Preselective gene therapy for Fabry disease-Reference-Cited by-同舟云学术

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Preselective gene therapy for Fabry disease

Published:2001-03-06 Issue:6 Volume:98 Page:3428-3433
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Qin G.,Takenaka T.,Telsch K.,Kelley L.,Howard T.,Levade T.,Deans R.,Howard B. H.,Malech H. L.,Brady R. O.,Medin J. A.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference31 articles.

1. Targeting of Proteins to the Lysosome

2. Correction in trans for Fabry disease: expression, secretion and uptake of alpha-galactosidase A in patient-derived cells driven by a high-titer recombinant retroviral vector.

3. Infusion of alpha -galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease

4. -Galactosidase A deficient mice: A model of Fabry disease

Cited by 63 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. Anderson–Fabry disease management: role of the cardiologist;European Heart Journal;2024-03-15

2. Lysosomal storage diseases. Sphingolipidoses — Fabry, Gaucher and Farber diseases;Pediatrician (St. Petersburg);2022-07-09

3. Ion channels and pain in Fabry disease;Molecular Pain;2021-01

4. Lessons from iPSC research: Insights on peripheral nerve disease;Neuroscience Letters;2020-11

5. Fabry disease: α-galactosidase A deficiency;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

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