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Cold Spring Harbor Perspectives in Medicine|August 22, 2012
The ubiquitin-proteasome system and the autophagic-lysosomal system in Alzheimer diseaseYasuo Ihara, Maho Morishima-Kawashima, Ralph NixonJournal of Human Evolution|July 10, 2020
A demographic test of accidental versus intentional island colonization by Pleistocene humansYasuo Ihara, Kazunobu Ikeya, Atsushi Nobayashi, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|May 3, 2021
Childcare support and child social development in Japan: investigating the mediating role of parental psychological condition and parenting styleMasahito Morita, Atsuko Saito, Mari Nozaki, et al.The Journal of Biological Chemistry|November 21, 2007
Abeta46 is processed to Abeta40 and Abeta43, but not to Abeta42, in the low density membrane domainsSosuke Yagishita, Maho Morishima-Kawashima, Shoichi Ishiura, et al.Journal of Neurochemistry|December 30, 2016
Alanine substitutions in the GXXXG motif alter C99 cleavage by γ-secretase but not its dimerizationHidekazu Higashide, Seiko Ishihara, Mika Nobuhara, et al.Neurobiology of Aging|October 13, 2012
Suspected limited efficacy of γ-secretase modulatorsNobuto Kakuda, Kohei Akazawa, Hiroyuki Hatsuta, et al.Biochemistry|January 29, 2003
Distinct mechanisms by mutant presenilin 1 and 2 leading to increased intracellular levels of amyloid beta-protein 42 in Chinese hamster ovary cellsYue Qi, Maho Morishima-Kawashima, Toru Sato, et al.Theoretical Population Biology|June 15, 2023
Cultural niche construction with application to fertility control: A model for education and social transmission of contraceptive useKaleda K Denton, Jeremy R Kendal, Yasuo Ihara, et al.Biochemistry|March 22, 2006
DAPT-induced intracellular accumulations of longer amyloid beta-proteins: further implications for the mechanism of intramembrane cleavage by gamma-secretaseSousuke Yagishita, Maho Morishima-Kawashima, Yu Tanimura, et al.Translational Psychiatry|November 3, 2021
Switched Aβ43 generation in familial Alzheimer's disease with presenilin 1 mutationNobuto Kakuda, Mako Takami, Masayasu Okochi, et al.Pageof 10