ab14748 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab14748 は 215 報の論文で使用されています。

  • Gentric G  et al. PML-Regulated Mitochondrial Metabolism Enhances Chemosensitivity in Human Ovarian Cancers. Cell Metab 29:156-173.e10 (2019). PubMed: 30244973
  • Ferreira JCB  et al. A selective inhibitor of mitofusin 1-ßIIPKC association improves heart failure outcome in rats. Nat Commun 10:329 (2019). PubMed: 30659190
  • Yeshaw WM  et al. Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility. Elife 8:N/A (2019). PubMed: 30741634
  • Wang H  et al. ?-Tocotrienol inhibits oxidative phosphorylation and triggers apoptosis by inhibiting mitochondrial complex I subunit NDUFB8 and complex II subunit SDHB. Toxicology 417:42-53 (2019). PubMed: 30769052
  • Miranda Mendonça AP  et al. Highly aggressive behavior induced by social stress is associated to reduced cytochrome c oxidase activity in mice brain cortex. Neurochem Int 126:210-217 (2019). PubMed: 30922923
  • Spangenberg L  et al. Deep sequencing discovery of causal mtDNA mutations in a patient with unspecific neurological disease. Mitochondrion 46:337-344 (2019). PubMed: 30227252
  • Tufi R  et al. Comprehensive Genetic Characterization of Mitochondrial Ca2+ Uniporter Components Reveals Their Different Physiological Requirements In Vivo. Cell Rep 27:1541-1550.e5 (2019). PubMed: 31042479
  • Tseng CC  et al. Rhodoptilometrin, a Crinoid-Derived Anthraquinone, Induces Cell Regeneration by Promoting Wound Healing and Oxidative Phosphorylation in Human Gingival Fibroblast Cells. Mar Drugs 17:N/A (2019). PubMed: 30818790
  • Liu HW  et al. Exercise training upregulates SIRT1 to attenuate inflammation and metabolic dysfunction in kidney and liver of diabetic db/db mice. Nutr Metab (Lond) 16:22 (2019). PubMed: 30988688
  • Potes Y  et al. Overweight in the Elderly Induces a Switch in Energy Metabolism that Undermines Muscle Integrity. Aging Dis 10:217-230 (2019). PubMed: 31011474
  • García-Roche M  et al. Impaired hepatic mitochondrial function during early lactation in dairy cows: Association with protein lysine acetylation. PLoS One 14:e0213780 (2019). PubMed: 30870481
  • Jackson CB  et al. A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement. Hum Mol Genet 28:639-649 (2019). PubMed: 30358850
  • Pulman J  et al. Mutations in the MRPS28 gene encoding the small mitoribosomal subunit protein bS1m in a patient with intrauterine growth retardation, craniofacial dysmorphism and multisystemic involvement. Hum Mol Genet 28:1445-1462 (2019). PubMed: 30566640
  • Mohanraj K  et al. Inhibition of proteasome rescues a pathogenic variant of respiratory chain assembly factor COA7. EMBO Mol Med 11:N/A (2019). PubMed: 30885959
  • Tomar D  et al. Blockade of MCU-Mediated Ca2+ Uptake Perturbs Lipid Metabolism via PP4-Dependent AMPK Dephosphorylation. Cell Rep 26:3709-3725.e7 (2019). PubMed: 30917323
  • Agnew T  et al. A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways. Cell Rep 25:3315-3328.e6 (2018). PubMed: 30566859
  • Munro B  et al. Nucleoside supplementation modulates mitochondrial DNA copy number in the dguok-/- zebrafish. Hum Mol Genet N/A:N/A (2018). PubMed: 30428046
  • Wali JA  et al. Loss of BIM increases mitochondrial oxygen consumption and lipid oxidation, reduces adiposity and improves insulin sensitivity in mice. Cell Death Differ 25:217-225 (2018). PubMed: 29053141
  • Straub IR  et al. Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS. Hum Mol Genet 27:178-189 (2018). PubMed: 29121267
  • O'Rourke AR  et al. Impaired muscle relaxation and mitochondrial fission associated with genetic ablation of cytoplasmic actin isoforms. FEBS J 285:481-500 (2018). PubMed: 29265728
  • Saita S  et al. PARL partitions the lipid transfer protein STARD7 between the cytosol and mitochondria. EMBO J 37:N/A (2018). PubMed: 29301859
  • Chen XF  et al. Effect of puerarin in promoting fatty acid oxidation by increasing mitochondrial oxidative capacity and biogenesis in skeletal muscle in diabetic rats. Nutr Diabetes 8:1 (2018). PubMed: 29330446
  • Iuso A  et al. Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy. Am J Hum Genet 102:1018-1030 (2018). PubMed: 29754768
  • Zamponi E  et al. Nrf2 stabilization prevents critical oxidative damage in Down syndrome cells. Aging Cell 17:e12812 (2018). PubMed: 30028071
  • Cao K  et al. Quantitative Analysis of Seven New Prostate Cancer Biomarkers and the Potential Future of the 'Biomarker Laboratory'. Diagnostics (Basel) 8:N/A (2018). PubMed: 30060509
  • Song KH  et al. Mitochondrial reprogramming via ATP5H loss promotes multimodal cancer therapy resistance. J Clin Invest 128:4098-4114 (2018). PubMed: 30124467
  • Quintana-Cabrera R  et al. The cristae modulator Optic atrophy 1 requires mitochondrial ATP synthase oligomers to safeguard mitochondrial function. Nat Commun 9:3399 (2018). PubMed: 30143614
  • Du Y  et al. SIRT5 deacylates metabolism-related proteins and attenuates hepatic steatosis in ob/ob mice. EBioMedicine 36:347-357 (2018). PubMed: 30279144
  • Tsai PI  et al. PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista Junctions. Mol Cell 69:744-756.e6 (2018). PubMed: 29456190
  • Peralta S  et al. ATAD3 controls mitochondrial cristae structure in mouse muscle, influencing mtDNA replication and cholesterol levels. J Cell Sci 131:N/A (2018). PubMed: 29898916
  • Thompson K  et al. OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect. EMBO Mol Med 10:N/A (2018). PubMed: 30201738
  • Joshi A  et al. Biochemical characterization of the PHARC-associated serine hydrolase ABHD12 reveals its preference for very-long-chain lipids. J Biol Chem 293:16953-16963 (2018). PubMed: 30237167
  • Yardeni T  et al. High content image analysis reveals function of miR-124 upstream of Vimentin in regulating motor neuron mitochondria. Sci Rep 8:59 (2018). PubMed: 29311649
  • Agnew T  et al. MacroD1 Is a Promiscuous ADP-Ribosyl Hydrolase Localized to Mitochondria. Front Microbiol 9:20 (2018). PubMed: 29410655
  • Zhou C  et al. Oncogenic HSP60 regulates mitochondrial oxidative phosphorylation to support Erk1/2 activation during pancreatic cancer cell growth. Cell Death Dis 9:161 (2018). WB . PubMed: 29415987
  • Goldberg J  et al. The mitochondrial ATP synthase is a shared drug target for aging and dementia. Aging Cell 17:N/A (2018). WB ; Mouse . PubMed: 29316249
  • Lim SC  et al. Loss of the Mitochondrial Fatty Acid ß-Oxidation Protein Medium-Chain Acyl-Coenzyme A Dehydrogenase Disrupts Oxidative Phosphorylation Protein Complex Stability and Function. Sci Rep 8:153 (2018). WB ; Human . PubMed: 29317722
  • Marrone L  et al. Generation of iPSCs carrying a common LRRK2 risk allele for in vitro modeling of idiopathic Parkinson's disease. PLoS One 13:e0192497 (2018). PubMed: 29513666
  • Lee JJ  et al. Basal mitophagy is widespread in Drosophila but minimally affected by loss of Pink1 or parkin. J Cell Biol 217:1613-1622 (2018). PubMed: 29500189
  • Becker C  et al. CLPP deficiency protects against metabolic syndrome but hinders adaptive thermogenesis. EMBO Rep 19:N/A (2018). PubMed: 29588285
  • Krysciak K  et al. Adaptation of motor unit contractile properties in rat medial gastrocnemius to treadmill endurance training: Relationship to muscle mitochondrial biogenesis. PLoS One 13:e0195704 (2018). PubMed: 29672614
  • Lehmer C  et al. A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALS. EMBO Mol Med 10:N/A (2018). WB, ICC/IF . PubMed: 29789341
  • Pittala S  et al. Targeting Liver Cancer and Associated Pathologies in Mice with a Mitochondrial VDAC1-Based Peptide. Neoplasia 20:594-609 (2018). IHC-P ; Mouse . PubMed: 29747160
  • Lu Y  et al. Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge. Sci Rep 8:8251 (2018). PubMed: 29844467
  • Bezawork-Geleta A  et al. Alternative assembly of respiratory complex II connects energy stress to metabolic checkpoints. Nat Commun 9:2221 (2018). PubMed: 29880867
  • Ludtmann MHR  et al. a-synuclein oligomers interact with ATP synthase and open the permeability transition pore in Parkinson's disease. Nat Commun 9:2293 (2018). ICC/IF . PubMed: 29895861
  • Vagnoni A & Bullock SL A cAMP/PKA/Kinesin-1 Axis Promotes the Axonal Transport of Mitochondria in Aging Drosophila Neurons. Curr Biol 28:1265-1272.e4 (2018). WB ; Drosophila melanogaster . PubMed: 29606421
  • Chuaijit S  et al. Identification of a novel mitochondrial complex I assembly factor ACDH-12 in Caenorhabditis elegans. Mitochondrion N/A:N/A (2018). PubMed: 29540318
  • Pashkovskaia N  et al. Mitochondrial ROS direct the differentiation of murine pluripotent P19 cells. Stem Cell Res 30:180-191 (2018). PubMed: 29957443
  • Wang L  et al. Mitofusin 2 Regulates Axonal Transport of Calpastatin to Prevent Neuromuscular Synaptic Elimination in Skeletal Muscles. Cell Metab 28:400-414.e8 (2018). PubMed: 30017354
  • Collins CM  et al. ATP synthase F1 subunits recruited to centromeres by CENP-A are required for male meiosis. Nat Commun 9:2702 (2018). PubMed: 30006572
  • Seong E  et al. Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects. Ann Neurol 83:1075-1088 (2018). PubMed: 29604224
  • Lin G  et al. Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to a-Synuclein Gain. Cell Metab N/A:N/A (2018). PubMed: 29909971
  • Ding L  et al. Seipin regulates lipid homeostasis by ensuring calcium-dependent mitochondrial metabolism. EMBO J 37:N/A (2018). PubMed: 30049710
  • Kelly AC  et al. Adrenergic receptor stimulation suppresses oxidative metabolism in isolated rat islets and Min6 cells. Mol Cell Endocrinol 473:136-145 (2018). WB . PubMed: 29360563
  • Kucherenko MM & Shcherbata HR Stress-dependent miR-980 regulation of Rbfox1/A2bp1 promotes ribonucleoprotein granule formation and cell survival. Nat Commun 9:312 (2018). Drosophila melanogaster . PubMed: 29358748
  • Kauppila JHK  et al. Base-excision repair deficiency alone or combined with increased oxidative stress does not increase mtDNA point mutations in mice. Nucleic Acids Res N/A:N/A (2018). WB . PubMed: 29860357
  • Zagnoli-Vieira G  et al. Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23). Neurol Genet 4:e262 (2018). PubMed: 30109272
  • Turner N  et al. A selective inhibitor of ceramide synthase 1 reveals a novel role in fat metabolism. Nat Commun 9:3165 (2018). PubMed: 30131496
  • Shanmughapriya S  et al. FOXD1-dependent MICU1 expression regulates mitochondrial activity and cell differentiation. Nat Commun 9:3449 (2018). PubMed: 30158529
  • Lobo-Jarne T  et al. Human COX7A2L Regulates Complex III Biogenesis and Promotes Supercomplex Organization Remodeling without Affecting Mitochondrial Bioenergetics. Cell Rep 25:1786-1799.e4 (2018). PubMed: 30428348
  • Hermle T  et al. Modeling Monogenic Human Nephrotic Syndrome in the Drosophila Garland Cell Nephrocyte. J Am Soc Nephrol 28:1521-1533 (2017). PubMed: 27932481
  • Yoon WH  et al. Loss of Nardilysin, a Mitochondrial Co-chaperone for a-Ketoglutarate Dehydrogenase, Promotes mTORC1 Activation and Neurodegeneration. Neuron 93:115-131 (2017). PubMed: 28017472
  • Cuillerier A  et al. Loss of hepatic LRPPRC alters mitochondrial bioenergetics, regulation of permeability transition and trans-membrane ROS diffusion. Hum Mol Genet 26:3186-3201 (2017). PubMed: 28575497
  • Zhang C  et al. Incompatibility between mitochondrial and nuclear genomes during oogenesis results in ovarian failure and embryonic lethality. Development 144:2490-2503 (2017). PubMed: 28576772
  • Campos JC  et al. Exercise reestablishes autophagic flux and mitochondrial quality control in heart failure. Autophagy 13:1304-1317 (2017). PubMed: 28598232
  • Feichtinger RG  et al. Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies. Am J Hum Genet 101:525-538 (2017). PubMed: 28942965
  • Cracan V  et al. A genetically encoded tool for manipulation of NADP+/NADPH in living cells. Nat Chem Biol 13:1088-1095 (2017). WB . PubMed: 28805804
  • Binek A  et al. Proteomic footprint of myocardial ischemia/reperfusion injury: Longitudinal study of the at-risk and remote regions in the pig model. Sci Rep 7:12343 (2017). WB ; Pig . PubMed: 28955040
  • Song W  et al. Activin signaling mediates muscle-to-adipose communication in a mitochondria dysfunction-associated obesity model. Proc Natl Acad Sci U S A N/A:N/A (2017). PubMed: 28739899
  • Lin H  et al. Early VGLUT1-specific parallel fiber synaptic deficits and dysregulated cerebellar circuit in the KIKO mouse model of Friedreich ataxia. Dis Model Mech 10:1529-1538 (2017). PubMed: 29259026
  • Brüggemann M  et al. Systematic Analysis of the Expression of the Mitochondrial ATP Synthase (Complex V) Subunits in Clear Cell Renal Cell Carcinoma. Transl Oncol 10:661-668 (2017). WB ; Human . PubMed: 28672194
  • Greggio C  et al. Enhanced Respiratory Chain Supercomplex Formation in Response to Exercise in Human Skeletal Muscle. Cell Metab 25:301-311 (2017). WB ; Human . PubMed: 27916530
  • Shi G & McQuibban GA The Mitochondrial Rhomboid Protease PARL Is Regulated by PDK2 to Integrate Mitochondrial Quality Control and Metabolism. Cell Rep 18:1458-1472 (2017). PubMed: 28178523
  • Beutner G  et al. Cyclophilin D regulates the dynamic assembly of mitochondrial ATP synthase into synthasomes. Sci Rep 7:14488 (2017). PubMed: 29101324
  • Li C  et al. Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome. Nat Commun 8:1257 (2017). PubMed: 29097652
  • Liu Y  et al. Systematic proteome and proteostasis profiling in human Trisomy 21 fibroblast cells. Nat Commun 8:1212 (2017). PubMed: 29089484
  • Sha L  et al. Asymmetric Arginine Dimethylation Modulates Mitochondrial Energy Metabolism and Homeostasis in Caenorhabditis elegans. Mol Cell Biol 37:N/A (2017). PubMed: 27994012
  • Perks KL  et al. Adult-onset obesity is triggered by impaired mitochondrial gene expression. Sci Adv 3:e1700677 (2017). PubMed: 28835921
  • Cohen J  et al. Astrocyte Senescence and Metabolic Changes in Response to HIV Antiretroviral Therapy Drugs. Front Aging Neurosci 9:281 (2017). PubMed: 28900395
  • Shneyer BI  et al. ROS induced distribution of mitochondria to filopodia by Myo19 depends on a class specific tryptophan in the motor domain. Sci Rep 7:11577 (2017). PubMed: 28912530
  • Gonzalez KL  et al. Disparate peroxisome-related defects in Arabidopsis pex6 and pex26 mutants link peroxisomal retrotranslocation and oil body utilization. Plant J 92:110-128 (2017). PubMed: 28742939
  • Theisen BE  et al. Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy. Am J Med Genet A 173:2505-2510 (2017). PubMed: 28650581
  • Bick AG  et al. Cardiovascular homeostasis dependence on MICU2, a regulatory subunit of the mitochondrial calcium uniporter. Proc Natl Acad Sci U S A 114:E9096-E9104 (2017). WB ; Mouse . PubMed: 29073106
  • Boutant M  et al. Mfn2 is critical for brown adipose tissue thermogenic function. EMBO J 36:1543-1558 (2017). PubMed: 28348166
  • Patrinostro X  et al. Relative importance of ßcyto- and ?cyto-actin in primary mouse embryonic fibroblasts. Mol Biol Cell 28:771-782 (2017). PubMed: 28077619
  • Zhang T  et al. Fancd2 in vivo interaction network reveals a non-canonical role in mitochondrial function. Sci Rep 7:45626 (2017). PubMed: 28378742
  • Schatton D  et al. CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs. J Cell Biol 216:675-693 (2017). WB ; Mouse . PubMed: 28188211
  • Gómez-Serrano M  et al. Differential proteomic and oxidative profiles unveil dysfunctional protein import to adipocyte mitochondria in obesity-associated aging and diabetes. Redox Biol 11:415-428 (2017). WB ; Human . PubMed: 28064117
  • Jiang YF  et al. Electron tomographic analysis reveals ultrastructural features of mitochondrial cristae architecture which reflect energetic state and aging. Sci Rep 7:45474 (2017). WB . PubMed: 28358017
  • Antonicka H  et al. A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability. EMBO Rep 18:28-38 (2017). PubMed: 27974379
  • Gonzalez-Hurtado E  et al. Loss of macrophage fatty acid oxidation does not potentiate systemic metabolic dysfunction. Am J Physiol Endocrinol Metab 312:E381-E393 (2017). PubMed: 28223293
  • Sawyer EM  et al. Testis-specific ATP synthase peripheral stalk subunits required for tissue-specific mitochondrial morphogenesis in Drosophila. BMC Cell Biol 18:16 (2017). PubMed: 28335714
  • Maio N  et al. A Single Adaptable Cochaperone-Scaffold Complex Delivers Nascent Iron-Sulfur Clusters to Mammalian Respiratory Chain Complexes I-III. Cell Metab 25:945-953.e6 (2017). PubMed: 28380382
  • Heden TD  et al. Greater Oxidative Capacity in Primary Myotubes from Endurance-trained Women. Med Sci Sports Exerc 49:2151-2157 (2017). PubMed: 28617704
  • Chen JV  et al. A Splice Variant of Centrosomin Converts Mitochondria to Microtubule-Organizing Centers. Curr Biol 27:1928-1940.e6 (2017). PubMed: 28669756
  • Choi S  et al. Mitochondrial calcium uniporter in Drosophila transfers calcium between the endoplasmic reticulum and mitochondria in oxidative stress-induced cell death. J Biol Chem 292:14473-14485 (2017). PubMed: 28726639
  • Kayser EB  et al. Region-Specific Defects of Respiratory Capacities in the Ndufs4(KO) Mouse Brain. PLoS One 11:e0148219 (2016). WB . PubMed: 26824698
  • Thompson K  et al. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number. Am J Hum Genet 99:860-876 (2016). PubMed: 27693233
  • Liu D  et al. Activation of mTORC1 is essential for ß-adrenergic stimulation of adipose browning. J Clin Invest 126:1704-16 (2016). PubMed: 27018708
  • Aguilera-Gomez A  et al. In vivo vizualisation of mono-ADP-ribosylation by dPARP16 upon amino-acid starvation. Elife 5:N/A (2016). ICC/IF ; Drosophila melanogaster . PubMed: 27874829
  • Luo B  et al. ATP-Dependent Lon Protease Contributes to Helicobacter pylori-Induced Gastric Carcinogenesis. Neoplasia 18:242-52 (2016). PubMed: 27108387
  • Sen A & Cox RT Clueless is a conserved ribonucleoprotein that binds the ribosome at the mitochondrial outer membrane. Biol Open 5:195-203 (2016). IHC ; Drosophila melanogaster . PubMed: 26834020
  • De La Fuente S  et al. Strategic Positioning and Biased Activity of the Mitochondrial Calcium Uniporter in Cardiac Muscle. J Biol Chem 291:23343-23362 (2016). PubMed: 27637331
  • Li HB  et al. Mitochondrial Ribosomal Protein L10 Associates with Cyclin B1/Cdk1 Activity and Mitochondrial Function. DNA Cell Biol 35:680-690 (2016). Human . PubMed: 27726420
  • Guarani V  et al. QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease. Elife 5:N/A (2016). PubMed: 27623147
  • Yu H  et al. Capitalizing Resolving Power of Density Gradient Ultracentrifugation by Freezing and Precisely Slicing Centrifuged Solution: Enabling Identification of Complex Proteins from Mitochondria by Matrix Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry. J Anal Methods Chem 2016:8183656 (2016). WB ; Human . PubMed: 27668122
  • Ludtmann MH  et al. Monomeric Alpha-Synuclein Exerts a Physiological Role on Brain ATP Synthase. J Neurosci 36:10510-10521 (2016). WB ; Rat . PubMed: 27733604
  • Bowman CE  et al. Requirement for the Mitochondrial Pyruvate Carrier in Mammalian Development Revealed by a Hypomorphic Allelic Series. Mol Cell Biol 36:2089-104 (2016). WB ; Mouse . PubMed: 27215380
  • Helman A  et al. p16(Ink4a)-induced senescence of pancreatic beta cells enhances insulin secretion. Nat Med N/A:N/A (2016). IHC ; Human . PubMed: 26950362
  • Sakakibara I  et al. Six1 homeoprotein drives myofiber type IIA specialization in soleus muscle. Skelet Muscle 6:30 (2016). WB ; Mouse . PubMed: 27597886
  • Vedelek V  et al. Testis-Specific Bb8 Is Essential in the Development of Spermatid Mitochondria. PLoS One 11:e0161289 (2016). PubMed: 27529784
  • 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). ICC/IF . PubMed: 27545886
  • Seiferling D  et al. Loss of CLPP alleviates mitochondrial cardiomyopathy without affecting the mammalian UPRmt. EMBO Rep 17:953-64 (2016). PubMed: 27154400
  • Peyta L  et al. Reduced cardiolipin content decreases respiratory chain capacities and increases ATP synthesis yield in the human HepaRG cells. Biochim Biophys Acta 1857:443-53 (2016). PubMed: 26768115
  • Schubert C  et al. Reduction of apoptosis and preservation of mitochondrial integrity under ischemia/reperfusion injury is mediated by estrogen receptor ß. Biol Sex Differ 7:53 (2016). PubMed: 27688871
  • Wrobel L  et al. The presence of disulfide bonds reveals an evolutionarily conserved mechanism involved in mitochondrial protein translocase assembly. Sci Rep 6:27484 (2016). PubMed: 27265872
  • Ponnalagu D  et al. Data supporting characterization of CLIC1, CLIC4, CLIC5 and DmCLIC antibodies and localization of CLICs in endoplasmic reticulum of cardiomyocytes. Data Brief 7:1038-44 (2016). PubMed: 27104215
  • Xie C  et al. Neuroprotection by selective neuronal deletion of Atg7 in neonatal brain injury. Autophagy 12:410-23 (2016). WB . PubMed: 26727396
  • Oxenoid K  et al. Architecture of the mitochondrial calcium uniporter. Nature 533:269-73 (2016). PubMed: 27135929
  • Janer A  et al. SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome. EMBO Mol Med 8:1019-38 (2016). PubMed: 27390132
  • McDonnell MM  et al. The Early-Acting Peroxin PEX19 Is Redundantly Encoded, Farnesylated, and Essential for Viability in Arabidopsis thaliana. PLoS One 11:e0148335 (2016). PubMed: 26824478
  • Shneyer BI  et al. Myo19 is an outer mitochondrial membrane motor and effector of starvation-induced filopodia. J Cell Sci 129:543-56 (2016). PubMed: 26659663
  • Casey JP  et al. Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1? JIMD Rep 26:13-9 (2016). PubMed: 26238252
  • Lim SC  et al. Loss of mitochondrial DNA-encoded protein ND1 results in disruption of complex I biogenesis during early stages of assembly. FASEB J 30:2236-48 (2016). PubMed: 26929434
  • Burridge PW  et al. Human induced pluripotent stem cell-derived cardiomyocytes recapitulate the predilection of breast cancer patients to doxorubicin-induced cardiotoxicity. Nat Med 22:547-56 (2016). PubMed: 27089514
  • Hwang HJ  et al. Mitochondrial-targeted aryl hydrocarbon receptor and the impact of 2,3,7,8-tetrachlorodibenzo-p-dioxin on cellular respiration and the mitochondrial proteome. Toxicol Appl Pharmacol 304:121-32 (2016). PubMed: 27105554
  • Yang H  et al. Adipose-Specific Deficiency of Fumarate Hydratase in Mice Protects Against Obesity, Hepatic Steatosis, and Insulin Resistance. Diabetes 65:3396-3409 (2016). PubMed: 27554470
  • Kluckova K  et al. Ubiquinone-binding site mutagenesis reveals the role of mitochondrial complex II in cell death initiation. Cell Death Dis 6:e1749 (2015). WB . PubMed: 25950479
  • Cui XA  et al. mRNA encoding Sec61ß, a tail-anchored protein, is localized on the endoplasmic reticulum. J Cell Sci 128:3398-410 (2015). IF . PubMed: 26272916
  • Vertii A  et al. Centrosome-intrinsic mechanisms modulate centrosome integrity during fever. Mol Biol Cell 26:3451-63 (2015). PubMed: 26269579
  • Jahani-Asl A  et al. CDK5 phosphorylates DRP1 and drives mitochondrial defects in NMDA-induced neuronal death. Hum Mol Genet 24:4573-83 (2015). PubMed: 26002103
  • Sen A  et al. Clueless, a protein required for mitochondrial function, interacts with the PINK1-Parkin complex in Drosophila. Dis Model Mech 8:577-89 (2015). PubMed: 26035866
  • Nordby P  et al. Independent effects of endurance training and weight loss on peak fat oxidation in moderately overweight men: a randomized controlled trial. J Appl Physiol (1985) 118:803-10 (2015). PubMed: 25614598
  • Gogendeau D  et al. Aneuploidy causes premature differentiation of neural and intestinal stem cells. Nat Commun 6:8894 (2015). PubMed: 26573328
  • Zhu M  et al. Mask loss-of-function rescues mitochondrial impairment and muscle degeneration of Drosophila pink1 and parkin mutants. Hum Mol Genet 24:3272-85 (2015). PubMed: 25743185
  • Wang ZH  et al. Loss of a Clueless-dGRASP complex results in ER stress and blocks Integrin exit from the perinuclear endoplasmic reticulum in Drosophila larval muscle. Biol Open 4:636-48 (2015). ICC/IF ; Drosophila melanogaster . PubMed: 25862246
  • 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
  • Peng M  et al. Inhibiting cytosolic translation and autophagy improves health in mitochondrial disease. Hum Mol Genet 24:4829-47 (2015). WB . PubMed: 26041819
  • Cagin U  et al. Mitochondrial retrograde signaling regulates neuronal function. Proc Natl Acad Sci U S A 112:E6000-9 (2015). PubMed: 26489648
  • Alston CL  et al. A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. Hum Genet 134:869-79 (2015). PubMed: 26008905
  • Liao X  et al. Kruppel-like factor 4 is critical for transcriptional control of cardiac mitochondrial homeostasis. J Clin Invest 125:3461-76 (2015). PubMed: 26241060
  • Vincent G  et al. Changes in mitochondrial function and mitochondria associated protein expression in response to 2-weeks of high intensity interval training. Front Physiol 6:51 (2015). WB . PubMed: 25759671
  • Teixeira FK  et al. ATP synthase promotes germ cell differentiation independent of oxidative phosphorylation. Nat Cell Biol 17:689-96 (2015). PubMed: 25915123
  • Nordsborg NB  et al. Oxidative capacity and glycogen content increase more in arm than leg muscle in sedentary women after intense training. J Appl Physiol (1985) 119:116-23 (2015). PubMed: 26023221
  • Guarani V  et al. QIL1 is a novel mitochondrial protein required for MICOS complex stability and cristae morphology. Elife 4:N/A (2015). PubMed: 25997101
  • Kao YT & Bartel B Elevated growth temperature decreases levels of the PEX5 peroxisome-targeting signal receptor and ameliorates defects of Arabidopsis mutants with an impaired PEX4 ubiquitin-conjugating enzyme. BMC Plant Biol 15:224 (2015). WB . PubMed: 26377801
  • Kopajtich R  et al. Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy. Am J Hum Genet 95:708-20 (2014). PubMed: 25434004
  • Caro AA  et al. N-acetylcysteine inhibits the up-regulation of mitochondrial biogenesis genes in livers from rats fed ethanol chronically. Alcohol Clin Exp Res 38:2896-906 (2014). PubMed: 25581647
  • Vega-Naredo I  et al. Mitochondrial metabolism directs stemness and differentiation in P19 embryonal carcinoma stem cells. Cell Death Differ : (2014). PubMed: 24832466
  • Weng Z  et al. Green tea epigallocatechin gallate binds to and inhibits respiratory complexes in swelling but not normal rat hepatic mitochondria. Biochem Biophys Res Commun 443:1097-104 (2014). Rat . PubMed: 24384371
  • Scott I  et al. GCN5-like protein 1 (GCN5L1) controls mitochondrial content through coordinated regulation of mitochondrial biogenesis and mitophagy. J Biol Chem 289:2864-72 (2014). WB ; Mouse . PubMed: 24356961
  • Nilsson R  et al. Metabolic enzyme expression highlights a key role for MTHFD2 and the mitochondrial folate pathway in cancer. Nat Commun 5:3128 (2014). WB ; Human . PubMed: 24451681
  • Jannig PR  et al. Autophagy signaling in skeletal muscle of infarcted rats. PLoS One 9:e85820 (2014). WB ; Rat . PubMed: 24427319
  • Kuang C  et al. A novel fizzy/Cdc20-dependent mechanism suppresses necrosis in neural stem cells. Development 141:1453-64 (2014). Drosophila melanogaster . PubMed: 24598157
  • Khacho M  et al. Acidosis overrides oxygen deprivation to maintain mitochondrial function and cell survival. Nat Commun 5:3550 (2014). WB ; Mouse . PubMed: 24686499
  • Strittmatter L  et al. CLYBL is a polymorphic human enzyme with malate synthase and ß-methylmalate synthase activity. Hum Mol Genet 23:2313-23 (2014). PubMed: 24334609
  • Shiba-Fukushima K  et al. PINK1-mediated phosphorylation of Parkin boosts Parkin activity in Drosophila. PLoS Genet 10:e1004391 (2014). WB ; Drosophila melanogaster . PubMed: 24901221
  • Alavian KN  et al. An uncoupling channel within the c-subunit ring of the F1FO ATP synthase is the mitochondrial permeability transition pore. Proc Natl Acad Sci U S A 111:10580-5 (2014). WB ; Human . PubMed: 24979777
  • Li L  et al. Drosophila Syd-1, Liprin-a, and Protein Phosphatase 2A B' Subunit Wrd Function in a Linear Pathway to Prevent Ectopic Accumulation of Synaptic Materials in Distal Axons. J Neurosci 34:8474-87 (2014). Drosophila melanogaster . PubMed: 24948803
  • Yun J  et al. MUL1 acts in parallel to the PINK1/parkin pathway in regulating mitofusin and compensates for loss of PINK1/parkin. Elife (Cambridge) 3:e01958 (2014). ICC/IF ; Drosophila melanogaster . PubMed: 24898855
  • Ivatt RM  et al. Genome-wide RNAi screen identifies the Parkinson disease GWAS risk locus SREBF1 as a regulator of mitophagy. Proc Natl Acad Sci U S A 111:8494-9 (2014). ICC/IF ; Drosophila melanogaster . PubMed: 24912190
  • Charan RA  et al. Inhibition of apoptotic Bax translocation to the mitochondria is a central function of parkin. Cell Death Dis 5:e1313 (2014). PubMed: 24991765
  • Teh JT  et al. Isoprenylcysteine carboxylmethyltransferase regulates mitochondrial respiration and cancer cell metabolism. Oncogene 0:N/A (2014). PubMed: 25151967
  • Gao J  et al. CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins. J Cell Biol 207:213-23 (2014). PubMed: 25349259
  • 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). PubMed: 25293719
  • Kemppainen KK  et al. Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency. Hum Mol Genet 23:2078-93 (2014). IHC-P ; Drosophila melanogaster . PubMed: 24293544
  • Sood A  et al. A Mitofusin-2-dependent inactivating cleavage of Opa1 links changes in mitochondria cristae and ER contacts in the postprandial liver. Proc Natl Acad Sci U S A 111:16017-22 (2014). PubMed: 25352671
  • Pogson JH  et al. The complex I subunit NDUFA10 selectively rescues Drosophila pink1 mutants through a mechanism independent of mitophagy. PLoS Genet 10:e1004815 (2014). PubMed: 25412178
  • Baggio F  et al. Drosophila melanogaster LRPPRC2 is involved in coordination of mitochondrial translation. Nucleic Acids Res 42:13920-38 (2014). WB ; Drosophila melanogaster . PubMed: 25428350
  • Hegde VR  et al. Glia are critical for the neuropathology of complex I deficiency in Drosophila. Hum Mol Genet 23:4686-92 (2014). PubMed: 24760769
  • Houštek J  et al. Effects of mtDNA in SHR-mtF344 versus SHR conplastic strains on reduced OXPHOS enzyme levels, insulin resistance, cardiac hypertrophy, and systolic dysfunction. Physiol Genomics 46:671-8 (2014). PubMed: 25073601
  • Andersen TR  et al. A preliminary study: effects of football training on glucose control, body composition, and performance in men with type 2 diabetes. Scand J Med Sci Sports 24 Suppl 1:43-56 (2014). PubMed: 24903461
  • Jacobs RA  et al. Fast-Twitch Glycolytic Skeletal Muscle Is Predisposed to Age-Induced Impairments in Mitochondrial Function. J Gerontol A Biol Sci Med Sci : (2013). PubMed: 23371970
  • Jacobs RA  et al. The C57Bl/6 mouse serves as a suitable model of human skeletal muscle mitochondrial function. Exp Physiol 98:908-21 (2013). PubMed: 23180810
  • Riehle C  et al. Insulin receptor substrate signaling suppresses neonatal autophagy in the heart. J Clin Invest 123:5319-33 (2013). WB ; Mouse . PubMed: 24177427
  • Dolga AM  et al. Mitochondrial small conductance SK2 channels prevent glutamate-induced oxytosis and mitochondrial dysfunction. J Biol Chem 288:10792-804 (2013). WB ; Human . PubMed: 23430260
  • Haack TB  et al. ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy. Am J Hum Genet N/A:N/A (2013). WB ; Human . PubMed: 23849775
  • Chang TK  et al. Uba1 functions in Atg7- and Atg3-independent autophagy. Nat Cell Biol 15:1067-78 (2013). PubMed: 23873149
  • de Castro IP  et al. Drosophila ref(2)P is required for the parkin-mediated suppression of mitochondrial dysfunction in pink1 mutants. Cell Death Dis 4:e873 (2013). WB ; Drosophila melanogaster . PubMed: 24157867
  • Schlehe JS  et al. The mitochondrial disease associated protein Ndufaf2 is dispensable for Complex-1 assembly but critical for the regulation of oxidative stress. Neurobiol Dis 58:57-67 (2013). WB ; Human . PubMed: 23702311
  • Wirth M  et al. Mitochondrial SIRT4-type proteins in Caenorhabditis elegans and mammals interact with pyruvate carboxylase and other acetylated biotin-dependent carboxylases. Mitochondrion 13:705-20 (2013). WB . PubMed: 23438705
  • Xu W  et al. Cigarette smoking exposure alters pebp1 DNA methylation and protein profile involved in MAPK signaling pathway in mice testis. Biol Reprod 89:142 (2013). WB ; Mouse . PubMed: 24198121
  • Jin SM & Youle RJ The accumulation of misfolded proteins in the mitochondrial matrix is sensed by PINK1 to induce PARK2/Parkin-mediated mitophagy of polarized mitochondria. Autophagy 9:1750-7 (2013). WB . PubMed: 24149988
  • Choi J  et al. Metabolic interaction between cancer cells and stromal cells according to breast cancer molecular subtype. Breast Cancer Res 15:R78 (2013). PubMed: 24020991
  • Gorai T  et al. F1Fo-ATPase, F-type proton-translocating ATPase, at the plasma membrane is critical for efficient influenza virus budding. Proc Natl Acad Sci U S A 109:4615-20 (2012). PubMed: 22393008
  • Gilbert JS  et al. Placental and vascular adaptations to exercise training before and during pregnancy in the rat. Am J Physiol Regul Integr Comp Physiol 303:R520-6 (2012). PubMed: 22814667
  • 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
  • Celotto AM  et al. Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction. PLoS One 6:e25823 (2011). WB ; Drosophila melanogaster . PubMed: 21991365
  • Tappenden DM  et al. The aryl hydrocarbon receptor interacts with ATP5a1, a subunit of the ATP synthase complex, and modulates mitochondrial function. Toxicol Appl Pharmacol 254:299-310 (2011). PubMed: 21616089
  • 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
  • Khanna MR  et al. Towards a membrane proteome in Drosophila: a method for the isolation of plasma membrane. BMC Genomics 11:302 (2010). PubMed: 20462449
  • Escobar-Alvarez S  et al. Inhibition of human peptide deformylase disrupts mitochondrial function. Mol Cell Biol 30:5099-109 (2010). WB ; Human . PubMed: 20805355
  • Brys K  et al. Disruption of insulin signalling preserves bioenergetic competence of mitochondria in ageing Caenorhabditis elegans. BMC Biol 8:91 (2010). WB ; Caenorhabditis elegans . PubMed: 20584279
  • Ziviani E  et al. Drosophila parkin requires PINK1 for mitochondrial translocation and ubiquitinates mitofusin. Proc Natl Acad Sci U S A 107:5018-23 (2010). WB ; Drosophila melanogaster . PubMed: 20194754
  • Cox RT & Spradling AC Clueless, a conserved Drosophila gene required for mitochondrial subcellular localization, interacts genetically with parkin. Dis Model Mech 2:490-9 (2009). PubMed: 19638420
  • Yang JY  et al. Insulin stimulates Akt translocation to mitochondria: implications on dysregulation of mitochondrial oxidative phosphorylation in diabetic myocardium. J Mol Cell Cardiol 46:919-26 (2009). PubMed: 19249309
  • Liu K  et al. Functional analysis of FSP27 protein regions for lipid droplet localization, caspase-dependent apoptosis, and dimerization with CIDEA. Am J Physiol Endocrinol Metab 297:E1395-413 (2009). WB ; African green monkey . PubMed: 19843876
  • Wang N  et al. Comparative proteome profile of immature rat ovary during primordial follicle assembly and development. Proteomics 9:3425-34 (2009). PubMed: 19557761
  • Greiss S  et al. C. elegans SIR-2.1 translocation is linked to a proapoptotic pathway parallel to cep-1/p53 during DNA damage-induced apoptosis. Genes Dev 22:2831-42 (2008). PubMed: 18923081
  • Khidr L  et al. Role of SUV3 helicase in maintaining mitochondrial homeostasis in human cells. J Biol Chem 283:27064-73 (2008). PubMed: 18678873
  • Mast JD  et al. Reactive oxygen species act remotely to cause synapse loss in a Drosophila model of developmental mitochondrial encephalopathy. Development 135:2669-79 (2008). PubMed: 18599508
  • Yang J  et al. C-reactive protein augments hypoxia-induced apoptosis through mitochondrion-dependent pathway in cardiac myocytes. Mol Cell Biochem 310:215-26 (2008). PubMed: 18165866
  • Kim M  et al. Increased expression of the F(1)F(o) ATP synthase in response to iron in heart mitochondria. BMB Rep 41:153-7 (2008). PubMed: 18315952
  • Watanabe Y  et al. Adherent monomer-misfolded SOD1. PLoS One 3:e3497 (2008). PubMed: 18946506
  • Rea SL  et al. Relationship between mitochondrial electron transport chain dysfunction, development, and life extension in Caenorhabditis elegans. PLoS Biol 5:e259 (2007). PubMed: 17914900
  • Li Y  et al. An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria. J Biol Chem 282:17557-62 (2007). PubMed: 17452320
  • Park JS  et al. Yeast NDI1 improves oxidative phosphorylation capacity and increases protection against oxidative stress and cell death in cells carrying a Leber's hereditary optic neuropathy mutation. Biochim Biophys Acta 1772:533-42 (2007). PubMed: 17320357
  • Ventura N & Rea SL Caenorhabditis elegans mitochondrial mutants as an investigative tool to study human neurodegenerative diseases associated with mitochondrial dysfunction. Biotechnol J 2:584-95 (2007). PubMed: 17443764
  • Cortés-Hernández P  et al. ATP6 homoplasmic mutations inhibit and destabilize the human F1F0-ATP synthase without preventing enzyme assembly and oligomerization. J Biol Chem 282:1051-8 (2007). PubMed: 17121862
  • Stiburek L  et al. Knockdown of human Oxa1l impairs the biogenesis of F1Fo-ATP synthase and NADH:ubiquinone oxidoreductase. J Mol Biol 374:506-16 (2007). PubMed: 17936786
  • McQuibban GA  et al. Normal mitochondrial dynamics requires rhomboid-7 and affects Drosophila lifespan and neuronal function. Curr Biol 16:982-9 (2006). PubMed: 16713954
  • 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
  • Capaldi RA  et al. Immunological approaches to the characterization and diagnosis of mitochondrial disease. Mitochondrion 4:417-26 (2004). PubMed: 16120403
  • Kelly FD  et al. Toxoplasma gondii MAF1b Binds the Host Cell MIB Complex To Mediate Mitochondrial Association. mSphere 2:N/A (0). PubMed: 28567444

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

登録