Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases. - Wikidata - awgldk - TriplyDB

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

http://www.wikidata.org/entity/Q37775036

about

Cell signaling and mitochondrial dynamics: Implications for neuronal function and neurodegenerative disease Proteomics of protein post-translational modifications implicated in neurodegeneration Accumulation of Basic Amino Acids at Mitochondria Dictates the Cytotoxicity of Aberrant Ubiquitin Quality control of mitochondrial proteostasis.New insight into neurodegeneration: the role of proteomics.Drosophila as a potential model to ameliorate mutant Huntington-mediated cardiac amyloidosis Phenotyping of tianma-stimulated differentiated rat neuronal b104 cells by quantitative proteomics.Ginkgo extract EGb 761(®) shields from slowly accumulating neurodegenerative-like changes in a newly developed cell culture model induced by the combined action of low doses of antimycin A1 and 2-deoxy-D-glucose.In-depth phenotyping of lymphoblastoid cells suggests selective cellular vulnerability in Marinesco-Sjögren syndrome.

P2860

Q26853356-4D522B49-D768-4683-AC12-CC3728BBC6B7 Q28088631-2481D2AA-C033-4CD0-AD66-78819589893C Q35529325-D7D1AD66-7B10-499E-AF67-0F75DF735053 Q37882863-01876084-89B7-4211-A9FE-42878C41A32B Q38170010-2E23AA22-3D1A-4E10-89D7-D70926E2E6C0 Q38498245-7A75A90D-2007-47A9-97F3-423CD40432F9 Q39441306-37F8AEE2-0BAE-4ACF-9FB3-C1968000CEE6 Q39561320-4A2CDF15-3FC5-4DDC-AFA8-1A54F59ED027 Q42366628-ADA874E8-7C66-419C-A206-A9099E701622

P2860

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

http://www.wikidata.org/entity/Q37775036

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on August 2010

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

@en

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

@nl

type

label

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

@en

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

@nl

prefLabel

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

@en

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

@nl

P1433

Q37775036-13D764E2-E04E-44A4-A2CD-701B0454A648

P1476

Q37775036-B2B6054C-1F5F-482F-A33E-052161BBC8F4

P2093

Q37775036-85CE070D-6834-4480-8778-E9CC94862AF0

Q37775036-97D1F95D-ED85-42B8-95B8-7651DA37A161

Q37775036-991E8F70-BC6D-443F-BF79-712CBE3A906D

Q37775036-A1491358-B1E1-4E08-B24E-944B40714A5C

Q37775036-C9FBBD33-F9B4-40AC-A5AD-3D24F39E019D

P2860

Q37775036-019610C8-8AD2-4B30-A71C-2570F8629B37

Q37775036-03822F90-28CF-4BED-8C33-F316D1A6BA20

Q37775036-03A1900F-47FD-4FFA-B77F-42FD5ADEB923

Q37775036-03FB60C7-A950-4D51-9F19-3320159DD6AE

Q37775036-05CBEBC8-0917-4ADE-906E-5ED0FC378EC5

Q37775036-06B270CA-1812-43B6-8AF0-89A0EC2F1FC2

Q37775036-0AB760D7-547A-4E51-8C1D-FEEFC4D8466B

Q37775036-0B6228BE-1BD9-4BDD-85C6-729B64A3B950

Q37775036-0B9CA786-1A8A-4834-AC77-10F778FDD04B

Q37775036-0BD093E1-EEC8-4E05-8201-D3D01FC913A3

P304

Q37775036-4E041140-3ED2-4B1D-9BA5-BB3696DFF9B4

P31

Q37775036-561EF23D-8766-4FD9-BE47-BB274005F1BC

P356

Q37775036-5E35850F-14CA-4973-A5E2-53195171DDE4

P433

Q37775036-65303ADE-E8CA-4F3B-8BB3-6B2E71FA5CA7

P478

Q37775036-50350915-C4C1-4617-91E6-028191C75640

P577

Q37775036-2212C88C-DB7F-4BC5-AFCA-795CD8CCE637

P5875

Q37775036-A22FA272-7CCD-4120-9EC9-8F4B17D3C34A

P698

Q37775036-290EA34E-617A-4A6D-A2CD-F7D6A5EE2790

P921

Q37775036-266EAE2C-001C-4B34-8C13-D4284CAABBB4

Q37775036-D67C972A-57C5-426B-9088-7C3CAF5F89C5

P356

P1433

Expert Review of Proteomics

P1476

Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.

@en

P2093

Carlo Rodolfo

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

Fabiola Ciccosanti

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

Gian Maria Fimia

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

Giuseppina Di Giacomo

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

Mauro Piacentini

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

P2860

Synapse Formation and Function Is Modulated by the Amyloid Precursor Protein

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

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

Huntington's disease genetics

PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1

Familial Alzheimer disease-linked mutations specifically disrupt Ca2+ leak function of presenilin 1

Mitochondrial localization of the Parkinson's disease related protein DJ-1: implications for pathogenesis

Proteomic analysis of increased Parkin expression and its interactants provides evidence for a role in modulation of mitochondrial function

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease

P304

519-542

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

P31

scholarly article

P356

10.1586/EPR.10.43

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

P433

4

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

P478

7

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

P577

2010-08-01T00:00:00Z

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

P5875

45284462

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

P698

20653508

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

P921

neurodegeneration