A comparison of the bone and growth phenotype of mdx, mdx:Cmah−/− and mdx:Utrn+/− murine models with the C57BL/10 wild-type mouse

• Үндсэн зохиолчид: Claire L. Wood (Зохиогч), Karla J. Suchacki (Зохиогч), Rob van 't Hof (Зохиогч), Will P. Cawthorn (Зохиогч), Scott Dillon (Зохиогч), Volker Straub (Зохиогч), Sze Choong Wong (Зохиогч), Syed F. Ahmed (Зохиогч), Colin Farquharson (Зохиогч), Annemieke Aartsma-Rus (Зохиогч), James Dowling (Зохиогч), Maaike van Putten (Зохиогч)
• Формат: Ном
• Хэвлэсэн: The Company of Biologists, 2020-02-01T00:00:00Z.
• Нөхцлүүд: article
• Онлайн хандалт: Connect to this object online.

The muscular dystrophy X-linked (mdx) mouse is commonly used as a mouse model of Duchenne muscular dystrophy (DMD). Its phenotype is, however, mild, and other mouse models have been explored. The mdx:Cmah−/− mouse carries a human-like mutation in the Cmah gene and has a severe muscle phenotype, but...