A tecpr2 knockout mouse exhibits age-dependent neuroaxonal dystrophy associated with autophagosome accumulation-Reference-Cited by-同舟云学术

A tecpr2 knockout mouse exhibits age-dependent neuroaxonal dystrophy associated with autophagosome accumulation

Published:2020-12-10 Issue:10 Volume:17 Page:3082-3095
ISSN:1554-8627
Container-title:Autophagy
language:en
Short-container-title:Autophagy

Author:

Tamim-Yecheskel Bat-Chen¹,Fraiberg Milana¹,Kokabi Kamilya¹,Freud Saskia¹,Shatz Oren¹,Marvaldi Letizia¹^ORCID,Subic Nemanja¹,Brenner Ori²^ORCID,Tsoory Michael²,Eilam-Altstadter Raya²,Biton Inbal²,Savidor Alon³^ORCID,Dezorella Nili⁴,Heimer Gali⁵⁶,Behrends Christian⁷^ORCID,Ben-Zeev Bruria⁵⁶,Elazar Zvulun¹

Affiliation:

1. Departments of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot, Israel

2. Veterinary Recourses, The Weizmann Institute of Science, Rehovot, Israel

3. Chemical Research Support, The Weizmann Institute of Science, Rehovot, Israel

4. Irving and Cherna Moskowitz Center for Nano and Bio-Nano Imaging, The Weizmann Institute of Science, Rehovot, Israel

5. Department of Pediatric Neurology Unit, Edmond and Lilly Safra Children Hospital, Chaim Sheba Medical Center, Ramat Gan, Israel

6. Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel

7. Munich Cluster for Systems Neurology (Synergy), Ludwig-Maximilians-Universität München, München, Germany

Funder

Deutsche Forschungsgemeinschaft

H2020 Marie Skłodowska-Curie Actions

Israel Science Foundation

Collaborative Research Center 1177

Publisher

Informa UK Limited

Subject

Cell Biology,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15548627.2020.1852724

Reference40 articles.

1. Cloning and Characterization of Physarum polycephalumTectonins

2. Human Genome and Diseases:¶WD-repeat proteins: structure characteristics, biological function, and their involvement in human diseases

3. TECPR2 Cooperates with LC3C to Regulate COPII-Dependent ER Export

4. Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis

5. TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability

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