Related references
Note: Only part of the references are listed.Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders
Serena Carra et al.
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2013)
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins
Serena Carra et al.
PROGRESS IN NEUROBIOLOGY (2012)
Small heat shock proteins, protein degradation and protein aggregation diseases
Michel J. Vos et al.
AUTOPHAGY (2011)
Dysregulation of axonal transport and motorneuron diseases
Daniela Sau et al.
BIOLOGY OF THE CELL (2011)
The emerging role of HSP20 as a multifunctional protective agent
H. V. Edwards et al.
CELLULAR SIGNALLING (2011)
Mechanisms of Compartmental Purkinje Cell Death and Survival in the Lurcher Mutant Mouse
Carol L. Armstrong et al.
CEREBELLUM (2011)
Muscle cells and motoneurons differentially remove mutant SOD1 causing familial amyotrophic lateral sclerosis
Elisa Onesto et al.
JOURNAL OF NEUROCHEMISTRY (2011)
Differential Expression and Induction of Small Heat Shock Proteins in Rat Brain and Cultured Hippocampal Neurons
Britta Bartelt Kirbach et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2011)
17-AAG increases autophagic removal of mutant androgen receptor in spinal and bulbar muscular atrophy
Paola Rusmini et al.
NEUROBIOLOGY OF DISEASE (2011)
A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases
Valeria Crippa et al.
AUTOPHAGY (2010)
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction
Margit Fuchs et al.
BIOCHEMICAL JOURNAL (2010)
The Interaction of αB-Crystallin with Mature α-Synuclein Amyloid Fibrils Inhibits Their Elongation
Christopher A. Waudby et al.
BIOPHYSICAL JOURNAL (2010)
The small heat shock protein, HSPB6, in muscle function and disease
Catherine M. Dreiza et al.
CELL STRESS & CHAPERONES (2010)
Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance
Verena Arndt et al.
CURRENT BIOLOGY (2010)
Small Heat Shock Proteins and Protein-Misfolding Diseases
Ewa Laskowska et al.
CURRENT PHARMACEUTICAL BIOTECHNOLOGY (2010)
Dynamic processes that reflect anti-apoptotic strategies set up by HspB1 (Hsp27)
Catherine Paul et al.
EXPERIMENTAL CELL RESEARCH (2010)
Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice
Margaret Wong et al.
HUMAN MOLECULAR GENETICS (2010)
HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones
Michel J. Vos et al.
HUMAN MOLECULAR GENETICS (2010)
The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS)
Valeria Crippa et al.
HUMAN MOLECULAR GENETICS (2010)
Identification of the Drosophila Ortholog of HSPB8 IMPLICATION OF HSPB8 LOSS OF FUNCTION IN PROTEIN FOLDING DISEASES
Serena Carra et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
The Selective Macroautophagic Degradation of Aggregated Proteins Requires the PI3P-Binding Protein Alfy
Maria Filimonenko et al.
MOLECULAR CELL (2010)
A DNAJB Chaperone Subfamily with HDAC-Dependent Activities Suppresses Toxic Protein Aggregation
Jurre Hageman et al.
MOLECULAR CELL (2010)
Vesicle associated membrane protein B (VAPB) is decreased in ALS spinal cord
Georgia Anagnostou et al.
NEUROBIOLOGY OF AGING (2010)
Small heat-shock proteins interact with a flanking domain to suppress polyglutamine aggregation
Amy L. Robertson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
A novel mutation (F71L) in αA-Crystallin with defective chaperone-like function associated with age-related cataract
S. G. Bhagyalaxmi et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2009)
Transduced HSP27 protein protects neuronal cell death by enhancing FALS-associated SOD1 mutant activity
Jae Jin An et al.
BMB REPORTS (2009)
Blockade of Hsp20 Phosphorylation Exacerbates Cardiac Ischemia/Reperfusion Injury by Suppressed Autophagy and Increased Cell Death
Jiang Qian et al.
CIRCULATION RESEARCH (2009)
Cytoplasmic retention of polyglutamine-expanded androgen receptor ameliorates disease via autophagy in a mouse model of spinal and bulbar muscular atrophy
Heather L. Montie et al.
HUMAN MOLECULAR GENETICS (2009)
γ-Synucleinopathy: neurodegeneration associated with overexpression of the mouse protein
Natalia Ninkina et al.
HUMAN MOLECULAR GENETICS (2009)
HspB8 Participates in Protein Quality Control by a Non-chaperone-like Mechanism That Requires eIF2α Phosphorylation
Serena Carra et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Activation of Gene Transcription by Heat Shock Protein 27 May Contribute to Its Neuronal Protection
Meyer J. Friedman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Structural and functional diversities between members of the human HSPB, HSPH, HSPA, and DNAJ chaperone families
Michel J. Vos et al.
BIOCHEMISTRY (2008)
Skeletal Muscle Is a Primary Target of SOD1G93A-Mediated Toxicity
Gabriella Dobrowolny et al.
CELL METABOLISM (2008)
Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size
Ying Sun et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
Misfolded proteins partition between two distinct quality control compartments
Daniel Kaganovich et al.
NATURE (2008)
Expression of the small heat shock protein family in the mouse CNS: differential anatomical and biochemical compartmentalization
S. Quraishe et al.
NEUROSCIENCE (2008)
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy
Serena Carra et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Monitoring the prevention of amyloid fibril formation by α-crystallin
Agata Rekas et al.
FEBS JOURNAL (2007)
Regulation of stress-induced intracellular sorting and chaperone function of Hsp27 (HspB1) in mammalian cells
Anton L. Bryantsev et al.
BIOCHEMICAL JOURNAL (2007)
Autophagosome formation: Core machinery and adaptations
Zhiping Xie et al.
NATURE CELL BIOLOGY (2007)
Heat-shock protein 105 interacts with and suppresses aggregation of mutant Cu/Zn superoxide dismutase: clues to a possible strategy for treating ALS
Hirofumi Yamashita et al.
JOURNAL OF NEUROCHEMISTRY (2007)
Gene expression analysis of the murine model of amyotrophic lateral sclerosis: Studies of the Leu126delTT mutation in SOD1
Yasuyo Fukada et al.
BRAIN RESEARCH (2007)
Aggregation and proteasome: The case of elongated polyglutamine aggregation in spinal and bulbar muscular atrophy
Paola Rusmini et al.
NEUROBIOLOGY OF AGING (2007)
GFAP and its role in Alexander disease
Roy A. Quinlan et al.
EXPERIMENTAL CELL RESEARCH (2007)
Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activation
Alexandra Zourlidou et al.
HUMAN MOLECULAR GENETICS (2007)
Mechanisms of ataxin-3 misfolding and fibril formation: Kinetic analysis of a disease-associated polyglutamine protein
Andrew M. Ellisdon et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
The small heat shock proteins and their clients
H. Nakamoto et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2007)
Up-regulation of heat shock protein HSP 20 in the hippocampus as an early response to hypoxia of the newborn
Jean-Claude David et al.
JOURNAL OF NEUROCHEMISTRY (2006)
Modulation of Hsp90 function in neurodegenerative disorders: a molecular-targeted therapy against disease-causing protein
Masahiro Waza et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2006)
Onset and progression in inherited ALS determined by motor neurons and microglia
Severine Boillee et al.
SCIENCE (2006)
Alteration of familial ALS-linked mutant SOD1 solubility with disease progression: Its modulation by the proteasome and Hsp70
S Koyama et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Extended polyglutamine tracts cause aggregation and structural perturbation of an adjacent β barrel protein
Z Ignatova et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Specific association of small heat shock proteins with the pathological hallmarks of Alzheimer's disease brains
MMM Wilhelmus et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2006)
Differences in the chaperone-like activities of the four main small heat shock proteins of Drosophila melanogaster
G Morrow et al.
CELL STRESS & CHAPERONES (2006)
Huntingtin and mutant SOD1 form aggregate structures with distinct molecular properties in human cells
G Matsumoto et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Pharmacological induction of heat-shock proteins alleviates polyglutamine-mediated motor neuron disease
M Katsuno et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration
M Waza et al.
NATURE MEDICINE (2005)
Decreased expression of Hsp27 and Hsp70 in transformed lymphoblastoid cells from patients with spinocerebellar ataxia type 7
HF Tsai et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
The role of heat shock proteins Hsp70 and Hsp27 in cellular protection of the central nervous system
TB Franklin et al.
INTERNATIONAL JOURNAL OF HYPERTHERMIA (2005)
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells
S Carra et al.
HUMAN MOLECULAR GENETICS (2005)
Hsp27 and Hsp70 administered in combination have a potent protective effect against FALS-associated SOD1-mutant-induced cell death in mammalian neuronal cells
YJK Patel et al.
MOLECULAR BRAIN RESEARCH (2005)
Hsp27 consolidates intracellular redox homeostasis by upholding glutathione in its reduced form and by decreasing iron intracellular levels
AP Arrigo et al.
ANTIOXIDANTS & REDOX SIGNALING (2005)
HSP27 and cell death in spinocerebellar ataxia type 3
ML Hsieh et al.
CEREBELLUM (2005)
Modulation of neurodegeneration by molecular chaperones
PJ Muchowski et al.
NATURE REVIEWS NEUROSCIENCE (2005)
Testis-specific human small heat shock protein HSPB9 is a cancer/testis antigen, and potentially interacts with the dynein subunit TCTEL1
NJW de Wit et al.
EUROPEAN JOURNAL OF CELL BIOLOGY (2004)
Characterization of the structure and the amyloidogenic properties of the Josephin domain of the polyglutamine-containing protein ataxin-3
L Masino et al.
JOURNAL OF MOLECULAR BIOLOGY (2004)
Interaction of the molecular chaperone αB-crystallin with α-synuclein:: Effects on amyloid fibril formation and chaperone activity
A Rekas et al.
JOURNAL OF MOLECULAR BIOLOGY (2004)
Protein aggregation and neurodegenerative disease
CA Ross et al.
NATURE MEDICINE (2004)
Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice
A Maatkamp et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2004)
Transducible heat shock protein 20 (HSP20) phosphopeptide alters cytoskeletal dynamics
CM Dreiza et al.
FASEB JOURNAL (2004)
Cell biology of protein misfolding: The examples of Alzheimer's and Parkinson's diseases
DJ Selkoe
NATURE CELL BIOLOGY (2004)
Comparison of the small heat shock proteins αB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle
N Golenhofen et al.
HISTOCHEMISTRY AND CELL BIOLOGY (2004)
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
OV Evgrafov et al.
NATURE GENETICS (2004)
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
M Arrasate et al.
NATURE (2004)
Distinct aggregation and cell death patterns among different types of primary neurons induced by mutant huntingtin protein
K Tagawa et al.
JOURNAL OF NEUROCHEMISTRY (2004)
Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein
JP Taylor et al.
HUMAN MOLECULAR GENETICS (2003)
Patterned Purkinje cell degeneration in mouse models of Niemann-Pick type C disease
JR Sarna et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2003)
Upregulation of HSP27 in a transgenic model of ALS
V Vleminckx et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2002)
Hsp27 upregulation and phosphorylation is required for injured sensory and motor neuron survival
SC Benn et al.
NEURON (2002)
Huntington's disease age-of-onset linked to polyglutamine aggregation nucleation
SM Chen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Medicine - The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics
J Hardy et al.
SCIENCE (2002)
Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtin
A Wyttenbach et al.
HUMAN MOLECULAR GENETICS (2002)
Hsp27 as a negative regulator of cytochrome c release
C Paul et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)
Molecular chaperones enhance the degradation of expanded polyglutamine repeat androgen receptor in a cellular model of spinal and bulbar muscular atrophy
CK Bailey et al.
HUMAN MOLECULAR GENETICS (2002)
Crystal structure and assembly of a eukaryotic small heat shock protein
RLM van Montfort et al.
NATURE STRUCTURAL BIOLOGY (2001)
Hsp27: Novel regulator of intracellular redox state
AP Arrigo
IUBMB LIFE (2001)
Differentially expressed genes in rat dorsal root ganglia following peripheral nerve injury
DS Kim et al.
NEUROREPORT (2001)
Protective effect of chaperones on polyglutamine diseases
Y Kobayashi et al.
BRAIN RESEARCH BULLETIN (2001)
Modulation of HSP25 expression during anterior horn motor neuron degeneration in the paralyse mouse mutant
I Pieri et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2001)
Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice
CJ Cummings et al.
HUMAN MOLECULAR GENETICS (2001)
Phosphorylation-induced Change of the Oligomerization state of αB-crystallin
K Ito et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Characterization of α-crystallin-plasma membrane binding
BA Cobb et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Dopaminergic loss and inclusion body formation in α-synuclein mice:: Implications for neurodegenerative disorders
E Masliah et al.
SCIENCE (2000)
Subcellular localization of proteasomes and their regulatory complexes in mammalian cells
P Brooks et al.
BIOCHEMICAL JOURNAL (2000)
Muscle develops a specific form of small heat shock protein complex composed of MKBP/HSPB2 and HSPB3 during myogenic differentiation
Y Sugiyama et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tract
S Simeoni et al.
HUMAN MOLECULAR GENETICS (2000)
Share Paper
