Dymple, a novel dynamin-like high molecular weight GTPase lacking a proline-rich carboxyl-terminal domain in mammalian cells
about
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28Identification of a novel kinesin-related protein, KRMP1, as a target for mitotic peptidyl-prolyl isomerase Pin1Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cellsThe dynamin-like GTPase DLP1 is essential for peroxisome division and is recruited to peroxisomes in part by PEX11SUMOylation of the mitochondrial fission protein Drp1 occurs at multiple nonconsensus sites within the B domain and is linked to its activity cycleRecruitment of an alternatively spliced form of synaptojanin 2 to mitochondria by the interaction with the PDZ domain of a mitochondrial outer membrane protein.PEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferationA human dynamin-related protein controls the distribution of mitochondriaComposition and dynamics of human mitochondrial nucleoidsThe dynamin-related GTPase, Dnm1p, controls mitochondrial morphology in yeastMitochondria-specific function of the dynamin family protein DLP1 is mediated by its C-terminal domainsA proline-rich region and nearby cysteine residues target XLalphas to the Golgi complex regionMammalian dynamin-like protein DLP1 tubulates membranes.A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.Mitochondrial dynamics in diabetes.Dynamin-related protein 1 as a therapeutic target in cardiac arrestRedundant and distinct functions for dynamin-1 and dynamin-2 isoforms.Dynamin-like protein 1 reduction underlies mitochondrial morphology and distribution abnormalities in fibroblasts from sporadic Alzheimer's disease patients.The dynamin-like protein DLP1 is essential for normal distribution and morphology of the endoplasmic reticulum and mitochondria in mammalian cells.A functional interplay between the small GTPase Rab11a and mitochondria-shaping proteins regulates mitochondrial positioning and polarization of the actin cytoskeleton downstream of Src family kinases.Mechanisms of mitochondrial fission and fusion.Dysfunctional mitochondrial fission impairs cell reprogrammingDrp1 mediates caspase-independent type III cell death in normal and leukemic cellsIntra- and intermolecular domain interactions of the C-terminal GTPase effector domain of the multimeric dynamin-like GTPase Drp1.The ever-growing complexity of the mitochondrial fission machinery.
P2860
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P2860
Dymple, a novel dynamin-like high molecular weight GTPase lacking a proline-rich carboxyl-terminal domain in mammalian cells
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@ast
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@en
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@nl
type
label
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@ast
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@en
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@nl
prefLabel
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@ast
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@en
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@nl
P2093
P2860
P356
P1476
Dymple, a novel dynamin-like h ...... inal domain in mammalian cells
@en
P2093
P2860
P304
P356
10.1074/JBC.273.2.1044
P407
P577
1998-01-09T00:00:00Z