Correcting mitochondrial fusion by manipulating mitofusin conformations. - Wikidata - wikimedia - TriplyDB

Correcting mitochondrial fusion by manipulating mitofusin conformations.

Correcting mitochondrial fusion by manipulating mitofusin conformations.

http://www.wikidata.org/entity/Q30839081

about

MFN1 structures reveal nucleotide-triggered dimerization critical for mitochondrial fusion Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression.Connecting mitochondrial dynamics and life-or-death events via Bcl-2 family proteins.Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.Mitochondria-Associated Membranes As Networking Platforms and Regulators of Cancer Cell Fate.A membrane-inserted structural model of the yeast mitofusin Fzo1.Dosis Facit Sanitatem-Concentration-Dependent Effects of Resveratrol on Mitochondria.Mitophagy as a Protective Mechanism against Myocardial Stress.Transit and integration of extracellular mitochondria in human heart cells.Sequences flanking the transmembrane segments facilitate mitochondrial localization and membrane fusion by mitofusin.A new mitofusin topology places the redox-regulated C terminus in the mitochondrial intermembrane space.A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A family.Structure, function, and regulation of mitofusin-2 in health and disease.Regulation of mitochondrial bioenergetics by the non-canonical roles of mitochondrial dynamics proteins in the heart.The ever-growing complexity of the mitochondrial fission machinery.Judging a tumor cell by its cover: a matter of mitochondrial contact sites.The INs and OUTs of mitofusins.Abrogating Mitochondrial Dynamics in Mouse Hearts Accelerates Mitochondrial Senescence.GRK2 moderates the acute mitochondrial damage to ionizing radiation exposure by promoting mitochondrial fission/fusion.Redox crosstalk at endoplasmic reticulum (ER) membrane contact sites (MCS) uses toxic waste to deliver messages.MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A.The heptad repeat domain 1 of Mitofusin has membrane destabilization function in mitochondrial fusion.Mitofusin 2: from functions to disease.Structural basis for membrane tethering by a bacterial dynamin-like pair

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P2860

Correcting mitochondrial fusion by manipulating mitofusin conformations.

http://www.wikidata.org/entity/Q30839081

description

2016 nî lūn-bûn

@nan

2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

Correcting mitochondrial fusion by manipulating mitofusin conformations.

@ast

Correcting mitochondrial fusion by manipulating mitofusin conformations.

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type

label

Correcting mitochondrial fusion by manipulating mitofusin conformations.

@ast

Correcting mitochondrial fusion by manipulating mitofusin conformations.

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prefLabel

Correcting mitochondrial fusion by manipulating mitofusin conformations.

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Correcting mitochondrial fusion by manipulating mitofusin conformations.

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P1476

Correcting mitochondrial fusion by manipulating mitofusin conformations.

@en

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Ann Benz

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

Antonietta Franco

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

Daria Mochly-Rosen

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

Gerald W Dorn

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

Guohua Gong

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

Julie A Fleischer

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

Nikolaos Biris

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

Nir Qvit

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

Opher S Kornfeld

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

Richard N Kitsis

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

P2860

Control of mitochondrial morphology through differential interactions of mitochondrial fusion and fission proteins

PINK1-phosphorylated mitofusin 2 is a Parkin receptor for culling damaged mitochondria

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

Disruption of fusion results in mitochondrial heterogeneity and dysfunction

The I-TASSER Suite: protein structure and function prediction.

Trans-mitochondrial coordination of cristae at regulated membrane junctions.

Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.

Mitochondrial fission and fusion factors reciprocally orchestrate mitophagic culling in mouse hearts and cultured fibroblasts

Loss of Local Astrocyte Support Disrupts Action Potential Propagation and Glutamate Release Synchrony from Unmyelinated Hippocampal Axon Terminals In Vitro

Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations.

P2888

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74-79

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scholarly article

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10.1038/NATURE20156

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P433

7631

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540

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Evripidis Gavathiotis

Sara K Donnelly

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2016-10-24T00:00:00Z

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1033654667

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27775718

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5315023

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