Croll, Susan D.,Ikiz, Burcin,Lacroix-Fralish, Michael
申请号：
AU2016233250
公开号：
AU2016233250A1
申请日:
2016.03.16
申请国别(地区):
AU
年份:
2017
代理人:
摘要：
An animal model for motor neuron dysfunction in disease, e.g., amyotrophic lateral sclerosis (ALS), comprising a genetically modified non-human animal that comprises a genetically modified DR6 allele and exhibits normal phenotypes at birth and for a few weeks or months after birth. However, as the non-human animal ages, it develops motor neuron dysfunction that presents as one or more ALS-like symptoms, which may progress rapidly after onset. Methods of identifying candidate agents that may be used to prevent, delay or treat ALS are also provided.
