Crossmark

Mutation-induced loss of APP function causes GABAergic depletion in recessive familial Alzheimer’s disease: analysis of Osaka mutation-knockin mice

Crossref DOI link: https://doi.org/10.1186/s40478-017-0461-5

Published Online: 2017-07-31

Published Print: 2017-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Umeda, Tomohiro

Kimura, Tetsuya

Yoshida, Kayo

Takao, Keizo

Fujita, Yuki

Matsuyama, Shogo

Sakai, Ayumi

Yamashita, Minato

Yamashita, Yuki

Ohnishi, Kiyouhisa

Suzuki, Mamiko

Takuma, Hiroshi

Miyakawa, Tsuyoshi

Takashima, Akihiko

Morita, Takashi

Mori, Hiroshi

Tomiyama, Takami https://orcid.org/0000-0001-6040-0178
Funding

Funding for this research was provided by:

Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (20023026, 21390271, 23110514, 25290018, 16K15132)

Grant-in-Aid for Scientific Research on Innovative Areas (Comprehensive Brain Science Network) from the Ministry of Education, Culture, Sports, Science and Technology of Japan

Grants-in-Aid for Comprehensive Research on Dementia from the Ministry of Health, Labour, and Welfare, Japan

Alzheimer’s Association (IIRG-09-132098)