Charcot-Marie-Tooth Hereditary Neuropathy Overview. PMID: 20301532
The roles of HSP40/DNAJ protein family in neurodegenerative diseases. PMID: 36581576
DNAJB2-related Charcot-Marie-Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening. PMID: 35286755
Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation. PMID: 33369814
DNAJB2 expression in normal and diseased human and mouse skeletal muscle. PMID: 20395441
The heat shock protein DNAJB2 as a novel biomarker for essential thrombocythemia diagnosis associated with immune infiltration. PMID: 36746103
Chaperonopathies: Spotlight on Hereditary Motor Neuropathies. PMID: 28018906
DNAJB2 c.184C>T mutation associated with distal hereditary motor neuropathy with rimmed vacuolar myopathy. PMID: 35652544
Extension of the DNAJB2a isoform in a dominant neuromyopathy family. PMID: 37070754
Protein kinase CK2 modulates HSJ1 function through phosphorylation of the UIM2 domain. PMID: 28031292
Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism. PMID: 27449489
Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results. PMID: 32093037
Charcot-Marie-Tooth Neuropathy Type 2 – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. PMID: 20301462
Genetic Analysis of HSP40/DNAJ Family Genes in Parkinson's Disease: a Large Case-Control Study. PMID: 35715682
Huntington's disease: fighting on many fronts. PMID: 22427330
[Genetic distribution in Chinese patients with hereditary peripheral neuropathy]. PMID: 36241230
Allosteric heat shock protein 70 inhibitors rapidly rescue synaptic plasticity deficits by reducing aberrant tau. PMID: 23607970
Mitochondrial dynamics and inherited peripheral nerve diseases. PMID: 25847151
Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy. PMID: 26752306
Suppression of protein aggregation by chaperone modification of high molecular weight complexes. PMID: 22396390
Gene expression profiling in human skeletal muscle during recovery from eccentric exercise. PMID: 18321953
Identification and characterization of a human mitochondrial homologue of the bacterial co-chaperone GrpE. PMID: 11311562
Molecular analysis and clinical diversity of distal hereditary motor neuropathy. PMID: 32298515
A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation. PMID: 22522442
Co-chaperone HSJ1a dually regulates the proteasomal degradation of ataxin-3. PMID: 21625540
PolyQ-expanded proteins impair cellular proteostasis of ataxin-3 through sequestering the co-chaperone HSJ1 into aggregates. PMID: 33837238
Differential recognition of heat-shock protein dnaJ-derived epitopes by effector and Treg cells leads to modulation of inflammation in juvenile idiopathic arthritis. PMID: 17469159
Differences in Circulating microRNAs between Grazing and Grain-Fed Wagyu Cattle Are Associated with Altered Expression of Intramuscular microRNA, the Potential Target PTEN, and Lipogenic Genes. PMID: 27611783
HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrum. PMID: 25274842
Screening of hub genes and prediction of putative drugs in arsenic-related bladder carcinoma: An in silico study. PMID: 32663744
The expression of oxidative stress genes related to myocardial ischemia reperfusion injury in patients with ST-elevation myocardial infarction. PMID: 35237363
The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease. PMID: 34169998
Molecular chaperone-mediated rescue of mitophagy by a Parkin RING1 domain mutant. PMID: 20889486
Interaction of the human DnaJ homologue, HSJ1b with the 90 kDa heat shock protein, Hsp90. PMID: 10983842
Versatile members of the DNAJ family show Hsp70 dependent anti-aggregation activity on RING1 mutant parkin C289G. PMID: 27713507
Molecular chaperone mediated late-stage neuroprotection in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis. PMID: 24023695
HSJ1 is a neuronal shuttling factor for the sorting of chaperone clients to the proteasome. PMID: 15936278
Analysis of the role of ubiquitin-interacting motifs in ubiquitin binding and ubiquitylation. PMID: 15155768
The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosis. PMID: 26936937
Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase. PMID: 16604191
Neuronal DnaJ proteins HSJ1a and HSJ1b: a role in linking the Hsp70 chaperone machine to the ubiquitin-proteasome system? PMID: 15270696
Impact of Heat Stress on Cellular and Transcriptional Adaptation of Mammary Epithelial Cells in Riverine Buffalo (Bubalus Bubalis). PMID: 27682256
The chaperone environment at the cytoplasmic face of the endoplasmic reticulum can modulate rhodopsin processing and inclusion formation. PMID: 12754272
Assignment of the neuronal cochaperone, HSJ1, to human chromosome bands 2q32-->q34 between D2S295 and D2S339 by in situ hybridization and somatic cell and radiation hybrids. PMID: 10516435
Impaired DNAJB2 Response to Heat Shock in Fibroblasts from a Neuropathy Patient with DNAJB2/HSJ1 Mutation: Cystamine as a Potential Therapeutic Intervention., PMID:40423229
DNAJB2 Attenuates Rosacea Skin Inflammation and Angiogenesis by Inhibiting the Endoplasmic Reticulum Stress-mediated TLR2/Myd88/NF-κB pathway., PMID:40035989
Polymorphism in Genes Encoding HSP40 Family Proteins is Associated with Ischemic Stroke Risk and Brain Infarct Size: A Pilot Study., PMID:39735968
Effects of treadmill exercise on endoplasmic reticulum protein folding and endoplasmic reticulum-associated protein degradation pathways in APP/PS1 mice., PMID:39397952
Extension of the DNAJB2a isoform in a dominant neuromyopathy family., PMID:37070754
The heat shock protein DNAJB2 as a novel biomarker for essential thrombocythemia diagnosis associated with immune infiltration., PMID:36746103
The roles of HSP40/DNAJ protein family in neurodegenerative diseases., PMID:36581576
[Genetic distribution in Chinese patients with hereditary peripheral neuropathy]., PMID:36241230
Genetic Analysis of HSP40/DNAJ Family Genes in Parkinson's Disease: a Large Case-Control Study., PMID:35715682
DNAJB2 c.184C>T mutation associated with distal hereditary motor neuropathy with rimmed vacuolar myopathy., PMID:35652544
DNAJB2-related Charcot-Marie-Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening., PMID:35286755
The expression of oxidative stress genes related to myocardial ischemia reperfusion injury in patients with ST-elevation myocardial infarction., PMID:35237363
The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease., PMID:34169998
PolyQ-expanded proteins impair cellular proteostasis of ataxin-3 through sequestering the co-chaperone HSJ1 into aggregates., PMID:33837238
Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation., PMID:33369814
Screening of hub genes and prediction of putative drugs in arsenic-related bladder carcinoma: An in silico study., PMID:32663744
Molecular analysis and clinical diversity of distal hereditary motor neuropathy., PMID:32298515
Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results., PMID:32093037
Protein kinase CK2 modulates HSJ1 function through phosphorylation of the UIM2 domain., PMID:28031292
Chaperonopathies: Spotlight on Hereditary Motor Neuropathies., PMID:28018906
Versatile members of the DNAJ family show Hsp70 dependent anti-aggregation activity on RING1 mutant parkin C289G., PMID:27713507
Impact of Heat Stress on Cellular and Transcriptional Adaptation of Mammary Epithelial Cells in Riverine Buffalo (Bubalus Bubalis)., PMID:27682256
Differences in Circulating microRNAs between Grazing and Grain-Fed Wagyu Cattle Are Associated with Altered Expression of Intramuscular microRNA, the Potential Target PTEN, and Lipogenic Genes., PMID:27611783
Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism., PMID:27449489
The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosis., PMID:26936937
Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy., PMID:26752306
Mitochondrial dynamics and inherited peripheral nerve diseases., PMID:25847151
HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrum., PMID:25274842
Molecular chaperone mediated late-stage neuroprotection in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis., PMID:24023695
Allosteric heat shock protein 70 inhibitors rapidly rescue synaptic plasticity deficits by reducing aberrant tau., PMID:23607970
A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation., PMID:22522442
Huntington's disease: fighting on many fronts., PMID:22427330
Suppression of protein aggregation by chaperone modification of high molecular weight complexes., PMID:22396390
Co-chaperone HSJ1a dually regulates the proteasomal degradation of ataxin-3., PMID:21625540
Molecular chaperone-mediated rescue of mitophagy by a Parkin RING1 domain mutant., PMID:20889486
DNAJB2 expression in normal and diseased human and mouse skeletal muscle., PMID:20395441
Gene expression profiling in human skeletal muscle during recovery from eccentric exercise., PMID:18321953
Differential recognition of heat-shock protein dnaJ-derived epitopes by effector and Treg cells leads to modulation of inflammation in juvenile idiopathic arthritis., PMID:17469159
Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase., PMID:16604191
HSJ1 is a neuronal shuttling factor for the sorting of chaperone clients to the proteasome., PMID:15936278
Neuronal DnaJ proteins HSJ1a and HSJ1b: a role in linking the Hsp70 chaperone machine to the ubiquitin-proteasome system?, PMID:15270696
Analysis of the role of ubiquitin-interacting motifs in ubiquitin binding and ubiquitylation., PMID:15155768
The chaperone environment at the cytoplasmic face of the endoplasmic reticulum can modulate rhodopsin processing and inclusion formation., PMID:12754272
Identification and characterization of a human mitochondrial homologue of the bacterial co-chaperone GrpE., PMID:11311562
Interaction of the human DnaJ homologue, HSJ1b with the 90 kDa heat shock protein, Hsp90., PMID:10983842
Assignment of the neuronal cochaperone, HSJ1, to human chromosome bands 2q32-->q34 between D2S295 and D2S339 by in situ hybridization and somatic cell and radiation hybrids., PMID:10516435
For research use only. Not for human or drug use.
