Chemical Therapies for Congenital Disorders of Glycosylation-Reference-Cited by-同舟云学术

Chemical Therapies for Congenital Disorders of Glycosylation

Published:2021-11-17 Issue: Volume: Page:
ISSN:1554-8929
Container-title:ACS Chemical Biology
language:en
Short-container-title:ACS Chem. Biol.

Author:

Sosicka Paulina¹,Ng Bobby G.¹,Freeze Hudson H.¹^ORCID

Affiliation:

1. Human Genetics Program, Sanford Children’s Health Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, United States

Funder

National Institute of Neurological Disorders and Stroke

National Institute of Diabetes and Digestive and Kidney Diseases

Rocket Fund

Publisher

American Chemical Society (ACS)

Subject

Molecular Medicine,General Medicine,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acschembio.1c00601

Reference69 articles.

1. Perspectives on Glycosylation and Its Congenital Disorders

2. Neurological Aspects of Human Glycosylation Disorders

3. Congenital Disorders of Glycosylation

4. Drug screens of NGLY1 Deficiency worm and fly models reveal catecholamine, NRF2 and anti-inflammatory pathway activation as potential clinical approaches

5. Repurposing the aldose reductase inhibitor and diabetic neuropathy drug epalrestat for the congenital disorder of glycosylation PMM2-CDG

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1. Identification of two novel variants in ALG11 causing congenital disorder of glycosylation;Seizure: European Journal of Epilepsy;2024-10

2. Genome and RNA sequencing were essential to reveal cryptic intronic variants associated to defective ATP6AP1 mRNA processing;Molecular Genetics and Metabolism;2024-07

3. Glycosphingolipids in congenital disorders of glycosylation (CDG);Molecular Genetics and Metabolism;2024-05

4. Protein glycosylation and glycoinformatics for novel biomarker discovery in neurodegenerative diseases;Ageing Research Reviews;2023-08

5. Complex metabolic disharmony in PMM2-CDG paves the way to new therapeutic approaches;Molecular Genetics and Metabolism;2023-07