Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease. - Test2 - elhamkhani - TriplyDB

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease.

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease.

http://www.wikidata.org/entity/Q36320982

about

Control of mitochondrial morphology through differential interactions of mitochondrial fusion and fission proteins An actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2 Identification and characterization of unique proline-rich peptides binding to the mitochondrial fission protein hFis1 Dominant GDAP1 mutations cause predominantly mild CMT phenotypes Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells The mitochondrial outer membrane protein hFis1 regulates mitochondrial morphology and fission through self-interaction New insights into the role of mitochondria in aging: mitochondrial dynamics and more Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H Charcot-Marie-Tooth disease and intracellular traffic The dynamics of the mitochondrial organelle as a potential therapeutic target Dynamin-related protein 1 is required for normal mitochondrial bioenergetic and synaptic function in CA1 hippocampal neurons.The novel F-box protein Mfb1p regulates mitochondrial connectivity and exhibits asymmetric localization in yeast.Mitochondrial fragmentation in neurodegeneration Mitochondrial morphology in metabolic diseases Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy The nuclear genes Mtfr1 and Dufd1 regulate mitochondrial dynamic and cellular respiration Discovery of novel vitamin D-regulated proteins in INS-1 cells: a proteomic approach Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease The PINK1/Parkin pathway regulates mitochondrial morphology Mitochondrial dynamics and apoptosis Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway.Bax/Bak promote sumoylation of DRP1 and its stable association with mitochondria during apoptotic cell death Transgenic control of mitochondrial fission induces mitochondrial uncoupling and relieves diabetic oxidative stress.Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2).Targeting and function of the mitochondrial fission factor GDAP1 are dependent on its tail-anchor.Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome.Small molecule inhibitors of mitochondrial division: tools that translate basic biological research into medicine.Gene expression profiling following short-term and long-term morphine exposure in mice uncovers genes involved in food intake.The neurodegenerative mitochondriopathies.Biophysical properties of mitochondrial fusion events in pancreatic beta-cells and cardiac cells unravel potential control mechanisms of its selectivity.The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan Distinct pathogenic processes between Fig4-deficient motor and sensory neurons.A lethal de novo mutation in the middle domain of the dynamin-related GTPase Drp1 impairs higher order assembly and mitochondrial division.Deceleration of fusion-fission cycles improves mitochondrial quality control during aging.Loss of mitochondrial fission depletes axonal mitochondria in midbrain dopamine neurons.Novel roles for actin in mitochondrial fission SOD1 targeted to the mitochondrial intermembrane space prevents motor neuropathy in the Sod1 knockout mouse.Increased production of reactive oxygen species in hyperglycemic conditions requires dynamic change of mitochondrial morphology.Mitochondrial dynamics in diabetes.Evidence implicating the candidate schizophrenia/bipolar disorder susceptibility gene G72 in mitochondrial function.

P2860

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P2860

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease.

http://www.wikidata.org/entity/Q36320982

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Ganglioside-induced differenti ...... r Charcot-Marie-Tooth disease.

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Ganglioside-induced differenti ...... r Charcot-Marie-Tooth disease.

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P2093

Angelo Schenone

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Axel Niemann

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Marcel Ruegg

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Ueli Suter

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Veronica La Padula

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P2860

Control of mitochondrial morphology by a human mitofusin

GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria

Levels of human Fis1 at the mitochondrial outer membrane regulate mitochondrial morphology

Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins.

Roles of the mammalian mitochondrial fission and fusion mediators Fis1, Drp1, and Opa1 in apoptosis

A human dynamin-related protein controls the distribution of mitochondria

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

Isolation of 10 differentially expressed cDNAs in differentiated Neuro2a cells induced through controlled expression of the GD3 synthase gene

Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene

Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy

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1067-1078

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10.1083/JCB.200507087

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170

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7592001

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16172208

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2171517

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