出版应用/物种/样本/稀释 | 参考文献 |
---|
| Sabbir M, Taylor C, Zahradka P. CAMKK2 regulates mitochondrial function by controlling succinate dehydrogenase expression, post-translational modification, megacomplex assembly, and activity in a cell-type-specific manner. Cell Commun Signal. 2021;19:98 pubmed 出版商
|
| Sato M, Kadomatsu T, Miyata K, Warren J, Tian Z, Zhu S, et al. The lncRNA Caren antagonizes heart failure by inactivating DNA damage response and activating mitochondrial biogenesis. Nat Commun. 2021;12:2529 pubmed 出版商
|
| Pereira R, Marti A, Olvera A, Tadinada S, Bjorkman S, Weatherford E, et al. OPA1 deletion in brown adipose tissue improves thermoregulation and systemic metabolism via FGF21. elife. 2021;10: pubmed 出版商
|
| Matlac D, Hadrava Vanova K, Bechmann N, Richter S, Folberth J, Ghayee H, et al. Succinate Mediates Tumorigenic Effects via Succinate Receptor 1: Potential for New Targeted Treatment Strategies in Succinate Dehydrogenase Deficient Paragangliomas. Front Endocrinol (Lausanne). 2021;12:589451 pubmed 出版商
|
- 免疫组化-石蜡切片; 人类; 1:100; 图 5o
| Schweizer L, Thierfelder F, Thomas C, Soschinski P, Suwala A, Stichel D, et al. Molecular characterization of CNS paragangliomas identifies cauda equina paragangliomas as a distinct tumor entity. Acta Neuropathol. 2020;140:893-906 pubmed 出版商
|
| Nowinski S, Solmonson A, Rusin S, Maschek J, Bensard C, Fogarty S, et al. Mitochondrial fatty acid synthesis coordinates oxidative metabolism in mammalian mitochondria. elife. 2020;9: pubmed 出版商
|
- 免疫印迹; 人类; 1:500-1:2000; 图 5c
| Wall C, Rose C, Adrian M, Zeng Y, Kirkpatrick D, Bingol B. PPEF2 Opposes PINK1-Mediated Mitochondrial Quality Control by Dephosphorylating Ubiquitin. Cell Rep. 2019;29:3280-3292.e7 pubmed 出版商
|
| Wyżewski Z, Gregorczyk Zboroch K, Mielcarska M, Bossowska Nowicka M, Struzik J, Szczepanowska J, et al. Mitochondrial Heat Shock Response Induced by Ectromelia Virus is Accompanied by Reduced Apoptotic Potential in Murine L929 Fibroblasts. Arch Immunol Ther Exp (Warsz). 2019;67:401-414 pubmed 出版商
|
- 免疫印迹; 人类; 图 1a
- 免疫印迹; 小鼠; 图 1b
| Maio N, Kim K, Holmes Hampton G, Singh A, Rouault T. Dimeric ferrochelatase bridges ABCB7 and ABCB10 homodimers in an architecturally defined molecular complex required for heme biosynthesis. Haematologica. 2019;: pubmed 出版商
|
| Signes A, Cerutti R, Dickson A, Benincá C, Hinchy E, Ghezzi D, et al. APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROS. EMBO Mol Med. 2019;11: pubmed 出版商
|
| Caino M, Seo J, Wang Y, Rivadeneira D, Gabrilovich D, Kim E, et al. Syntaphilin controls a mitochondrial rheostat for proliferation-motility decisions in cancer. J Clin Invest. 2017;127:3755-3769 pubmed 出版商
|
| Kitazawa S, Ebara S, Ando A, Baba Y, Satomi Y, Soga T, et al. Succinate dehydrogenase B-deficient cancer cells are highly sensitive to bromodomain and extra-terminal inhibitors. Oncotarget. 2017;8:28922-28938 pubmed 出版商
|
| Dadson K, Hauck L, Hao Z, Grothe D, Rao V, Mak T, et al. The E3 ligase Mule protects the heart against oxidative stress and mitochondrial dysfunction through Myc-dependent inactivation of Pgc-1α and Pink1. Sci Rep. 2017;7:41490 pubmed 出版商
|
| Rohlenova K, Sachaphibulkij K, Stursa J, Bezawork Geleta A, Blecha J, Endaya B, et al. Selective Disruption of Respiratory Supercomplexes as a New Strategy to Suppress Her2high Breast Cancer. Antioxid Redox Signal. 2017;26:84-103 pubmed 出版商
|
| Lopez Cruzan M, Sharma R, Tiwari M, Karbach S, Holstein D, Martin C, et al. Caspase-2 resides in the mitochondria and mediates apoptosis directly from the mitochondrial compartment. Cell Death Discov. 2016;2: pubmed
|
| Xie C, Ginet V, Sun Y, Koike M, Zhou K, Li T, et al. Neuroprotection by selective neuronal deletion of Atg7 in neonatal brain injury. Autophagy. 2016;12:410-23 pubmed 出版商
|
| Her Y, Nelson Holte M, MAHER L. Oxygen concentration controls epigenetic effects in models of familial paraganglioma. PLoS ONE. 2015;10:e0127471 pubmed 出版商
|
| Gouspillou G, Scheede Bergdahl C, Spendiff S, Vuda M, Meehan B, Mlynarski H, et al. Anthracycline-containing chemotherapy causes long-term impairment of mitochondrial respiration and increased reactive oxygen species release in skeletal muscle. Sci Rep. 2015;5:8717 pubmed 出版商
|
| Brobeil A, Viard M, Petri M, Steger K, Tag C, Wimmer M. Memory and PTPIP51--a new protein in hippocampus and cerebellum. Mol Cell Neurosci. 2015;64:61-73 pubmed 出版商
|
| Sverdlov A, Elezaby A, Behring J, Bachschmid M, Luptak I, Tu V, et al. High fat, high sucrose diet causes cardiac mitochondrial dysfunction due in part to oxidative post-translational modification of mitochondrial complex II. J Mol Cell Cardiol. 2015;78:165-73 pubmed 出版商
|
| Gill A, Hes O, Papathomas T, Å edivcová M, Tan P, Agaimy A, et al. Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients. Am J Surg Pathol. 2014;38:1588-602 pubmed 出版商
|
| Andersen T, Schmidt J, Thomassen M, Hornstrup T, Frandsen U, Randers M, 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. 2014;24 Suppl 1:43-56 pubmed 出版商
|
| Gill A, Toon C, Clarkson A, Sioson L, Chou A, Winship I, et al. Succinate dehydrogenase deficiency is rare in pituitary adenomas. Am J Surg Pathol. 2014;38:560-6 pubmed 出版商
|
| Gouspillou G, Sgarioto N, Kapchinsky S, Purves Smith F, Norris B, Pion C, et al. Increased sensitivity to mitochondrial permeability transition and myonuclear translocation of endonuclease G in atrophied muscle of physically active older humans. FASEB J. 2014;28:1621-33 pubmed 出版商
|
| Kovarova N, Mracek T, Nůsková H, Holzerová E, Vrbacky M, Pecina P, et al. High molecular weight forms of mammalian respiratory chain complex II. PLoS ONE. 2013;8:e71869 pubmed 出版商
|
| Cama A, Verginelli F, Lotti L, Napolitano F, Morgano A, D Orazio A, et al. Integrative genetic, epigenetic and pathological analysis of paraganglioma reveals complex dysregulation of NOTCH signaling. Acta Neuropathol. 2013;126:575-94 pubmed 出版商
|
| Lee P, Yau D, Lau P, Chan J. Plexiform fibromyxoma (plexiform angiomyxoid myofibroblastic tumor) of stomach: an unusual presentation as a fistulating abscess. Int J Surg Pathol. 2014;22:286-90 pubmed 出版商
|
| van Wietmarschen N, Moradian A, Morin G, Lansdorp P, Uringa E. The mammalian proteins MMS19, MIP18, and ANT2 are involved in cytoplasmic iron-sulfur cluster protein assembly. J Biol Chem. 2012;287:43351-8 pubmed 出版商
|
| Pavlov V, Kalinin D, Lukyanova E, Golovyuk A, Fedorova M, Pudova E, et al. Multiple paragangliomas: a case report. BMC Med Genomics. 2020;13:125 pubmed 出版商
|
| Ye H, Qin S, Li N, Lin M, Xu Y, Li X. A Rare Partner of TFE3 in the Xp11 Translocation Renal Cell Carcinoma: Clinicopathological Analyses and Detection of MED15-TFE3 Fusion. Biomed Res Int. 2019;2019:5974089 pubmed 出版商
|
| Arribat Y, Grepper D, Lagarrigue S, Richard J, Gachet M, Gut P, et al. Mitochondria in Embryogenesis: An Organellogenesis Perspective. Front Cell Dev Biol. 2019;7:282 pubmed 出版商
|
| Rojas Morales P, Tapia E, León Contreras J, González Reyes S, Jiménez Osorio A, Trujillo J, et al. Mechanisms of Fasting-Mediated Protection against Renal Injury and Fibrosis Development after Ischemic Acute Kidney Injury. Biomolecules. 2019;9: pubmed 出版商
|
| Puleston D, Buck M, Klein Geltink R, Kyle R, Caputa G, O Sullivan D, et al. Polyamines and eIF5A Hypusination Modulate Mitochondrial Respiration and Macrophage Activation. Cell Metab. 2019;: pubmed 出版商
|
| Ugarte Camara M, Fernandez Prado R, Lorda I, Rossello G, Gonzalez Enguita C, Cannata Ortiz P, et al. Positive/retained SDHB immunostaining in renal cell carcinomas associated to germline SDHB-deficiency: case report. Diagn Pathol. 2019;14:42 pubmed 出版商
|
| Bajzikova M, Kovarova J, Coelho A, Boukalova S, Oh S, Rohlenova K, et al. Reactivation of Dihydroorotate Dehydrogenase-Driven Pyrimidine Biosynthesis Restores Tumor Growth of Respiration-Deficient Cancer Cells. Cell Metab. 2019;29:399-416.e10 pubmed 出版商
|
| Atzmon A, Herrero M, Sharet Eshed R, Gilad Y, Senderowitz H, Elroy Stein O. Drug Screening Identifies Sigma-1-Receptor as a Target for the Therapy of VWM Leukodystrophy. Front Mol Neurosci. 2018;11:336 pubmed 出版商
|
| Zagnoli Vieira G, Bruni F, Thompson K, He L, Walker S, de Brouwer A, et al. Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23). Neurol Genet. 2018;4:e262 pubmed 出版商
|
| Kuang Y, Han X, Xu M, Yang Q. Oxaloacetate induces apoptosis in HepG2 cells via inhibition of glycolysis. Cancer Med. 2018;7:1416-1429 pubmed 出版商
|
| Pareek G, Thomas R, Pallanck L. Loss of the Drosophila m-AAA mitochondrial protease paraplegin results in mitochondrial dysfunction, shortened lifespan, and neuronal and muscular degeneration. Cell Death Dis. 2018;9:304 pubmed 出版商
|
| Kelly A, Camacho L, Pendarvis K, Davenport H, Steffens N, Smith K, et al. Adrenergic receptor stimulation suppresses oxidative metabolism in isolated rat islets and Min6 cells. Mol Cell Endocrinol. 2018;473:136-145 pubmed 出版商
|
| Feichtinger R, Oláhová M, Kishita Y, Garone C, Kremer L, Yagi M, et al. Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies. Am J Hum Genet. 2017;101:525-538 pubmed 出版商
|
| Naseri N, Bonica J, Xu H, Park L, Arjomand J, Chen Z, et al. Novel Metabolic Abnormalities in the Tricarboxylic Acid Cycle in Peripheral Cells From Huntington's Disease Patients. PLoS ONE. 2016;11:e0160384 pubmed 出版商
|
| Sverdlov A, Elezaby A, Qin F, Behring J, Luptak I, Calamaras T, et al. Mitochondrial Reactive Oxygen Species Mediate Cardiac Structural, Functional, and Mitochondrial Consequences of Diet-Induced Metabolic Heart Disease. J Am Heart Assoc. 2016;5: pubmed 出版商
|
| Hiniker A, Wong L, Berven S, Truong C, Adesina A, Margeta M. Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis. Acta Neuropathol Commun. 2014;2:137 pubmed 出版商
|
| Dwight T, Mann K, Benn D, Robinson B, McKelvie P, Gill A, et al. Familial SDHA mutation associated with pituitary adenoma and pheochromocytoma/paraganglioma. J Clin Endocrinol Metab. 2013;98:E1103-8 pubmed 出版商
|
| Jourdain A, Koppen M, Wydro M, Rodley C, Lightowlers R, Chrzanowska Lightowlers Z, et al. GRSF1 regulates RNA processing in mitochondrial RNA granules. Cell Metab. 2013;17:399-410 pubmed 出版商
|
| Dwight T, Benn D, Clarkson A, Vilain R, Lipton L, Robinson B, et al. Loss of SDHA expression identifies SDHA mutations in succinate dehydrogenase-deficient gastrointestinal stromal tumors. Am J Surg Pathol. 2013;37:226-33 pubmed 出版商
|
| Welander J, Larsson C, Bäckdahl M, Hareni N, Sivlér T, Brauckhoff M, et al. Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas. Hum Mol Genet. 2012;21:5406-16 pubmed 出版商
|
| Chou A, Chen J, Clarkson A, Samra J, Clifton Bligh R, Hugh T, et al. Succinate dehydrogenase-deficient GISTs are characterized by IGF1R overexpression. Mod Pathol. 2012;25:1307-13 pubmed 出版商
|
| He J, Cooper H, Reyes A, Di Re M, Sembongi H, Litwin T, et al. Mitochondrial nucleoid interacting proteins support mitochondrial protein synthesis. Nucleic Acids Res. 2012;40:6109-21 pubmed 出版商
|
| Shan Y, Cortopassi G. HSC20 interacts with frataxin and is involved in iron-sulfur cluster biogenesis and iron homeostasis. Hum Mol Genet. 2012;21:1457-69 pubmed 出版商
|
| Celestino R, Lima J, Faustino A, Máximo V, Gouveia A, Vinagre J, et al. A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney-Stratakis dyad. Fam Cancer. 2012;11:189-94 pubmed 出版商
|
| Miettinen M, Wang Z, Sarlomo Rikala M, Osuch C, Rutkowski P, Lasota J. Succinate dehydrogenase-deficient GISTs: a clinicopathologic, immunohistochemical, and molecular genetic study of 66 gastric GISTs with predilection to young age. Am J Surg Pathol. 2011;35:1712-21 pubmed 出版商
|
| Rossi S, Miceli R, Messerini L, Bearzi I, Mazzoleni G, Capella C, et al. Natural history of imatinib-naive GISTs: a retrospective analysis of 929 cases with long-term follow-up and development of a survival nomogram based on mitotic index and size as continuous variables. Am J Surg Pathol. 2011;35:1646-56 pubmed 出版商
|
| Gill A, Pachter N, Chou A, Young B, Clarkson A, Tucker K, et al. Renal tumors associated with germline SDHB mutation show distinctive morphology. Am J Surg Pathol. 2011;35:1578-85 pubmed 出版商
|
| Wang J, Lasota J, Miettinen M. Succinate Dehydrogenase Subunit B (SDHB) Is Expressed in Neurofibromatosis 1-Associated Gastrointestinal Stromal Tumors (Gists): Implications for the SDHB Expression Based Classification of Gists. J Cancer. 2011;2:90-3 pubmed
|
| Ferreira M, Torraco A, Rizza T, Fattori F, Meschini M, Castana C, et al. Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1. Neurogenetics. 2011;12:9-17 pubmed 出版商
|
| STRUB G, Paillard M, Liang J, Gomez L, Allegood J, Hait N, et al. Sphingosine-1-phosphate produced by sphingosine kinase 2 in mitochondria interacts with prohibitin 2 to regulate complex IV assembly and respiration. FASEB J. 2011;25:600-12 pubmed 出版商
|
| Gerards M, van den Bosch B, Danhauser K, Serre V, van Weeghel M, Wanders R, et al. Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene. Brain. 2011;134:210-9 pubmed 出版商
|
| Cameron J, Levandovskiy V, Mackay N, Ackerley C, Chitayat D, Raiman J, et al. Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization. Mitochondrion. 2011;11:191-9 pubmed 出版商
|
| Gegg M, Cooper J, Chau K, Rojo M, Schapira A, Taanman J. Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy. Hum Mol Genet. 2010;19:4861-70 pubmed 出版商
|
| Fassone E, Duncan A, Taanman J, Pagnamenta A, Sadowski M, Holand T, et al. FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy. Hum Mol Genet. 2010;19:4837-47 pubmed 出版商
|
| Tuppen H, Hogan V, He L, Blakely E, Worgan L, Al Dosary M, et al. The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families. Brain. 2010;133:2952-63 pubmed 出版商
|
| Mayr J, Havlíčková V, Zimmermann F, Magler I, Kaplanová V, Jesina P, et al. Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit. Hum Mol Genet. 2010;19:3430-9 pubmed 出版商
|
| Calore F, Genisset C, Casellato A, Rossato M, Codolo G, Esposti M, et al. Endosome-mitochondria juxtaposition during apoptosis induced by H. pylori VacA. Cell Death Differ. 2010;17:1707-16 pubmed 出版商
|
| Ylikallio E, Tyynismaa H, Tsutsui H, Ide T, Suomalainen A. High mitochondrial DNA copy number has detrimental effects in mice. Hum Mol Genet. 2010;19:2695-705 pubmed 出版商
|
| Feichtinger R, Zimmermann F, Mayr J, Neureiter D, Hauser Kronberger C, Schilling F, et al. Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma. BMC Cancer. 2010;10:149 pubmed 出版商
|
| Gill A, Chou A, Vilain R, Clarkson A, Lui M, JIN R, et al. Immunohistochemistry for SDHB divides gastrointestinal stromal tumors (GISTs) into 2 distinct types. Am J Surg Pathol. 2010;34:636-44 pubmed 出版商
|
| Gill A, Benn D, Chou A, Clarkson A, Muljono A, Meyer Rochow G, et al. Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC, and SDHD in paraganglioma-pheochromocytoma syndromes. Hum Pathol. 2010;41:805-14 pubmed 出版商
|
| Walmsley S, Broeckling C, Hess A, Prenni J, Curthoys N. Proteomic analysis of brush-border membrane vesicles isolated from purified proximal convoluted tubules. Am J Physiol Renal Physiol. 2010;298:F1323-31 pubmed 出版商
|
| Ahola Erkkilä S, Carroll C, Peltola Mjösund K, Tulkki V, Mattila I, Seppanen Laakso T, et al. Ketogenic diet slows down mitochondrial myopathy progression in mice. Hum Mol Genet. 2010;19:1974-84 pubmed 出版商
|
| Wydro M, Bobrowicz A, Temperley R, Lightowlers R, Chrzanowska Lightowlers Z. Targeting of the cytosolic poly(A) binding protein PABPC1 to mitochondria causes mitochondrial translation inhibition. Nucleic Acids Res. 2010;38:3732-42 pubmed 出版商
|
| Fogal V, Richardson A, Karmali P, Scheffler I, Smith J, Ruoslahti E. Mitochondrial p32 protein is a critical regulator of tumor metabolism via maintenance of oxidative phosphorylation. Mol Cell Biol. 2010;30:1303-18 pubmed 出版商
|
| Kachadourian R, Brechbuhl H, Ruiz Azuara L, Gracia Mora I, Day B. Casiopeína IIgly-induced oxidative stress and mitochondrial dysfunction in human lung cancer A549 and H157 cells. Toxicology. 2010;268:176-83 pubmed 出版商
|
| Cimen H, Han M, Yang Y, Tong Q, Koc H, Koc E. Regulation of succinate dehydrogenase activity by SIRT3 in mammalian mitochondria. Biochemistry. 2010;49:304-11 pubmed 出版商
|
| Mracek T, Gao D, Tzanavari T, Bao Y, Xiao X, Stocker C, et al. Downregulation of zinc-{alpha}2-glycoprotein in adipose tissue and liver of obese ob/ob mice and by tumour necrosis factor-alpha in adipocytes. J Endocrinol. 2010;204:165-72 pubmed 出版商
|
| Horvath R, Kemp J, Tuppen H, Hudson G, Oldfors A, Marie S, et al. Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy. Brain. 2009;132:3165-74 pubmed 出版商
|
| Gómez L, Monette J, Chavez J, Maier C, Hagen T. Supercomplexes of the mitochondrial electron transport chain decline in the aging rat heart. Arch Biochem Biophys. 2009;490:30-5 pubmed 出版商
|
| Gerards M, Sluiter W, van den Bosch B, de Wit L, Calis C, Frentzen M, et al. Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. J Med Genet. 2010;47:507-12 pubmed 出版商
|
| Brennan L, Lee W, Cowell T, Giblin F, Kantorow M. Deletion of mouse MsrA results in HBO-induced cataract: MsrA repairs mitochondrial cytochrome c. Mol Vis. 2009;15:985-99 pubmed
|
| Burnichon N, Rohmer V, Amar L, Herman P, Leboulleux S, Darrouzet V, et al. The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. J Clin Endocrinol Metab. 2009;94:2817-27 pubmed 出版商
|
| Yahata N, Yuasa S, Araki T. Nicotinamide mononucleotide adenylyltransferase expression in mitochondrial matrix delays Wallerian degeneration. J Neurosci. 2009;29:6276-84 pubmed 出版商
|
| Hanein S, Perrault I, Roche O, Gerber S, Khadom N, Rio M, et al. TMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive nonsyndromic optic atrophy. Am J Hum Genet. 2009;84:493-8 pubmed 出版商
|
| Son M, Fu Q, Puttaparthi K, Matthews C, Elliott J. Redox susceptibility of SOD1 mutants is associated with the differential response to CCS over-expression in vivo. Neurobiol Dis. 2009;34:155-62 pubmed
|
| Jeong K, Kwon H, Min C, Pak Y. Modulation of the caveolin-3 localization to caveolae and STAT3 to mitochondria by catecholamine-induced cardiac hypertrophy in H9c2 cardiomyoblasts. Exp Mol Med. 2009;41:226-35 pubmed 出版商
|
| De Maria A, Shi Y, Kumar N, Bassnett S. Calpain expression and activity during lens fiber cell differentiation. J Biol Chem. 2009;284:13542-50 pubmed 出版商
|
| Caro P, Gomez J, Sanchez I, Garcia R, Lopez Torres M, Naudi A, et al. Effect of 40% restriction of dietary amino acids (except methionine) on mitochondrial oxidative stress and biogenesis, AIF and SIRT1 in rat liver. Biogerontology. 2009;10:579-92 pubmed 出版商
|
| Calvaruso M, Smeitink J, Nijtmans L. Electrophoresis techniques to investigate defects in oxidative phosphorylation. Methods. 2008;46:281-7 pubmed 出版商
|
| Ahn B, Kim H, Song S, Lee I, Liu J, Vassilopoulos A, et al. A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis. Proc Natl Acad Sci U S A. 2008;105:14447-52 pubmed 出版商
|
| Rorbach J, Richter R, Wessels H, Wydro M, Pekalski M, Farhoud M, et al. The human mitochondrial ribosome recycling factor is essential for cell viability. Nucleic Acids Res. 2008;36:5787-99 pubmed 出版商
|
| Hakonen A, Goffart S, Marjavaara S, Paetau A, Cooper H, Mattila K, et al. Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion. Hum Mol Genet. 2008;17:3822-35 pubmed 出版商
|
| Murayama K, Nagasaka H, Tsuruoka T, Omata Y, Horie H, Tregoning S, et al. Intractable secretory diarrhea in a Japanese boy with mitochondrial respiratory chain complex I deficiency. Eur J Pediatr. 2009;168:297-302 pubmed 出版商
|
| Son M, Leary S, Romain N, Pierrel F, Winge D, Haller R, et al. Isolated cytochrome c oxidase deficiency in G93A SOD1 mice overexpressing CCS protein. J Biol Chem. 2008;283:12267-75 pubmed 出版商
|
| Fornuskova D, Brantova O, Tesarova M, Stiburek L, Honzik T, Wenchich L, 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. 2008;1782:317-25 pubmed 出版商
|
| Lyly A, Marjavaara S, Kyttälä A, Uusi Rauva K, Luiro K, Kopra O, et al. Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism. Hum Mol Genet. 2008;17:1406-17 pubmed 出版商
|
| Lebon S, Minai L, Chretien D, Corcos J, Serre V, Kadhom N, 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. 2007;92:104-8 pubmed
|
| Canal F, Fosset C, Chauveau M, Drapier J, Bouton C. Regulation of the cysteine desulfurase Nfs1 and the scaffold protein IscU in macrophages stimulated with interferon-gamma and lipopolysaccharide. Arch Biochem Biophys. 2007;465:282-92 pubmed
|
| Li Y, D Aurelio M, Deng J, Park J, Manfredi G, Hu P, et al. An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria. J Biol Chem. 2007;282:17557-62 pubmed
|
| Ramanujan V, Herman B. Aging process modulates nonlinear dynamics in liver cell metabolism. J Biol Chem. 2007;282:19217-26 pubmed
|
| Park J, Li Y, Bai Y. 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. 2007;1772:533-42 pubmed
|
| Carrozzo R, Dionisi Vici C, Steuerwald U, Lucioli S, Deodato F, Di Giandomenico S, et al. SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. Brain. 2007;130:862-74 pubmed
|
| Folbergrová J, Jesina P, Drahota Z, Lisy V, Haugvicova R, Vojtiskova A, et al. Mitochondrial complex I inhibition in cerebral cortex of immature rats following homocysteic acid-induced seizures. Exp Neurol. 2007;204:597-609 pubmed
|
| Lelliott C, Medina Gomez G, Petrovic N, Kis A, Feldmann H, Bjursell M, et al. Ablation of PGC-1beta results in defective mitochondrial activity, thermogenesis, hepatic function, and cardiac performance. PLoS Biol. 2006;4:e369 pubmed
|
| Yoon Y, Yoon D, Lim I, Yoon S, Chung H, Rojo M, et al. Formation of elongated giant mitochondria in DFO-induced cellular senescence: involvement of enhanced fusion process through modulation of Fis1. J Cell Physiol. 2006;209:468-80 pubmed
|
| Powelka A, Seth A, Virbasius J, Kiskinis E, Nicoloro S, Guilherme A, et al. Suppression of oxidative metabolism and mitochondrial biogenesis by the transcriptional corepressor RIP140 in mouse adipocytes. J Clin Invest. 2006;116:125-36 pubmed
|