UCP2 overexpression worsens mitochondrial dysfunction and accelerates disease progression in a mouse model of amyotrophic lateral sclerosis.
about
Role of mitochondria in mutant SOD1 linked amyotrophic lateral sclerosisElevated mRNA-levels of distinct mitochondrial and plasma membrane Ca(2+) transporters in individual hypoglossal motor neurons of endstage SOD1 transgenic mice.Seeking homeostasis: temporal trends in respiration, oxidation, and calcium in SOD1 G93A Amyotrophic Lateral Sclerosis mice.Rosmarinic Acid Alleviates Neurological Symptoms in the G93A-SOD1 Transgenic Mouse Model of Amyotrophic Lateral Sclerosis.Uncoupling Protein 2 Increases Susceptibility to Lipopolysaccharide-Induced Acute Lung Injury in MicePerspectives on mitochondrial uncoupling proteins-mediated neuroprotection.AMPK Signalling and Defective Energy Metabolism in Amyotrophic Lateral Sclerosis.Therapeutic Potential of Genipin in Central Neurodegenerative Diseases.Uncoupling protein 2 and metabolic diseases.Metabolic Vulnerability in the Neurodegenerative Disease Glaucoma.Brain and Peripheral Atypical Inflammatory Mediators Potentiate Neuroinflammation and Neurodegeneration.Effects of Mitochondrial Uncoupling Protein 2 Inhibition by Genipin in Human Cumulus Cells.The emerging role of immune dysfunction in mitochondrial diseases as a paradigm for understanding immunometabolism.Metabolic Reprogramming in Amyotrophic Lateral Sclerosis.Uncoupling Protein 2 in Cardiovascular Health and DiseaseDysregulation of MicroRNAs and Target Genes Networks in Peripheral Blood of Patients With Sporadic Amyotrophic Lateral Sclerosis
P2860
Q33819255-02267C97-9CA9-4F3B-9C03-1EC10EDC82D1Q35469175-B4026E94-C7D5-448A-ACF6-A61D2B5BC8D1Q35802837-1FE9F85E-9E06-4A35-96DA-1EB4412D6407Q36396423-904D331C-72FD-4308-B543-10C617D86AE3Q36600608-27603E0F-5876-47FE-808E-9A81B8AC0138Q38248841-44507249-F76C-4463-8BE4-2107E1DAD945Q38552413-05D171DC-47BA-4F6A-8D69-5081EA0E0114Q38891142-7C669985-8D44-4212-9465-EE2650FB97C2Q39205505-88B5B4DD-5AE9-4A5D-8361-EF762F2E9876Q39251141-DAAD4458-A448-46C0-97D5-F24305A0D7E4Q41097407-4B257EEE-8CCF-4E04-A738-FFA099049227Q43034930-03AA8401-811F-4709-BAC5-C3F51614B7BAQ49835166-C4AF6BBD-EAE0-45C4-B600-3945DDEB0781Q51736520-D458A1CB-702A-44D4-ADBF-AA60DE458AF4Q58335880-BB64C5FB-C85C-45E8-952A-278987CDC872Q58698224-AD54985F-F605-488D-B0CA-1AE6C7DE0511
P2860
UCP2 overexpression worsens mitochondrial dysfunction and accelerates disease progression in a mouse model of amyotrophic lateral sclerosis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 17 October 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
UCP2 overexpression worsens mi ...... amyotrophic lateral sclerosis.
@en
UCP2 overexpression worsens mi ...... amyotrophic lateral sclerosis.
@nl
type
label
UCP2 overexpression worsens mi ...... amyotrophic lateral sclerosis.
@en
UCP2 overexpression worsens mi ...... amyotrophic lateral sclerosis.
@nl
prefLabel
UCP2 overexpression worsens mi ...... amyotrophic lateral sclerosis.
@en
UCP2 overexpression worsens mi ...... amyotrophic lateral sclerosis.
@nl
P2093
P2860
P921
P1476
UCP2 overexpression worsens mi ...... amyotrophic lateral sclerosis.
@en
P2093
Brittany Sider
Giovanni Manfredi
Hyun-Jeong Kim
Tamas L Horvath
P2860
P304
P356
10.1016/J.MCN.2013.10.002
P577
2013-10-17T00:00:00Z