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  4. Characterisation of the pathophysiology of neuropathy and sensory dysfunction in a mouse model of recessive dystrophic epidermolysis bullosa
Details

Characterisation of the pathophysiology of neuropathy and sensory dysfunction in a mouse model of recessive dystrophic epidermolysis bullosa

Journal
Pain
ISSN
0304-3959
1872-6623
Date Issued
2022
Author(s)
Daniela Schmidt
Paula Díaz
Daniela Muñoz
Fernanda Espinoza
Alexander Nystrom
FUENTES BUSTOS, MARIA IGNACIA  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
EZQUER, EDUARDO MARCELO  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
David L. Bennett
Margarita Calvo
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85138450868
WoS ID
WOS:000854379700021
DOI
10.1097/j.pain.0000000000002599
URL
https://investigadores.udd.cl/handle/123456789/5346
URL Institutional Repository
https://repositorio.udd.cl/handle/11447/7453
Cite this document
Schmidt, D., Díaz, P., Muñoz, D., Espinoza, F., Nystrom, A., Fuentes, I., Ezquer, M., Bennett, D. L., & Calvo, M. (2022). Characterisation of the pathophysiology of neuropathy and sensory dysfunction in a mouse model of recessive dystrophic epidermolysis bullosa. Pain, 163(10), 2052-2060. https://doi.org/10.1097/j.pain.0000000000002599
Subjects
mouse model

; 

neuropathic pain

; 

neuropathy

; 

rdeb

; 

small-fibre neuropathy

; 

animals

; 

collagen type vii

; 

disease models, animal

; 

epidermolysis bullosa dystrophica

; 

humans

; 

mice

; 

mutation

; 

skin

; 

small fiber neuropathy

; 

activating transcription factor 3

; 

calcitonin gene related peptide

; 

collagen type 7

; 

col7a1 protein, human

; 

collagen type 7

; 

adult

; 

animal experiment

; 

animal model

; 

animal tissue

; 

article

; 

astrocyte

; 

axonal injury

; 

c57bl 6 mouse

; 

cell population

; 

controlled study

; 

epidermolysis bullosa dystrophica

; 

female

; 

glia cell

; 

heat sensitivity

; 

hind paw

; 

hyposensitivity (sensory dysfunction)

; 

macrophage

; 

male

; 

mechanical hyperalgesia

; 

microglia

; 

morphology

; 

mouse

; 

mouse model

; 

myelinated nerve

; 

nerve ending

; 

nerve fiber

; 

nerve fiber c

; 

nerve fiber degeneration

; 

nervous system inflammation

; 

neuropathy

; 

nociception

; 

nonhuman

; 

nonmyelinated nerve

; 

pain receptor

; 

pathophysiology

; 

place preference

; 

recessive inheritance

; 

satellite glial cell

; 

scratching

; 

sensory dysfunction

; 

sensory nerve cell

; 

somatosensory system

; 

spinal cord nerve cell

; 

spinal ganglion

; 

thermal hyperalgesia

; 

animal

; 

complication

; 

disease model

; 

genetics

; 

human

; 

metabolism

; 

mutation

; 

pathology

; 

skin

; 

small fiber neuropathy
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