Property of Lysosomal Storage Disease Associated with Midbrain Pathology in the Central Nervous System of Lamp-2–Deficient Mice-Reference-Cited by-同舟云学术

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Property of Lysosomal Storage Disease Associated with Midbrain Pathology in the Central Nervous System of Lamp-2–Deficient Mice

Published:2015-06 Issue:6 Volume:185 Page:1713-1723
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Furuta Akiko,Kikuchi Hisae,Fujita Hiromi,Yamada Daisuke,Fujiwara Yuuki,Kabuta Tomohiro,Nishino Ichizo,Wada Keiji,Uchiyama Yasuo

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology

National Institute of Biomedical Innovation

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference35 articles.

1. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease);Nishino;Nature,2000

2. Lysosomal glycogen storage disease with normal acid maltase;Danon;Neurology,1981

3. Autophagic vacuolar myopathies;Nishino;Curr Neurol Neurosci Rep,2003

4. Autophagic vacuoles with sarcolemmal features delineate Danon disease and related myopathies;Sugie;J Neuropathol Exp Neurol,2005

5. Lysosomal storage and advanced senescence in the brain of LAMP-2-deficient Danon disease;Furuta;Acta Neuropathol,2013

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1. Lamp1 Deficiency Enhances Sensitivity to α-Synuclein and Oxidative Stress in Drosophila Models of Parkinson Disease;International Journal of Molecular Sciences;2022-10-28

2. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1;Autophagy;2021-01-02

3. Ataxic phenotype and neurodegeneration are triggered by the impairment of chaperone‐mediated autophagy in cerebellar neurons;Neuropathology and Applied Neurobiology;2020-08-09

4. A Nationwide Survey on Danon Disease in Japan;International Journal of Molecular Sciences;2018-11-08

5. Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice;The American Journal of Pathology;2016-12

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