  • Soucek K  et al. Transforming growth factor-beta1 inhibits all-trans retinoic acid-induced apoptosis. Leuk Res 30:607-23 (2006). PubMed: 16242776
  • Mazzanti R & Giulivi C Coordination of nuclear- and mitochondrial-DNA encoded proteins in cancer and normal colon tissues. Biochim Biophys Acta 1757:618-23 (2006). PubMed: 16730322
  • Clohessy JG  et al. Mcl-1 interacts with truncated Bid and inhibits its induction of cytochrome c release and its role in receptor-mediated apoptosis. J Biol Chem 281:5750-9 (2006). PubMed: 16380381
  • Schrauwen P  et al. Reduced skeletal muscle uncoupling protein-3 content in prediabetic subjects and type 2 diabetic patients: restoration by rosiglitazone treatment. J Clin Endocrinol Metab 91:1520-5 (2006). PubMed: 16384852
  • Stiburek L  et al. Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1. Biochem J 392:625-32 (2005). PubMed: 16083427
  • Stankiewicz AR  et al. Hsp70 inhibits heat-induced apoptosis upstream of mitochondria by preventing Bax translocation. J Biol Chem 280:38729-39 (2005). PubMed: 16172114
  • Sadacharan SK  et al. Localization of mitochondrial DNA encoded cytochrome c oxidase subunits I and II in rat pancreatic zymogen granules and pituitary growth hormone granules. Histochem Cell Biol 124:409-21 (2005). PubMed: 16133117
  • Jiang B  et al. Role of Smac/DIABLO in hydrogen peroxide-induced apoptosis in C2C12 myogenic cells. Free Radic Biol Med 39:658-67 (2005). PubMed: 16085184
  • Jiang B  et al. Heat shock pretreatment inhibited the release of Smac/DIABLO from mitochondria and apoptosis induced by hydrogen peroxide in cardiomyocytes and C2C12 myogenic cells. Cell Stress Chaperones 10:252-62 (2005). PubMed: 16184770
  • Rose P  et al. Beta-phenylethyl isothiocyanate mediated apoptosis; contribution of Bax and the mitochondrial death pathway. Int J Biochem Cell Biol 37:100-19 (2005). PubMed: 15381154
  • Miró O  et al. Upregulatory mechanisms compensate for mitochondrial DNA depletion in asymptomatic individuals receiving stavudine plus didanosine. J Acquir Immune Defic Syndr 37:1550-5 (2004). PubMed: 15577406
  • Gianni P  et al. Oxidative stress and the mitochondrial theory of aging in human skeletal muscle. Exp Gerontol 39:1391-400 (2004). PubMed: 15489062
  • Cisar CR  et al. Differential expression of mitochondrial electron transport chain proteins in cardiac tissues of broilers from pulmonary hypertension syndrome-resistant and -susceptible lines. Poult Sci 83:1420-6 (2004). PubMed: 15339019
  • Cheung NS  et al. Lactacystin-induced apoptosis of cultured mouse cortical neurons is associated with accumulation of PTEN in the detergent-resistant membrane fraction. Cell Mol Life Sci 61:1926-34 (2004). PubMed: 15289934
  • Guo Y  et al. Tim50, a component of the mitochondrial translocator, regulates mitochondrial integrity and cell death. J Biol Chem 279:24813-25 (2004). PubMed: 15044455
  • Chen JQ  et al. Mitochondrial localization of ERalpha and ERbeta in human MCF7 cells. Am J Physiol Endocrinol Metab 286:E1011-22 (2004). PubMed: 14736707

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