Suppression of the JNK pathway by induction of a metabolic stress response prevents vascular injury and dysfunction. - Wikidata - awgldk - TriplyDB

Suppression of the JNK pathway by induction of a metabolic stress response prevents vascular injury and dysfunction.

Suppression of the JNK pathway by induction of a metabolic stress response prevents vascular injury and dysfunction.

http://www.wikidata.org/entity/Q37372989

about

Pathogenesis of endothelial cell dysfunction in chronic kidney disease: a retrospective and what the future may hold AMPK: a cellular metabolic and redox sensor. A minireview After the banquet: mitochondrial biogenesis, mitophagy, and cell survival Methotrexate-mediated activation of an AMPK-CREB-dependent pathway: a novel mechanism for vascular protection in chronic systemic inflammation Noise-Induced Loss of Hair Cells and Cochlear Synaptopathy Are Mediated by the Activation of AMPK.Mitochondria, endothelial cell function, and vascular diseases.Concerted regulation of cGMP and cAMP phosphodiesterases in early cardiac hypertrophy induced by angiotensin II Shear stress, SIRT1, and vascular homeostasis.Molecular insights and therapeutic targets for diabetic endothelial dysfunction.Mechanisms of vascular aging: new perspectives.Exposure to hydrogen peroxide induces oxidation and activation of AMP-activated protein kinase.Adenosine monophosphate-activated protein kinase induces cholesterol efflux from macrophage-derived foam cells and alleviates atherosclerosis in apolipoprotein E-deficient mice.Activation of AMPK stimulates heme oxygenase-1 gene expression and human endothelial cell survival.Endothelial AMPK activation induces mitochondrial biogenesis and stress adaptation via eNOS-dependent mTORC1 signaling.Adipocyte heme oxygenase-1 induction attenuates metabolic syndrome in both male and female obese mice.Novel ferrocenyl derivatives exert anti-cancer effect in human lung cancer cells in vitro via inducing G1-phase arrest and senescence.AMPK in cardiovascular health and disease.Compound C stimulates heme oxygenase-1 gene expression via the Nrf2-ARE pathway to preserve human endothelial cell survival.Pre-B-cell colony-enhancing factor exerts a neuronal protection through its enzymatic activity and the reduction of mitochondrial dysfunction in in vitro ischemic models.High fat diet enhances cardiac abnormalities in SHR rats: Protective role of heme oxygenase-adiponectin axis.Epoxyeicosatrienoic acids and heme oxygenase-1 interaction attenuates diabetes and metabolic syndrome complications Plasticity of microvascular oxygenation control in rat fast-twitch muscle: effects of experimental creatine depletion ApoA1: mimetic peptide reverses adipocyte dysfunction in vivo and in vitro via an increase in heme oxygenase (HO-1) and Wnt10b.Valsartan ameliorates ageing-induced aorta degeneration via angiotensin II type 1 receptor-mediated ERK activity Regulation of NAD(P)H oxidases by AMPK in cardiovascular systems AMPKα2 exerts its anti-inflammatory effects through PARP-1 and Bcl-6.AMPK is critical for mitochondrial function during reperfusion after myocardial ischemia.Mitochondria and endothelial function Improved myocardial perfusion in chronic diabetic mice by the up-regulation of pLKB1 and AMPK signaling.The L-4F mimetic peptide prevents insulin resistance through increased levels of HO-1, pAMPK, and pAKT in obese mice Resveratrol induces mitochondrial biogenesis in endothelial cells.α1AMP-activated protein kinase mediates vascular protective effects of exercise.Resveratrol attenuates mitochondrial oxidative stress in coronary arterial endothelial cells.PGC-1α dictates endothelial function through regulation of eNOS expression Chronic Exercise Training Improved Aortic Endothelial and Mitochondrial Function via an AMPKα2-Dependent Manner AMP-activated protein kinase: a stress-responsive kinase with implications for cardiovascular disease.PGC-1 coactivators in cardiac development and disease Vascular endothelium in diabetes.AMP-Activated Protein Kinase: An Ubiquitous Signaling Pathway With Key Roles in the Cardiovascular System.Cardiac macrophage migration inhibitory factor inhibits JNK pathway activation and injury during ischemia/reperfusion

P2860

Q26781354-CD10BD7A-60C7-488C-9AA3-9C920615B3F8 Q26995682-59D37E02-7F4C-44E0-87F8-5BB23DC38350 Q27026657-1B6EEF83-1E89-4184-A6E3-3B128F48C51D Q27320563-E3C0C56C-19B5-4123-AA13-655A0A07B3A5 Q30365745-EE975155-BE80-447A-90CA-530555C66EFF Q33600464-3288969C-34CC-49B9-B496-F7D2D641BFFA Q33769656-D41768FE-7EC9-42A8-A9D5-31CBEE681D04 Q33933093-C00DBACB-1FFE-49F4-B77D-38B1431BCDC5 Q34022332-AC0AE3D9-A6EB-4B7F-95A2-484B7C1EA730 Q34179571-EC67E042-36D2-4B06-A802-3790C58F6582 Q34236772-7C325AC2-3107-4F4D-9979-91E3484105FA Q34236808-8C18E89E-C75C-4406-B316-4485C18CEEE1 Q34502017-62EDF170-7C07-4A30-9265-986145BB6050 Q34518725-8323EC71-B1D9-4E7F-9430-697737FB3D4E Q34540378-6F875C43-2F66-40D5-B763-A13D39DABF61 Q34706435-BDDBFA8C-AAA7-48CC-ADD8-8BD6EEA6BFFE Q34807222-2ACD0630-289F-44E6-88E3-7E66C53C8C32 Q35112954-A38B040A-B842-4DC7-8A3D-48354D04DAEE Q35626960-9CD40F73-EB57-4896-A4BE-886272EFB22C Q35680257-78FF7098-D07E-4C23-BC8D-C996BDB4EA1E Q35681034-AB44836C-7DA2-44F9-8E47-9171E211587C Q35812975-AC90D0D7-71FE-4F08-A81F-34E4A92F66C0 Q35866740-500DAA97-07C3-47D2-80DD-9F91AF698DDD Q35867839-6872145E-DE82-43C4-8165-070DB294E66C Q35925959-71D49BD4-DAB1-4753-84DD-0B772794A47D Q36637370-2AD3A3AF-DF61-4D33-8F4E-B435F8B1CDDE Q36820646-CA6783F3-B067-43AA-81D2-83F074CCE38E Q36979168-3A29B8D6-47E3-4E56-8C5C-99F2C9563C01 Q37045357-68D6DC7A-262D-486A-A35A-28A006680709 Q37222394-07558741-8BF3-445B-A552-CE24EF35E11B Q37264427-515D8091-1ECD-48DF-982A-56789F4B6D64 Q37415163-2D5CD711-EDA9-4E5B-BF2A-1A9B08A5272B Q37430857-B336FE71-8B68-438E-8FCE-2625F96AF7AA Q37464463-BB8790BD-969B-421E-8B19-D49C17E50326 Q37523452-FFEE1396-1AFF-4974-BA84-A080F61712B1 Q37671250-C2DAD19B-8CFF-4DC3-A760-FA08DAF8A73B Q37795417-120ABFA5-B441-4017-8E84-76AAA48FF863 Q39010377-E430541A-B018-4F70-BE21-F4F78D3984AD Q39331294-F960D1EA-25A6-4384-A904-8271FFBAF2DC Q39773528-48FEA2CC-12C1-4553-9F70-8EA6A5E466F8

P2860

Suppression of the JNK pathway by induction of a metabolic stress response prevents vascular injury and dysfunction.

http://www.wikidata.org/entity/Q37372989

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on September 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Suppression of the JNK pathway ...... scular injury and dysfunction.

@en

Suppression of the JNK pathway ...... scular injury and dysfunction.

@nl

type

label

Suppression of the JNK pathway ...... scular injury and dysfunction.

@en

Suppression of the JNK pathway ...... scular injury and dysfunction.

@nl

prefLabel

Suppression of the JNK pathway ...... scular injury and dysfunction.

@en

Suppression of the JNK pathway ...... scular injury and dysfunction.

@nl

P1433

Q37372989-4AAEF276-6852-48A6-BCEF-663CA9109FF9

P1476

Q37372989-172E3FA6-0E62-47CA-BBA1-B7DC61338694

P2093

Q37372989-98CF8929-911B-4526-91CD-630DB3B8CA69

Q37372989-A3720A4E-6501-44C8-8FAA-B69E784F4F7C

Q37372989-AAD62E26-BB50-4BA7-AD4F-733375FE774E

Q37372989-B2AAED8E-4309-4547-BAC3-8D75763BCC14

Q37372989-C6019227-746C-4BDA-831F-712E2549E26C

Q37372989-D8E1DACB-112C-4F64-B23B-78E49447B26B

Q37372989-F269ED1E-6330-41D8-B3C0-B627611B0639

Q37372989-FB3F57DE-5E86-402E-9EF5-C6B0480B959F

P2860

Q37372989-04B522F9-CB41-4229-A32F-30A0BF5C743B

Q37372989-099DEF53-83AE-4887-912F-83B253A66046

Q37372989-0EA8B302-E582-4C21-9A9A-A70F4B8FA551

Q37372989-15F0C4CF-1FDC-4C04-9D83-CF853E33D79C

Q37372989-21C2CFC4-B253-4FFA-85A1-7DF1FF7B117C

Q37372989-22B6DF4F-066E-41D1-A579-11663FED8358

Q37372989-29525816-C484-4F17-9DC6-779E71810E4F

Q37372989-2A7C72A2-7832-40B4-9961-9A1FE88E965D

Q37372989-2AFD882B-B59A-437F-847C-774E52EB4046

Q37372989-2D63B111-B9A2-4D65-BD21-C3761435F724

P304

Q37372989-DBECA5F7-9BC9-4653-B3C7-60C9DE151736

P31

Q37372989-A2F24AD5-AACC-48B5-B75F-3356756E0FC6

P356

Q37372989-D47F1314-797E-48FE-AB08-5122E7879C89

P407

Q37372989-5A1D5F2B-D6EA-4DD8-9EA2-71CB28199607

P433

Q37372989-6090DF43-0C3E-4BAA-BED8-36B39ADC6CBE

P478

Q37372989-A577AF89-6B6E-4D3B-9DA1-3D06D4EAA187

P50

Q37372989-9C75D5A2-B784-4033-828F-0A52271F259C

P577

Q37372989-DF2AF5FA-69D9-45AB-A634-84477BC0116F

P5875

Q37372989-FE4ADDE4-6715-4915-B8E1-4635035D3722

P698

Q37372989-866682F1-34CB-429D-989B-BA8C61E41892

P932

Q37372989-D3E9356D-CC17-4B9E-AC29-835436B61F08

P356

CIRCULATIONAHA.108.784298

P1433

P1476

Suppression of the JNK pathway ...... ascular injury and dysfunction

@en

P2093

Andreas Daiber

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

Eberhard Schulz

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

Jörn Dopheide

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

Kai Chen

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

Philip Wenzel

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

Shane R Thomas

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

Swenja Schuhmacher

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

Thomas Münzel

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

P2860

Role of AMP-activated protein kinase in mechanism of metformin action

AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation.

The AMP-activated protein kinase alpha2 catalytic subunit controls whole-body insulin sensitivity

Control of mitochondrial transcription specificity factors (TFB1M and TFB2M) by nuclear respiratory factors (NRF-1 and NRF-2) and PGC-1 family coactivators

PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis

Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1

Signal transduction by the JNK group of MAP kinases

A role for AMP-activated protein kinase in contraction- and hypoxia-regulated glucose transport in skeletal muscle

Reactive oxygen species promote TNFalpha-induced death and sustained JNK activation by inhibiting MAP kinase phosphatases

The alpha1 and alpha2 isoforms of the AMP-activated protein kinase have similar activities in rat liver but exhibit differences in substrate specificity in vitro

P304

1347-1357

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

P31

scholarly article

P356

10.1161/CIRCULATIONAHA.108.784298

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

P407

P433

13

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

P478

118

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

P50

P577

2008-09-01T00:00:00Z

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

P5875

23272946

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

P698

18809807

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

P932

2756193

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