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Mitochondrial haplogroups H and J: risk and protective factors for ischemic cardiomyopathyEvidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's diseaseMitochondrial DNA polymorphism A4917G is independently associated with age-related macular degenerationIterative orthology prediction uncovers new mitochondrial proteins and identifies C12orf62 as the human ortholog of COX14, a protein involved in the assembly of cytochrome c oxidaseThe mitochondrial DNA control region shows genetically correlated levels of heteroplasmy in leukocytes of centenarians and their offspringTreatment for mitochondrial disordersPentatricopeptide repeat domain protein 1 lowers the levels of mitochondrial leucine tRNAs in cellsRespiratory complex III is required to maintain complex I in mammalian mitochondriaMutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndromeCopper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiencyA mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiencyMutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegiaMay "mitochondrial eve" and mitochondrial haplogroups play a role in neurodegeneration and Alzheimer's disease?Multi-system neurological disease is common in patients with OPA1 mutationsMitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysisMolecular mechanisms of insulin resistance in humans and their potential links with mitochondrial dysfunctionDirect assignment of EPR spectra to structurally defined iron-sulfur clusters in complex I by double electron-electron resonanceMitochondrial defects in acute multiple sclerosis lesionsA mitochondrial protein compendium elucidates complex I disease biologyDistinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTsMitochondrial DNA mutations in human diseaseMitochondrial DNA mutations in cancer.Emerging therapeutic roles for NAD(+) metabolism in mitochondrial and age-related disordersThe Role of Organelle Stresses in Diabetes Mellitus and Obesity: Implication for TreatmentMitochondrial disease in childhood: nuclear encodedMitochondrial biology and Parkinson's diseaseLeber hereditary optic neuropathy: current perspectivesAlzheimer's pathogenesis and its link to the mitochondrionMitochondrial oxidative stress in aging and healthspanNear-infrared 808 nm light boosts complex IV-dependent respiration and rescues a Parkinson-related pink1 modelDetection of heteroplasmic mitochondrial DNA in single mitochondriaModes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunctionInhibitor-complexed structures of the cytochrome bc1 from the photosynthetic bacterium Rhodobacter sphaeroidesMdm38 interacts with ribosomes and is a component of the mitochondrial protein export machinery.Shy1 couples Cox1 translational regulation to cytochrome c oxidase assembly.Coa3 and Cox14 are essential for negative feedback regulation of COX1 translation in mitochondria.Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth SyndromeSending Out an SOS: Mitochondria as a Signaling HubOvercoming Challenges With Statin TherapyReactive Oxygen Species: A Key Hallmark of Cardiovascular Disease
P2860
Q21134066-3446749E-80A7-43D4-A6B5-1D6139657311Q21136190-A782784E-0D1F-4396-B38B-A993E3B5F339Q21144317-5548E778-44FF-4AF3-A066-49A6BFF71DF9Q21184006-D16B7D81-D8FD-42F4-A1C5-34290FD986C2Q21266560-46F469A1-0852-464D-B425-FDD018D638B0Q24200432-B550F765-B9B2-4139-AD69-5D043934AFF3Q24320144-2643F80C-5D27-48B0-B0CE-EA07257E00FAQ24322645-3061F884-3C1E-4CCA-9F29-17DFCA288240Q24337244-AFBE6733-A5C9-47CE-8392-27E297BE87A8Q24337613-22E8BAB7-822E-4590-B203-9AA054E6ED2FQ24540570-3D16DD99-C916-4499-A2C9-761F4BED7283Q24546476-49B6FBF0-F910-466F-ADC5-2686324C7513Q24600533-77142185-614C-4EEC-8963-D771922BAD54Q24619312-A30396A5-BC54-47FC-847A-3E4B221D664BQ24630557-C02DE5F1-9523-4880-88D0-0E6FB5F73581Q24632414-C5A6620B-9662-4E80-B3A5-B64E78C1C1F8Q24645274-5ABF921D-C473-4D4C-BC05-4039AB04C2D0Q24648580-74DFE6C6-9B91-4D39-9361-FC807EA96210Q24655079-CE8B9A1E-0673-44F4-91E2-9B3FFD454E64Q24672004-A89B09FD-6FE2-45D6-9D6F-BB4CD2FCCF37Q24676881-3106A8A5-7D09-4EA9-B9C3-7C8AC8010150Q24812627-EE886C47-2D54-401A-BAF6-A0FB53874D9EQ26741300-A9DB371C-932C-47C2-8783-4CF6C0B26406Q26776377-0727E3FD-54E1-4382-A637-44660955AA6DQ26820866-43F1D227-6068-49A2-8489-BA1545DF297DQ26824090-28572EF0-AA36-4DA4-97FF-4703B753A558Q26863599-3AC628D8-0F45-410E-AB25-083181EDEEFFQ27000255-AEBEA935-12FB-4C7C-B386-C12AE8B4F3D1Q27025099-50118390-11D5-45B6-9F56-EB1AC9DE0C08Q27303071-0D14F690-3D70-44EF-9340-FC7CC956A10AQ27315184-34EF4B24-DF9A-4ADD-A3C7-A481BE5DB508Q27317174-BD38FB5C-DF6E-4E39-B5B7-C420C2BCF79AQ27649140-53B500DE-2F99-4494-BF59-7901F1ED39F3Q27930074-CED1B68E-0F09-444F-A9EE-ED79C6A77E70Q27933832-93010AAC-4BA0-4D5E-AB20-8765096DFB87Q27936564-5605A696-F020-4F3E-8028-F1BD470B3B73Q27936928-B144EE68-EF68-4C3A-BDCC-127B2F66C828Q28073077-7E0067ED-3EB2-4DDD-8182-7EC7C6A5D241Q28073319-5EE45933-CA2C-47CC-995B-C3F712ADB8FFQ28076240-C128BA10-4C25-4C4F-8549-FEEF21B6EB21
P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Mitochondrial respiratory-chain diseases
@ast
Mitochondrial respiratory-chain diseases
@en
type
label
Mitochondrial respiratory-chain diseases
@ast
Mitochondrial respiratory-chain diseases
@en
prefLabel
Mitochondrial respiratory-chain diseases
@ast
Mitochondrial respiratory-chain diseases
@en
P3181
P356
P1476
Mitochondrial respiratory-chain diseases
@en
P2093
P304
P3181
P356
10.1056/NEJMRA022567
P407
P577
2003-06-26T00:00:00Z