Behavioral profile in a Dctn1G71A knock-in mouse model of Perry disease
Author:
Funder
Japan Society for the Promotion of Science
Ministry of Health, Labour and Welfare
Publisher
Elsevier BV
Subject
General Neuroscience
Reference24 articles.
1. Hereditary mental depression and Parkinsonism with taurine deficiency;Perry;Arch. Neurol.,1975
2. Japanese family with parkinsonism, depression, weight loss, and central hypoventilation;Tsuboi;Neurology,2002
3. DCTN1 mutations in Perry syndrome;Farrer;Nat. Genet.,2009
4. Establishing diagnostic criteria for Perry syndrome;Mishima;J. Neurol. Neurosurg. Psychiatry,2018
5. Novel destabilizing Dynactin variant (DCTN1 p.Tyr78His) in patient with Perry syndrome;Cierny;Parkinsonism Relat. Disord.,2020
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1. Dysregulation of stress granule dynamics by DCTN1 deficiency exacerbates TDP-43 pathology in Drosophila models of ALS/FTD;Acta Neuropathologica Communications;2024-02-04
2. Perry Disease: Bench to Bedside Circulation and a Team Approach;Biomedicines;2024-01-05
3. Ninjinyoeito Prevents Onset of Depression-Like Behavior and Reduces Hippocampal iNOS Expression in Senescence-Accelerated Mouse Prone 8 Mice;Evidence-Based Complementary and Alternative Medicine;2023-08-09
4. Deficiency of Perry syndrome-associated p150Glued in midbrain dopaminergic neurons leads to progressive neurodegeneration and endoplasmic reticulum abnormalities;npj Parkinson's Disease;2023-03-07
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