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Presenilin-1 Knockin Mice Reveal Loss-of-Function Mechanism for Familial Alzheimer’s Disease

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Year: 2015
Type: article
Source: Neuron
DOI: 10.1016/j.neuron.2015.02.010
Authors: Dan Xia, Hirotaka Watanabe, Bei Wu, Sang Hun Lee, Yan Li, Evgeny Tsvetkov, Vadim Y. Bolshakov, Jie Shen, Raymond J. Kelleher
Institutions: Brigham and Women's Hospital, Harvard University, Massachusetts General Hospital, McLean Hospital
Language: English

Topic: Alzheimer's disease research and treatments
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: bronze

Funder: National Institute of Neurological Disorders and Stroke
Awards: Mechanisms of brain phenotypes caused by FAD-linked Presenilin-1 Mutations, Presenilin and APP in the Brain, APP/APLP1/APLP2 in the brain, Presenilin and APP in the Brain
OpenAlex ID: W2024024756
FWCI: 22.11
Cites: 56
Cited by: 228
Related to: 10
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