The neuronal retromer can regulate both neuronal and microglial phenotypes of Alzheimer's disease-Reference-Cited by-同舟云学术

The neuronal retromer can regulate both neuronal and microglial phenotypes of Alzheimer's disease

Published:2022-01 Issue:3 Volume:38 Page:110262
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Qureshi Yasir H.^ORCID,Berman Diego E.,Marsh Samuel E.,Klein Ronald L.,Patel Vivek M.^ORCID,Simoes Sabrina,Kannan Suvarnambiga,Petsko Gregory A.^ORCID,Stevens Beth,Small Scott A.

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference96 articles.

1. Über eine eigenartige Erkrankung der Hirnrinde. “A Characteristic Disease of the Cerebral Cortex”;Alzheimer;Neurologisches Centralblatt,1906

2. Über eine eigenartige Erkrankung der Hirnrinde. , 64, 146-148.;Alzheimer;Allgemeine Zeitschrift fur Psychiatrie und Psychisch-gerichtliche Medizin,1907

3. Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms;Andorfer;J. Neurochem.,2003

4. Analysis of transduction efficiency, tropism and axonal transport of AAV serotypes 1, 2, 5, 6, 8 and 9 in the mouse brain;Aschauer;PLoS One,2013

5. A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer's disease;Barthelemy;Nat. Med.,2020

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