Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Receptors, Ectodysplasin/metabolism"'
Autor:
Del-Pozo, Jorge, Macintyre, Neil, Anvari Azar, Ali, Headon, Denis, Schneider, Pascal, Cheeseman, Michael
Publikováno v:
Disease models & mechanisms, vol. 12, no. 4
Disease Models & Mechanisms, Vol 12, Iss 4 (2019)
Disease Models & Mechanisms
Del-Pozo, J, Macintyre, N, Anvari Azar, A, Headon, D, Schneider, P & Cheeseman, M 2019, ' Role of Ectodysplasin signalling in middle ear and nasal pathology in rat and mouse models of hypohidrotic ectodermal dysplasia ', Disease Models and Mechanisms, vol. 12, no. 4, dmm037804 . https://doi.org/10.1242/dmm.037804
Disease Models & Mechanisms, Vol 12, Iss 4 (2019)
Disease Models & Mechanisms
Del-Pozo, J, Macintyre, N, Anvari Azar, A, Headon, D, Schneider, P & Cheeseman, M 2019, ' Role of Ectodysplasin signalling in middle ear and nasal pathology in rat and mouse models of hypohidrotic ectodermal dysplasia ', Disease Models and Mechanisms, vol. 12, no. 4, dmm037804 . https://doi.org/10.1242/dmm.037804
Patients with mutations in the ectodysplasin receptor signalling pathway genes – the X-linked ligand ectodysplasin-A (EDA), the receptor EDAR or the receptor adapter EDARADD – have hypohidrotic ectodermal dysplasia (HED). In addition to having im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8a0f6a56e671c696ffe35395a899b92b
https://serval.unil.ch/resource/serval:BIB_4103E7371D49.P001/REF.pdf
https://serval.unil.ch/resource/serval:BIB_4103E7371D49.P001/REF.pdf
Autor:
Laure Willen, Pascal Schneider, Aubry Tardivel, Manuel Favre, Lee Kim Swee, Stéphane Demotz, Marja L. Mikkola, Karine Ingold-Salamin, Olivier Gaide
Publikováno v:
J Biol Chem
Journal of Biological Chemistry, Vol. 284, No 40 (2009) pp. 27567-27576
Journal of Biological Chemistry, vol. 284, no. 40, pp. 27567-27576
Journal of Biological Chemistry, Vol. 284, No 40 (2009) pp. 27567-27576
Journal of Biological Chemistry, vol. 284, no. 40, pp. 27567-27576
Mutations in the TNF family ligand EDA1 cause X-linked hypohidrotic ectodermal dysplasia (XLHED), a condition characterized by defective development of skin appendages. The EDA1 protein displays a proteolytic processing site responsible for its conve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::068d6b13c26388b5d6b70474d33524c2
https://europepmc.org/articles/PMC2785685/
https://europepmc.org/articles/PMC2785685/