标题
Insights on Human Small Heat Shock Proteins and Their Alterations in Diseases
作者
关键词
-
出版物
Frontiers in Molecular Biosciences
Volume 9, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2022-02-25
DOI
10.3389/fmolb.2022.842149
参考文献
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- Infantile muscular dystrophy in Canadian aboriginals is an αB-crystallinopathy
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- Expression of Two Testis-specific Genes, SPATA19 and LEMD1, in Prostate Cancer
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- Activation of the unfolded protein response by a cataract-associated αA-crystallin mutation
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- Effects of congenital cataract mutation R116H on αA-crystallin structure, function and stability
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- The Interaction of αB-Crystallin with Mature α-Synuclein Amyloid Fibrils Inhibits Their Elongation
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- Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3)
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- Common Variants in HSPB7 and FRMD4B Associated With Advanced Heart Failure
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- Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance
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- Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation
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- Dynamic processes that reflect anti-apoptotic strategies set up by HspB1 (Hsp27)
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- Independent evolution of the core domain and its flanking sequences in small heat shock proteins
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- Mutant HSPB8 causes motor neuron-specific neurite degeneration
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- HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones
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- The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS)
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- Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy
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- Identification of theDrosophilaOrtholog of HSPB8
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- Selective degradation of aggregate-prone CryAB mutants by HSPB1 is mediated by ubiquitin–proteasome pathways
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- Small heat shock protein 20 (HspB6) in cardiac hypertrophy and failure
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- Proteomic profiling of x-linked muscular dystrophy
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- Molecular characterization of rat cvHsp/HspB7 in vitro and its dynamic molecular architecture
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- Mutant small heat shock protein B3 causes motor neuropathy: Utility of a candidate gene approach
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- The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy
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- Infantile onset myofibrillar myopathy due to recessive CRYAB mutations
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- Detection and Architecture of Small Heat Shock Protein Monomers
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- Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy
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- Identification of the key structural motifs involved in HspB8/HspB6–Bag3 interaction
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- HSPB7 is a SC35 speckle resident small heat shock protein
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- The pivotal role of the β7 strand in the intersubunit contacts of different human small heat shock proteins
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- Why proteins without an α-crystallin domain should not be included in the human small heat shock protein family HSPB
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- Blockade of Hsp20 Phosphorylation Exacerbates Cardiac Ischemia/Reperfusion Injury by Suppressed Autophagy and Increased Cell Death
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- Protein quality control during aging involves recruitment of the macroautophagy pathway by BAG3
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- Suppression of GFAP toxicity by αB-crystallin in mouse models of Alexander disease
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- Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease
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- The Small Heat-Shock Proteins HSPB2 and HSPB3 Form Well-defined Heterooligomers in a Unique 3 to 1 Subunit Ratio
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- Proteomic profiling of antisense-induced exon skipping reveals reversal of pathobiochemical abnormalities in dystrophic mdx diaphragm
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- Mutation in BAG3 causes severe dominant childhood muscular dystrophy
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- Mechanism of Insolubilization by a Single-Point Mutation in αA-Crystallin Linked with Hereditary Human Cataracts†
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- Abnormal Assemblies and Subunit Exchange of αB-Crystallin R120 Mutants Could Be Associated with Destabilization of the Dimeric Substructure†
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- Cataract mutation P20S of αB-crystallin impairs chaperone activity of αA-crystallin and induces apoptosis of human lens epithelial cells
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- Heterooligomeric complexes formed by human small heat shock proteins HspB1 (Hsp27) and HspB6 (Hsp20)
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- Evidence that a Protein Kinase A Substrate, Small Heat-Shock Protein 20, Modulates Myometrial Relaxation in Human Pregnancy
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- On the mechanism of organelle degradation in the vertebrate lens
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- Human Mutation in the Anti-apoptotic Heat Shock Protein 20 Abrogates Its Cardioprotective Effects
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- HspB8 Participates in Protein Quality Control by a Non-chaperone-like Mechanism That Requires eIF2α Phosphorylation
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- Truncation of αB-Crystallin by the Myopathy-causing Q151X Mutation Significantly Destabilizes the Protein Leading to Aggregate Formation in Transfected Cells
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- Asymmetrical late onset motor neuropathy associated with a novel mutation in the small heat shock protein HSPB1 (HSP27)
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- Autophagy is an adaptive response in desmin-related cardiomyopathy
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- The small heat shock-related protein, HSP20, is a cAMP-dependent protein kinase substrate that is involved in airway smooth muscle relaxation
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- Unmasking different mechanical and energetic roles for the small heat shock proteins CryAB and HSPB2 using genetically modified mouse hearts
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