Anti-NDUFB8抗体[20E9DH10C12] (ab110242)

发表研究结果有使用 ab110242?请让我们知道,以便我们可以引用本数据表中的参考文章。

ab110242 被引用在 45 文献中.

  • Pérez-Pérez R  et al. COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation. Cell Rep 16:2387-98 (2016). WB . PubMed: 27545886
  • Kauppila JH  et al. A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease. Cell Rep 16:2980-90 (2016). PubMed: 27626666
  • Gouspillou G  et al. Anthracycline-containing chemotherapy causes long-term impairment of mitochondrial respiration and increased reactive oxygen species release in skeletal muscle. Sci Rep 5:8717 (2015). WB ; Mouse . PubMed: 25732599
  • Oláhová M  et al. A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency. Eur J Hum Genet N/A:N/A (2014). WB ; Human . PubMed: 25293719
  • Gouspillou G  et al. Increased sensitivity to mitochondrial permeability transition and myonuclear translocation of endonuclease G in atrophied muscle of physically active older humans. FASEB J 28:1621-33 (2014). WB ; Human . PubMed: 24371120
  • Wedding IM  et al. Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions. PLoS One 9:e86340 (2014). IHC-Fr ; Human . PubMed: 24466038
  • 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
  • Hornig-Do HT  et al. Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations. EMBO Mol Med 6:183-93 (2014). WB ; Human . PubMed: 24413189
  • 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
  • Grünewald A  et al. Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue. J Neurosci Methods 232:143-9 (2014). IHC-Fr ; Human . PubMed: 24880043
  • 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
  • Pienaar IS  et al. Mitochondrial abnormality associates with type-specific neuronal loss and cell morphology changes in the pedunculopontine nucleus in Parkinson disease. Am J Pathol 183:1826-40 (2013). Human . PubMed: 24099985
  • Bruni F  et al. REXO2 is an oligoribonuclease active in human mitochondria. PLoS One 8:e64670 (2013). WB . PubMed: 23741365
  • Serre V  et al. Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency. Biochim Biophys Acta 1832:1304-12 (2013). Human . PubMed: 23603806
  • Almalki A  et al. Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency. Biochim Biophys Acta 1842:56-64 (2013). Human . PubMed: 24161539
  • Habersetzer J  et al. Human F1F0 ATP Synthase, Mitochondrial Ultrastructure and OXPHOS Impairment: A (Super-)Complex Matter? PLoS One 8:e75429 (2013). WB ; Human . PubMed: 24098383
  • Smith BK  et al. Submaximal ADP-stimulated respiration is impaired in ZDF rats and recovered by resveratrol. J Physiol 591:6089-101 (2013). PubMed: 24081154
  • Stiburek L  et al. YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation. Mol Biol Cell 23:1010-23 (2012). PubMed: 22262461
  • Fan W  et al. mtDNA lineage analysis of mouse L-cell lines reveals the accumulation of multiple mtDNA mutants and intermolecular recombination. Genes Dev 26:384-94 (2012). WB . PubMed: 22345519
  • 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
  • Thomas RR  et al. Recombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxin. Mitochondrion 11:108-18 (2011). PubMed: 20727424
  • Cameron JM  et al. Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes. Am J Hum Genet 89:486-95 (2011). WB ; Human . PubMed: 21944046
  • Tuppen HA  et al. The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families. Brain 133:2952-63 (2010). PubMed: 20819849
  • 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
  • Folbergrová J  et al. Sustained deficiency of mitochondrial complex I activity during long periods of survival after seizures induced in immature rats by homocysteic acid. Neurochem Int 56:394-403 (2010). PubMed: 19931336
  • Davis CW  et al. Nitration of the mitochondrial complex I subunit NDUFB8 elicits RIP1- and RIP3-mediated necrosis. Free Radic Biol Med 48:306-17 (2010). PubMed: 19897030
  • Dennerlein S  et al. Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit. Biochem J 430:551-8 (2010). PubMed: 20604745
  • 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
  • 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
  • Hangen E  et al. A brain-specific isoform of mitochondrial apoptosis-inducing factor: AIF2. Cell Death Differ 17:1155-66 (2010). PubMed: 20111043
  • Horvath R  et al. Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy. Brain 132:3165-74 (2009). PubMed: 19720722
  • Arthur CR  et al. Parkinson's disease brain mitochondria have impaired respirasome assembly, age-related increases in distribution of oxidative damage to mtDNA and no differences in heteroplasmic mtDNA mutation abundance. Mol Neurodegener 4:37 (2009). PubMed: 19775436
  • Iyer S  et al. Recombinant mitochondrial transcription factor A with N-terminal mitochondrial transduction domain increases respiration and mitochondrial gene expression. Mitochondrion 9:196-203 (2009). PubMed: 19460293
  • Son M  et al. Redox susceptibility of SOD1 mutants is associated with the differential response to CCS over-expression in vivo. Neurobiol Dis 34:155-62 (2009). PubMed: 19320055
  • Potluri P  et al. A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease. Mol Genet Metab 96:189-95 (2009). PubMed: 19185523
  • Nadanaciva S  et al. Lateral-flow immunoassay for detecting drug-induced inhibition of mitochondrial DNA replication and mtDNA-encoded protein synthesis. J Immunol Methods 343:1-12 (2009). PubMed: 19152798
  • Keeney PM  et al. Mitochondrial gene therapy augments mitochondrial physiology in a Parkinson's disease cell model. Hum Gene Ther 20:897-907 (2009). WB ; Human . PubMed: 19374590
  • Khidr L  et al. Role of SUV3 helicase in maintaining mitochondrial homeostasis in human cells. J Biol Chem 283:27064-73 (2008). PubMed: 18678873
  • Son M  et al. Isolated cytochrome c oxidase deficiency in G93A SOD1 mice overexpressing CCS protein. J Biol Chem 283:12267-75 (2008). PubMed: 18334481
  • Keeney PM  et al. Parkinson's disease brain mitochondrial complex I has oxidatively damaged subunits and is functionally impaired and misassembled. J Neurosci 26:5256-64 (2006). PubMed: 16687518
  • Wall JA  et al. Alterations in oxidative phosphorylation complex proteins in the hearts of transgenic mice that overexpress the p38 MAP kinase activator, MAP kinase kinase 6. Am J Physiol Heart Circ Physiol 291:H2462-72 (2006). WB ; Human, Mouse . PubMed: 16766635
  • Schilling B  et al. Rapid purification and mass spectrometric characterization of mitochondrial NADH dehydrogenase (Complex I) from rodent brain and a dopaminergic neuronal cell line. Mol Cell Proteomics 4:84-96 (2005). PubMed: 15591592
  • Schewe G [Organizational methods and possibilities of medical self-control]. MMW Munch Med Wochenschr 121:545-6 (1979). PubMed: 111043

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"