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Search references for HSPB8. Phrases containing HSPB8
See searches and references containing HSPB8!HSPB8
shock protein beta-8 is a protein that in humans is encoded by the HSPB8 gene. HSPB8 has been shown to interact with: HSPB2, and Hsp27. Mutations in this
HSPB8
Protein found in the eye
THBP 314 HSPB2_HUMAN HSPB2 182 HSPB3_HUMAN HSPB3 HSP27 HSPL27 150 HSPB8_HUMAN HSPB8 CRYAC E2IG1 HSP22 PP1629 196 HSPB7_HUMAN HSPB7 CVHSP 170 HSPB9_HUMAN
Crystallin
selective autophagy complex comprises the molecular chaperones HSPA8 and HSPB8, and the cochaperones BAG3 and STUB1. The cochaperone BAG3 plays a vital
Chaperone-assisted selective autophagy
Chaperone-assisted_selective_autophagy
Protein-coding gene in the species Homo sapiens
encoded by the HSPB2 gene. HSPB2 has been shown to interact with: CRYAB, HSPB8, Myotonic dystrophy protein kinase and TRAF6. GRCh38: Ensembl release 89:
HSPB2
22q11.2 D 1:4,000 Distal hereditary motor neuropathies, multiple types HSPB8, HSPB1, HSPB3, GARS, REEP1, IGHMBP2, SLC5A7, DCTN1, TRPV4, SIGMAR1 Distal
List_of_genetic_disorders
Protein-coding gene in the species Homo sapiens
Fontaine JM, Sun X, Benndorf R, Welsh MJ (2005). "Interactions of HSP22 (HSPB8) with HSP20, alphaB-crystallin, and HSPB3". Biochem. Biophys. Res. Commun
HSPB6
Protein family
greatly affected. HSPB1 HSPB2 HSPB3 HSPB4 (CRYAA) HSPB5 (CRYAB) HSPB6 HSPB7 HSPB8 HSPB9 HSPB10 Lindquist S, Craig EA (1988). "The heat-shock proteins". Annu
Hsp20
Brain activity monitoring technique
Wuyts, Charlotte; Sisto, Angela; Pintelon, Isabel; et al. (16 May 2022). "HSPB8-enriched extracellular vesicles from oligodendroglia are protective against
Photoencephalography
Protein-coding gene in the species Homo sapiens
JM, Sun X, Benndorf R, Welsh MJ (November 2005). "Interactions of HSP22 (HSPB8) with HSP20, alphaB-crystallin, and HSPB3". Biochemical and Biophysical
HSPB3
Protein-coding gene in the species Homo sapiens
been shown to interact with: ASK1, CIMIP6, CRYAA, CRYAB, CRYBB2, HNRPD, HSPB8, MK2, TAK1, and TGFB1I1. GRCh38: Ensembl release 89: ENSG00000106211 – Ensembl
Hsp27
Peripheral nervous system disorders
GDAP1 8q21.11 Autosomal dominant Allelic with subtype CMT2H CMT2L 608673 HSPB8 12q24.23 Autosomal dominant Allelic with Autosomal dominant distal spinal
Charcot–Marie–Tooth disease classifications
Charcot–Marie–Tooth_disease_classifications
Protein found in humans
In muscle cells, BAG3 cooperates with the molecular chaperones Hsc70 and HspB8 to induce the degradation of mechanically damaged cytoskeleton components
BAG3
Group of motor neuron diseases
dominant juvenile distal spinal muscular atrophy Juvenile onset DHMN2A 158590 HSPB8 12q24.23 Autosomal dominant Autosomal dominant distal spinal muscular atrophy
Distal hereditary motor neuronopathies
Distal_hereditary_motor_neuronopathies
Q12988 7333 HSPB6 HGNC:26511; O14558 7334 HSPB7 HGNC:5249; Q9UBY9 7335 HSPB8 HGNC:30171; Q9UJY1 7336 HSPB9 HGNC:30589; Q9BQS6 7337 HSPBAP1 HGNC:16389;
List of human protein-coding genes 4
List_of_human_protein-coding_genes_4
Muscular degenerative disorders caused by dysfunction of spinal neurons
muscular atrophy Distal hereditary motor neuronopathy type 2A (DHMN2A) 158590 HSPB8 12q24.23 Autosomal dominant Adult-onset. Allelic with Charcot–Marie–Tooth
Spinal_muscular_atrophies
Cytoplasmic biomolecular condensates of proteins and RNA occurring in cells under stress
Poser I, Lee HO, et al. (September 2016). "A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism"
Stress_granule
Histopathologist
C, Zelotti E, Baratashvili M, Gregory JM, et al. (2016). The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects
Jenna_Gregory
2K; 607831; GDAP1 Charcot–Marie–Tooth disease, axonal, type 2L; 608673; HSPB8 Charcot–Marie–Tooth disease, axonal, type 2M; 606482; DNM2 Charcot–Marie–Tooth
List_of_OMIM_disorder_codes
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