Iminosugar C ‐Glycosides Work as Pharmacological Chaperones of NAGLU, a Glycosidase Involved in MPS IIIB Rare Disease**-Reference-Cited by-同舟云学术

Iminosugar C ‐Glycosides Work as Pharmacological Chaperones of NAGLU, a Glycosidase Involved in MPS IIIB Rare Disease**

Published:2021-07-02 Issue:44 Volume:27 Page:11291-11297
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Zhu Sha¹,Jagadeesh Yerri²,Tran Anh Tuan¹,Imaeda Shuki³,Boraston Alisdair⁴^ORCID,Alonzi Dominic S.⁵,Poveda Ana⁶^ORCID,Zhang Yongmin¹,Désiré Jérôme²^ORCID,Charollais‐Thoenig Julie⁷,Demotz Stéphane⁷,Kato Atsushi³^ORCID,Butters Terry D.⁵,Jiménez‐Barbero Jesús⁶^ORCID,Sollogoub Matthieu¹^ORCID,Blériot Yves²^ORCID

Affiliation:

1. Sorbonne Université CNRS, Institut Parisien de Chimie Moléculaire UMR 8232 4 place Jussieu 75005 Paris France

2. Glycochemistry Group of “OrgaSynth” Team IC2MP, UMR-CNRS 7285 Université de Poitiers 4 rue Michel Brunet 86073 Poitiers Cedex 9 France

3. Department of Hospital Pharmacy University of Toyama 2630 Sugitani Toyama 930-0194 Japan

4. Department of Biochemistry and Microbiology University of Victoria P.O. Box 3055, Station CSC V8W 3P6 Victoria BC Canada

5. Oxford Glycobiology Institute University of Oxford South Parks Road Oxford OX1 3QU U.K.

6. CIC bioGUNE Bizkaia Technological Park, Building 801A-1° 48160 Derio-Bizkaia Spain

7. Dorphan SA, EPFL Innovation Park 1015 Lausanne Switzerland

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202101408

Reference49 articles.

1. Sanfilippo syndrome: A mini-review

2. Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical, and biological implications

3. Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy

4. How close are we to therapies for Sanfilippo disease?

5. Enzyme Replacement Therapy: A Review and Its Role in Treating Lysosomal Storage Diseases

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