Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells-Reference-Cited by-同舟云学术

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Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells

Published:2022-05-01 Issue:9-10 Volume:31 Page:221-238
ISSN:1547-3287
Container-title:Stem Cells and Development
language:en
Short-container-title:Stem Cells and Development

Author:

Sabitha K. R.¹,Chandran Divya¹,Shetty Ashok K.²³,Upadhya Dinesh¹^ORCID

Affiliation:

1. Centre for Molecular Neurosciences, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.

2. Institute for Regenerative Medicine, Texas A&M University College of Medicine, College Station, Texas, USA.

3. Department of Molecular and Cellular Medicine, Texas A&M University College of Medicine, College Station, Texas, USA.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Developmental Biology,Hematology

Link

https://www.liebertpub.com/doi/pdf/10.1089/scd.2021.0304

Reference172 articles.

1. Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in l-cell fibroblasts

2. An unusual splicing mutation in the HEXB gene is associated with dramatically different phenotypes in patients from different racial backgrounds.

3. Niemann-Pick C1 protein: Obligatory roles for N-terminal domains and lysosomal targeting in cholesterol mobilization

4. Autophagy fights disease through cellular self-digestion

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Infantile spasms caused by NEXMIF mutation: A case report and literature review;Applied Neuropsychology: Child;2023-06-14

2. Neurological Disease Modeling Using Pluripotent and Multipotent Stem Cells: A Key Step towards Understanding and Treating Mucopolysaccharidoses;Biomedicines;2023-04-21

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