Complex I deficiency in Parkinson's disease frontal cortex. - Wikidata - awgldk - TriplyDB

Complex I deficiency in Parkinson's disease frontal cortex.

Complex I deficiency in Parkinson's disease frontal cortex.

http://www.wikidata.org/entity/Q30440448

about

The role of oxidative stress in Parkinson's disease Parkin-dependent degradation of the F-box protein Fbw7β promotes neuronal survival in response to oxidative stress by stabilizing Mcl-1 PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling microRNAs: Emerging Targets Regulating Oxidative Stress in the Models of Parkinson's Disease Parkinson's Disease: The Mitochondria-Iron Link The Role of Autophagy, Mitophagy and Lysosomal Functions in Modulating Bioenergetics and Survival in the Context of Redox and Proteotoxic Damage: Implications for Neurodegenerative Diseases Oncostatic-Cytoprotective Effect of Melatonin and Other Bioactive Molecules: A Common Target in Mitochondrial Respiration Electron Transport Disturbances and Neurodegeneration: From Albert Szent-Györgyi's Concept (Szeged) till Novel Approaches to Boost Mitochondrial Bioenergetics Oxidative stress and Parkinson's disease Cerebral energy metabolism and the brain's functional network architecture: an integrative review Oxidative stress and cerebral endothelial cells: regulation of the blood-brain-barrier and antioxidant based interventions Genetically engineered mouse models of Parkinson's disease Metabolic disturbances in diseases with neurological involvement Mitochondrial dysfunction and oxidative stress in Parkinson's disease Bioenergetic adaptation in response to autophagy regulators during rotenone exposure Identification of licopyranocoumarin and glycyrurol from herbal medicines as neuroprotective compounds for Parkinson's disease Stem cell-based models and therapies for neurodegenerative diseases DJ-1 knock-down impairs astrocyte mitochondrial function.Oxidative stress in skin fibroblasts cultures from patients with Parkinson's disease Decylubiquinone increases mitochondrial function in synaptosomes Brain mitochondria from DJ-1 knockout mice show increased respiration-dependent hydrogen peroxide consumption.Neuroproteomics as a promising tool in Parkinson's disease research.Mitochondrial dysfunction in the limelight of Parkinson's disease pathogenesis.Lysosomal function in macromolecular homeostasis and bioenergetics in Parkinson's disease.The neurodegenerative mitochondriopathies.Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model.Distinct effects of rotenone, 1-methyl-4-phenylpyridinium and 6-hydroxydopamine on cellular bioenergetics and cell death.PINK1 and Parkin to control mitochondria remodeling.Enhanced glutamate, IP3 and cAMP activity in the cerebral cortex of unilateral 6-hydroxydopamine induced Parkinson's rats: effect of 5-HT, GABA and bone marrow cell supplementation.Decreased glutamic acid decarboxylase mRNA expression in prefrontal cortex in Parkinson's disease.Central pathways causing fatigue in neuro-inflammatory and autoimmune illnesses.Mice lacking TR4 nuclear receptor develop mitochondrial myopathy with deficiency in complex I.N-terminal truncated UCH-L1 prevents Parkinson's disease associated damage.High-level inhibition of mitochondrial complexes III and IV is required to increase glutamate release from the nerve terminal.The many roads to mitochondrial dysfunction in neuroimmune and neuropsychiatric disorders Mitochondrial Dysfunction and α-Synuclein Synaptic Pathology in Parkinson's Disease: Who's on First?Mask loss-of-function rescues mitochondrial impairment and muscle degeneration of Drosophila pink1 and parkin mutants Early Expression of Parkinson's Disease-Related Mitochondrial Abnormalities in PINK1 Knockout Rats.Mitochondrial dysfunction in genetic animal models of Parkinson's disease

P2860

Q24307946-91E5947D-DB9A-4C48-8F71-CB95D878CC7E Q24308897-DD5C5753-365F-4641-9747-800365CB06AB Q24597726-8E78D704-3B2E-4502-A784-32C3CD1A4507 Q24608960-33A284CF-7ED9-4736-96CC-17B6512B497A Q26738440-B5BC7586-A958-49E4-B2A8-F03D0AB26587 Q26746899-9E650F5F-2A43-41FD-8D75-DEA0579212FF Q26750137-B9C587C2-9365-4635-920A-139662E84A1B Q26766876-60FE9852-5E96-433E-8547-6F5D71F275BE Q26795417-50E62F6D-1BB8-43F6-BCEE-BAA386BB8667 Q26798897-DBFFBD75-5268-4C58-BEC4-D6DB7B63C3BA Q26830365-27FA04DB-34F2-45FF-A2BA-59300F0A591B Q26851676-42461369-82F0-453F-AC20-5DEB4EA8D0F3 Q26852964-26CE50B5-D575-4C63-B084-4FB8B660E336 Q26999015-763ACEB1-D521-484D-9C12-695ACF52AC9F Q27014051-15AAFEA4-58DA-405D-8F5E-69A74B0A9B31 Q28395471-BE31EC38-B173-4216-BF2D-7ED787C3CFCB Q28539943-ED65A35E-944F-4144-8331-C2CE8B70B694 Q30451005-69917B61-0334-4443-BCCE-C9736526D45E Q30527966-6AA396B6-F7BC-41D3-9373-2025E2335B87 Q33722784-FEF3B8FD-2975-495F-B88C-C97D93CBEF1F Q33726402-E6139D44-A7D6-47D7-827B-E657585EAD2F Q33737338-2FAC02CA-B01D-4356-AFF1-FCC87ECD6B94 Q33821316-49A99B65-EA37-4D4A-BAAA-BA3CB918F95A Q33840243-E6525B12-8D38-47A3-B74C-62C7004DFBBB Q33843073-90F2AAD7-9C92-4B43-9684-A213A361889A Q33957065-4D6E7BF6-505A-4B80-AABC-51B511DBE58D Q34368460-73CCBF51-B967-49B1-B007-64BC9FA95A48 Q34412601-3DCA032B-7D2B-4007-BD32-20F6ACB47CAF Q34462283-9B58B49A-C6D9-405E-A393-9E465DE9F47A Q34521827-A1F2286D-901A-40F2-A0A4-65F881E3E3F0 Q35024422-3CB115BE-CCF2-4E3C-A19F-C6F62DD118BB Q35059951-8B48AF13-9339-449B-81A8-0C0126642F66 Q35135711-BF96C9B0-E1FC-41FE-9AED-F7D8A039F65B Q35193829-2701CC6E-1224-4534-83B5-80A9C868B351 Q35203821-E1E99B07-3B24-4893-BE21-082480690DA4 Q35246024-DE782C15-4657-441F-B380-E77728E6D3E9 Q35412397-9DAC7053-54F4-4AD4-8ADA-9CABDEA36033 Q35585304-20ABCB71-2940-43A2-BAF3-38423A028EE9 Q35642539-B03140A1-F0BF-4FDB-8166-C4EA406DB046 Q35799109-704D18B6-19B9-4791-96E3-7EA1FBF7257C

P2860

Complex I deficiency in Parkinson's disease frontal cortex.

http://www.wikidata.org/entity/Q30440448

description

2007 nî lūn-bûn

@nan

2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Complex I deficiency in Parkinson's disease frontal cortex.

@ast

Complex I deficiency in Parkinson's disease frontal cortex.

@en

type

label

Complex I deficiency in Parkinson's disease frontal cortex.

@ast

Complex I deficiency in Parkinson's disease frontal cortex.

@en

prefLabel

Complex I deficiency in Parkinson's disease frontal cortex.

@ast

Complex I deficiency in Parkinson's disease frontal cortex.

@en

P1433

Q30440448-48C4FD8A-1CA7-4809-8A6F-67E02EDE9A3E

P1476

Q30440448-0EFA04EC-785F-4960-A807-A078BF6205D4

P2093

Q30440448-33EA0E3B-DB00-4DEF-8729-5DA4C6D48A8B

Q30440448-4AD1D8D9-E199-44A2-9EC4-7F61D5B29022

Q30440448-88368476-9F0F-41A0-B804-622DECC9A50B

P2860

Q30440448-00C05C9B-84CC-4B34-8104-14455D99F6AE

Q30440448-0E5D3129-876D-444C-BA78-1A8804F5C764

Q30440448-224FAC99-B28E-4A39-92D0-C8B6317B8F48

Q30440448-39601911-BFA8-4978-A079-73F6E31130C1

Q30440448-3A9EA2FB-C5D3-488F-A993-B3DDDA296418

Q30440448-3FAC1B59-5B42-46E0-9A04-C6D461ABA734

Q30440448-5640C9C5-6425-4451-B0C9-CBB5F42B1AB2

Q30440448-5DA910C8-C924-4496-8E68-C5E28A35B008

Q30440448-6E002E55-4F1D-470C-9936-D129E64B38EA

Q30440448-94AD9E59-9850-4E1B-9099-62D4FE4F43A7

P304

Q30440448-432C9FDE-FA93-4DAF-922E-B4878170B33F

P31

Q30440448-AAFF1D2B-E08A-45EB-880B-E5FC8C598285

P356

Q30440448-0D4789B4-8DF3-4D8D-8FC6-9E1F20F74181

P407

Q30440448-154F47F3-2B7B-4FC7-837F-2E6E89D4CD81

P478

Q30440448-70CB7869-D8BB-49BF-8A83-FF2800E9B9D4

P577

Q30440448-DDF4E9E1-0ECE-4905-AB38-0130C96DA82C

P5875

Q30440448-345B796B-8AFE-4737-9EF2-EFC655FEBF7D

P698

Q30440448-F629A15B-614A-48ED-835E-FC62AF60148B

P921

Q30440448-C2FEE830-A7A0-4DDE-AA7F-9637D34F98CA

P932

Q30440448-E041083F-0F8A-4041-A3B8-2C30E1153F1A

P356

J.BRAINRES.2007.10.061

P1433

P1476

Complex I deficiency in Parkinson's disease frontal cortex.

@en

P2093

Janice K Parks

http://www.w3.org/2001/XMLSchema#string

Russell H Swerdlow

http://www.w3.org/2001/XMLSchema#string

W Davis Parker

http://www.w3.org/2001/XMLSchema#string

P2860

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

Mitochondria in Alzheimer's disease.

High frequency of mitochondrial complex I mutations in Parkinson's disease and aging.

Mitochondrial ND5 mutations in idiopathic Parkinson's disease.

Genetic algorithm for analysis of mutations in Parkinson's disease.

Origin and functional consequences of the complex I defect in Parkinson's disease.

Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease.

Mitochondria - the Kraken wakes!

An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.

P304

215-218

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.BRAINRES.2007.10.061

http://www.w3.org/2001/XMLSchema#string

P407

P478

1189

http://www.w3.org/2001/XMLSchema#string

P577

2007-11-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5787347

http://www.w3.org/2001/XMLSchema#string

P698

18061150

http://www.w3.org/2001/XMLSchema#string

P921

Parkinson's disease

P932

2295283

http://www.w3.org/2001/XMLSchema#string