Cln1 ‐mutations suppress Rab7‐RILP interaction and impair autophagy contributing to neuropathology in a mouse model of infantile neuronal ceroid lipofuscinosis-Reference-Cited by-同舟云学术

Cln1 ‐mutations suppress Rab7‐RILP interaction and impair autophagy contributing to neuropathology in a mouse model of infantile neuronal ceroid lipofuscinosis

Published:2020-04-27 Issue:5 Volume:43 Page:1082-1101
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:Jrnl of Inher Metab Disea

Author:

Sarkar Chinmoy¹²,Sadhukhan Tamal¹,Bagh Maria B.¹,Appu Abhilash P.¹,Chandra Goutam¹³,Mondal Avisek¹,Saha Arjun¹⁴,Mukherjee Anil B.¹^ORCID

Affiliation:

1. Section on Developmental Genetics, Division of Translational Medicine Eunice Kennedy Shriver National Institute of Child Health and Human Development Bethesda Maryland USA

2. Department of Anesthesiology University of Maryland School of Medicine 655 West Baltimore Street, MSTF # 6‐00, Baltimore MD USA

3. Center for Development and Aging Research, Inter University Center for Biomedical Research & Super Specialty Hospital Mahatma Gandhi University Campus at Thalappady Kottayam Kerala India

4. Robertson Clinical and Translational Cell Therapy Program, Marcus Center for Cellular Cures Duke University School of Medicine Chesterfield Building, Room 5413, 701 W Main Street, Durham NC USA

Funder

National Institutes of Health

National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12242

Reference57 articles.

1. Autophagy: from phenomenology to molecular understanding in less than a decade

2. Autophagy pathway: Cellular and molecular mechanisms