Artikel: A novel HSPB1
Prostaglandins & other lipid mediators
2023 Band 169, Seite(n) 106769
Abstract: Charcot-Marie-Tooth Disease (CMT) is a commonly inherited peripheral polyneuropathy. Clinical manifestations for this disease include symmetrical distal polyneuropathy, altered deep tendon reflexes, distal sensory loss, foot deformities, and gait ... ...
Abstract | Charcot-Marie-Tooth Disease (CMT) is a commonly inherited peripheral polyneuropathy. Clinical manifestations for this disease include symmetrical distal polyneuropathy, altered deep tendon reflexes, distal sensory loss, foot deformities, and gait abnormalities. Genetic mutations in heat shock proteins have been linked to CMT2. Specifically, mutations in the heat shock protein B1 (HSPB1) gene encoding for heat shock protein 27 (Hsp27) have been linked to CMT2F and distal hereditary motor and sensory neuropathy type 2B (dHMSN2B) subtype. The goal of the study was to examine the role of an endogenous mutation in HSPB1 in vivo and to define the effects of this mutation on motor function and pathology in a novel animal model. As sphingolipids have been implicated in hereditary and sensory neuropathies, we examined sphingolipid metabolism in central and peripheral nervous tissues in 3-month-old Hsp |
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Mesh-Begriff(e) | Mice ; Animals ; Charcot-Marie-Tooth Disease/genetics ; Charcot-Marie-Tooth Disease/pathology ; Heat-Shock Proteins/genetics ; Mutation/genetics ; Disease Models, Animal ; Sphingolipids | |||||
Chemische Substanzen | Heat-Shock Proteins ; Sphingolipids | |||||
Sprache | Englisch | |||||
Erscheinungsdatum | 2023-08-23 | |||||
Erscheinungsland | United States | |||||
Dokumenttyp | Journal Article ; Research Support, N.I.H., Extramural | |||||
ZDB-ID | 1426962-4 | |||||
ISSN | 2212-196X ; 1098-8823 ; 0090-6980 | |||||
ISSN (online) | 2212-196X | |||||
ISSN | 1098-8823 ; 0090-6980 | |||||
DOI | 10.1016/j.prostaglandins.2023.106769 | |||||
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Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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