Mechanical allodynia in mice with tenascin-X deficiency associated with Ehlers-Danlos syndrome

Tenascin-X (TNX) is a member of the extracellular matrix glycoprotein tenascin family, and TNX deficiency leads to Ehlers-Danlos syndrome, a heritable human disorder characterized mostly by skin hyperextensibility, joint hypermobility, and easy bruising. TNX-deficient patients complain of chronic jo...

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Detalles Bibliográficos
Autores principales: Okuda-Ashitaka, Emiko, Kakuchi, Yuka, Kakumoto, Hiroaki, Yamanishi, Shota, Kamada, Hiroki, Yoshidu, Takafumi, Matsukawa, Satoshi, Ogura, Naoya, Uto, Sadahito, Minami, Toshiaki, Ito, Seiji, Matsumoto, Ken-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162960/
https://www.ncbi.nlm.nih.gov/pubmed/32300146
http://dx.doi.org/10.1038/s41598-020-63499-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162960/
https://www.ncbi.nlm.nih.gov/pubmed/32300146
http://dx.doi.org/10.1038/s41598-020-63499-2

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