These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 12512346)

  • 21. Impairment in mitochondrial cytochrome oxidase gene expression in Alzheimer disease.
    Chandrasekaran K; Giordano T; Brady DR; Stoll J; Martin LJ; Rapoport SI
    Brain Res Mol Brain Res; 1994 Jul; 24(1-4):336-40. PubMed ID: 7968373
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cytochrome oxidase deficiency: clinical and biochemical heterogeneity.
    DiMauro S; Zeviani M; Servidei S; Bonilla E; Miranda AF; Prelle A; Schon EA
    Ann N Y Acad Sci; 1986; 488():19-32. PubMed ID: 3034115
    [No Abstract]   [Full Text] [Related]  

  • 23. Reduced mitochondria cytochrome oxidase activity in adult children of mothers with Alzheimer's disease.
    Mosconi L; de Leon M; Murray J; E L; Lu J; Javier E; McHugh P; Swerdlow RH
    J Alzheimers Dis; 2011; 27(3):483-90. PubMed ID: 21841246
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Dystrophic neurites of senile plaques in Alzheimer's disease are deficient in cytochrome c oxidase.
    Pérez-Gracia E; Torrejón-Escribano B; Ferrer I
    Acta Neuropathol; 2008 Sep; 116(3):261-8. PubMed ID: 18629521
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Decreased cytochrome-c oxidase activity and lack of age-related accumulation of mitochondrial DNA deletions in the brains of schizophrenics.
    Cavelier L; Jazin EE; Eriksson I; Prince J; Båve U; Oreland L; Gyllensten U
    Genomics; 1995 Sep; 29(1):217-24. PubMed ID: 8530074
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The T9861C Mutation in the mtDNA-Encoded Cytochrome C Oxidase Subunit III Gene Occurs in High Frequency but with Unequal Distribution in the Alzheimer's Disease Brain.
    Castora FJ; Conyers BL; Gershon BS; Kerns KA; Campbell R; Simsek-Duran F
    J Alzheimers Dis; 2019; 72(1):257-269. PubMed ID: 31561357
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency.
    Komaki H; Nishigaki Y; Fuku N; Hosoya H; Murayama K; Ohtake A; Goto Y; Wakamoto H; Koga Y; Tanaka M
    Biochim Biophys Acta; 2010 Mar; 1800(3):313-5. PubMed ID: 19616603
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Two point mutations in mitochondrial DNA of cytochrome c oxidase coexist with normal mtDNA in a patient with Alzheimer's disease.
    Qiu X; Chen Y; Zhou M
    Brain Res; 2001 Mar; 893(1-2):261-3. PubMed ID: 11223014
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Abnormality of the alpha-ketoglutarate dehydrogenase complex in fibroblasts from familial Alzheimer's disease.
    Sheu KF; Cooper AJ; Koike K; Koike M; Lindsay JG; Blass JP
    Ann Neurol; 1994 Mar; 35(3):312-8. PubMed ID: 8122883
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mild mitochondrial metabolic deficits by α-ketoglutarate dehydrogenase inhibition cause prominent changes in intracellular autophagic signaling: Potential role in the pathobiology of Alzheimer's disease.
    Banerjee K; Munshi S; Xu H; Frank DE; Chen HL; Chu CT; Yang J; Cho S; Kagan VE; Denton TT; Tyurina YY; Jiang JF; Gibson GE
    Neurochem Int; 2016 Jun; 96():32-45. PubMed ID: 26923918
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mitochondria and ageing.
    Müller-Höcker J
    Brain Pathol; 1992 Apr; 2(2):149-58. PubMed ID: 1341956
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Beta-amyloid inhibits integrated mitochondrial respiration and key enzyme activities.
    Casley CS; Canevari L; Land JM; Clark JB; Sharpe MA
    J Neurochem; 2002 Jan; 80(1):91-100. PubMed ID: 11796747
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inventory control: cytochrome c oxidase assembly regulates mitochondrial translation.
    Mick DU; Fox TD; Rehling P
    Nat Rev Mol Cell Biol; 2011 Jan; 12(1):14-20. PubMed ID: 21179059
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mitochondrial encephalomyopathies.
    DiMauro S
    Brain Pathol; 1992 Apr; 2(2):111-2. PubMed ID: 1341951
    [No Abstract]   [Full Text] [Related]  

  • 35. Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function.
    Fayet G; Jansson M; Sternberg D; Moslemi AR; Blondy P; Lombès A; Fardeau M; Oldfors A
    Neuromuscul Disord; 2002 Jun; 12(5):484-93. PubMed ID: 12031622
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer's disease.
    Bosetti F; Brizzi F; Barogi S; Mancuso M; Siciliano G; Tendi EA; Murri L; Rapoport SI; Solaini G
    Neurobiol Aging; 2002; 23(3):371-6. PubMed ID: 11959398
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A selective defect of cytochrome c oxidase is present in brain of Alzheimer disease patients.
    Maurer I; Zierz S; Möller HJ
    Neurobiol Aging; 2000; 21(3):455-62. PubMed ID: 10858595
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.
    Pancrudo J; Shanske S; Bonilla E; Daras M; Akman HO; Krishna S; Malkin E; DiMauro S
    J Child Neurol; 2007 Jul; 22(7):858-62. PubMed ID: 17715279
    [TBL] [Abstract][Full Text] [Related]  

  • 39. No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency.
    Parfait B; Percheron A; Chretien D; Rustin P; Munnich A; Rötig A
    Hum Genet; 1997 Dec; 101(2):247-50. PubMed ID: 9402980
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Isolated cytochrome c oxidase deficiency as a cause of MELAS.
    Rossmanith W; Freilinger M; Roka J; Raffelsberger T; Moser-Thier K; Prayer D; Bernert G; Bittner RE
    J Med Genet; 2008 Feb; 45(2):117-21. PubMed ID: 18245391
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.