Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases.
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HSPB1, HSPB6, HSPB7 and HSPB8 protect against RhoA GTPase-induced remodeling in tachypaced atrial myocytesChaperonopathies: Spotlight on Hereditary Motor NeuropathiesCombined Gene Expression and RNAi Screening to Identify Alkylation Damage Survival Pathways from Fly to HumanAxonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel MutationsThe aggregation and neurotoxicity of TDP-43 and its ALS-associated 25 kDa fragment are differentially affected by molecular chaperones in Drosophila.Granulostasis: Protein Quality Control of RNP Granules.Molecular mechanisms used by chaperones to reduce the toxicity of aberrant protein oligomers.Small heat shock proteins and α-crystallins: dynamic proteins with flexible functions.Specific protein homeostatic functions of small heat-shock proteins increase lifespan.Coordinate regulation of eIF2α phosphorylation by PPP1R15 and GCN2 is required during Drosophila development.The 5'-3' exoribonuclease Pacman (Xrn1) regulates expression of the heat shock protein Hsp67Bc and the microRNA miR-277-3p in Drosophila wing imaginal discs.The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity.The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells.Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders.Contribution of small heat shock proteins to muscle development and function.Barcoding heat shock proteins to human diseases: looking beyond the heat shock responseOverexpression of cystathionine γ-lyase suppresses detrimental effects of spinocerebellar ataxia type 3.Molecular chaperones and neuronal proteostasis.A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8.Molecular Characterization of Six Small Heat Shock Proteins and Their Responses Under Cadmium Stress in Oxya chinensis (Orthoptera: Acridoidea).An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8.BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch.Novel insights in the disease biology of mutant small heat shock proteins in neuromuscular diseases.HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes.
P2860
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P2860
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases.
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Identification of the Drosophi ...... n in protein folding diseases.
@ast
Identification of the Drosophi ...... n in protein folding diseases.
@en
Identification of the Drosophi ...... n in protein folding diseases.
@nl
type
label
Identification of the Drosophi ...... n in protein folding diseases.
@ast
Identification of the Drosophi ...... n in protein folding diseases.
@en
Identification of the Drosophi ...... n in protein folding diseases.
@nl
prefLabel
Identification of the Drosophi ...... n in protein folding diseases.
@ast
Identification of the Drosophi ...... n in protein folding diseases.
@en
Identification of the Drosophi ...... n in protein folding diseases.
@nl
P2093
P2860
P50
P356
P1476
Identification of the Drosophi ...... on in protein folding diseases
@en
P2093
Alessandra Boncoraglio
Bart Kanon
Jeanette F Brunsting
Kay Seidel
Ody C M Sibon
P2860
P304
37811-37822
P356
10.1074/JBC.M110.127498
P407
P577
2010-09-21T00:00:00Z