Effects of mutations and deletions in the human optineurin gene. - Wikidata - wikimedia - TriplyDB

Effects of mutations and deletions in the human optineurin gene.

Effects of mutations and deletions in the human optineurin gene.

http://www.wikidata.org/entity/Q37668615

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Impaired Autophagy and Defective Mitochondrial Function: Converging Paths on the Road to Motor Neuron Degeneration Functional analysis of optineurin and some of its disease-associated mutants A Glaucoma-Associated Variant of Optineurin, M98K, Activates Tbk1 to Enhance Autophagosome Formation and Retinal Cell Death Dependent on Ser177 Phosphorylation of Optineurin Induction of autophagy in rats upon overexpression of wild-type and mutant optineurin gene.An integrative systems genetics approach reveals potential causal genes and pathways related to obesity.Identification of an Alu-repeat-mediated deletion of OPTN upstream region in a patient with a complex ocular phenotype.Optineurin: The autophagy connection.Stepwise Differentiation of Retinal Ganglion Cells from Human Pluripotent Stem Cells Enables Analysis of Glaucomatous Neurodegeneration.Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosis.Optineurin: A Coordinator of Membrane-Associated Cargo Trafficking and Autophagy.Altered Functions and Interactions of Glaucoma-Associated Mutants of Optineurin.

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Effects of mutations and deletions in the human optineurin gene.

http://www.wikidata.org/entity/Q37668615

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 19 February 2014

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Effects of mutations and deletions in the human optineurin gene.

@en

Effects of mutations and deletions in the human optineurin gene.

@nl

type

label

Effects of mutations and deletions in the human optineurin gene.

@en

Effects of mutations and deletions in the human optineurin gene.

@nl

prefLabel

Effects of mutations and deletions in the human optineurin gene.

@en

Effects of mutations and deletions in the human optineurin gene.

@nl

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Effects of mutations and deletions in the human optineurin gene

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Beatrice Yjt Yue

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Hongyu Ying

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Sanja Turturro

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Xiang Shen

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P2860

Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis

Optineurin negatively regulates the induction of IFNbeta in response to RNA virus infection

Phosphorylation of the autophagy receptor optineurin restricts Salmonella growth

Interaction of an adenovirus E3 14.7-kilodalton protein with a novel tumor necrosis factor alpha-inducible cellular protein containing leucine zipper domains

Differential effects of myocilin and optineurin, two glaucoma genes, on neurite outgrowth

Optineurin negatively regulates TNFalpha- induced NF-kappaB activation by competing with NEMO for ubiquitinated RIP

Current understanding of conventional outflow dysfunction in glaucoma

Posttranslational modifications, localization, and protein interactions of optineurin, the product of a glaucoma gene

FIP-2, a coiled-coil protein, links Huntingtin to Rab8 and modulates cellular morphogenesis

Phorbol esters and cytokines regulate the expression of the NEMO-related protein, a molecule involved in a NF-kappa B-independent pathway

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10.1186/2193-1801-3-99

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Rajalekshmy Shyam

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