Cargando…
Hypersensitivity of myelinated A-fibers via toll-like receptor 5 promotes mechanical allodynia in tenascin-X-deficient mice associated with Ehlers–Danlos syndrome
Deficiency of an extracellular matrix glycoprotein tenascin-X (TNX) leads to a human heritable disorder Ehlers–Danlos syndrome, and TNX-deficient patients complain of chronic joint pain, myalgia, paresthesia, and axonal polyneuropathy. We previously reported that TNX-deficient (Tnxb(−/−)) mice exhib...
Autores principales: | Kamada, Hiroki, Emura, Kousuke, Yamamoto, Rikuto, Kawahara, Koichi, Uto, Sadahito, Minami, Toshiaki, Ito, Seiji, Matsumoto, Ken-ichi, Okuda-Ashitaka, Emiko |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613304/ https://www.ncbi.nlm.nih.gov/pubmed/37898719 http://dx.doi.org/10.1038/s41598-023-45638-7 |
Ejemplares similares
-
Mechanical allodynia in mice with tenascin-X deficiency associated with Ehlers-Danlos syndrome
por: Okuda-Ashitaka, Emiko, et al.
Publicado: (2020) -
Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
por: Okuda-Ashitaka, Emiko, et al.
Publicado: (2023) -
Recurrent pneumothorax in a case of tenascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum
por: Santoreneos, Renee, et al.
Publicado: (2022) -
Ehlers-Danlos syndrome
por: Taj, Farhana Tahseen, et al.
Publicado: (2014) -
Visceroptosis and the Ehlers-Danlos Syndrome
por: Kucera, Stephen, et al.
Publicado: (2017)