α‐Galactosidase A‐deficient rats accumulate glycosphingolipids and develop cardiorenal phenotypes of Fabry disease-Reference-Cited by-同舟云学术

α‐Galactosidase A‐deficient rats accumulate glycosphingolipids and develop cardiorenal phenotypes of Fabry disease

Published:2018-07-06 Issue:1 Volume:33 Page:418-429
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Miller James J.¹,Aoki Kazuhiro¹,Mascari Carly A.¹,Beltrame Angela K.¹,Sokumbi Olayemi²,North Paula E.³,Tiemeyer Michael⁴,Kriegel Alison J.¹,Dahms Nancy M.⁵

Affiliation:

1. Department of PhysiologyMedical College of Wisconsin Milwaukee Wisconsin USA

2. Department of DermatologyMedical College of Wisconsin Milwaukee Wisconsin USA

3. Department of PathologyMedical College of Wisconsin Milwaukee Wisconsin USA

4. Complex Carbohydrate Research CenterUniversity of Georgia Athens Georgia USA

5. Department of BiochemistryMedical College of Wisconsin Milwaukee Wisconsin USA

Funder

National Institutes of Health

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute of Neurological Disorders and Stroke

National Institute of Allergy and Infectious Diseases

National Institute of General Medical Sciences

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.201800771R

Reference48 articles.

1. The lysosome turns fifty

2. The awesome lysosome

3. Sphingolipid lysosomal storage disorders

4. Fabry disease

5. Fabry Disease: Preclinical Studies Demonstrate the Effectiveness of α-Galactosidase A Replacement in Enzyme-Deficient Mice

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