Impaired autophagy affects acid α-glucosidase processing and enzyme replacement therapy efficacy in late-onset glycogen storage disease type II-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Impaired autophagy affects acid α-glucosidase processing and enzyme replacement therapy efficacy in late-onset glycogen storage disease type II

Published:2015-05-02 Issue:5 Volume:41 Page:672-675
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Nascimbeni Anna Chiara¹,Fanin Marina¹,Tasca Elisabetta²,Angelini Corrado¹²,Sandri Marco³⁴

Affiliation:

1. Department of Neurosciences; University of Padova; Padova Italy

2. Fondazione IRCCS San Camillo Hospital; Venice Italy

3. Dulbecco Telethon Institute at Venetian Institute of Molecular Medicine; Padova Italy

4. Department of Biomedical Science; University of Padova; Padova Italy

Funder

AFM

Telethon-Italy

Eurobiobank network

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Reference8 articles.

1. The value of muscle biopsies in Pompe disease: identifying lipofucsin inclusions in juvenile- and adult-onset patients;Feeney;Acta Neuropathol Commun,2014

2. When more is less: excess and deficiency of autophagy coexist in skeletal muscle in Pompe disease;Raben;Autophagy,2009

3. The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII);Nascimbeni;Cell Death Differ,2012

4. Autophagy is required to maintain muscle mass;Masiero;Cell Metab,2009

Cited by 34 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. Lentiviral gene therapy with IGF2-tagged GAA normalizes the skeletal muscle proteome in murine Pompe disease;Journal of Proteomics;2024-01

2. Increasing Enzyme Mannose-6-Phosphate Levels but Not Miglustat Coadministration Enhances the Efficacy of Enzyme Replacement Therapy in Pompe Mice;Journal of Pharmacology and Experimental Therapeutics;2023-09-07

3. Screening data from 19 patients with late‐onset Pompe disease for a phase I clinical trial of AAV8 vector‐mediated gene therapy;JIMD Reports;2023-08-17

4. Clinical Advances in Neuromuscular Diseases: Neurometabolic Disorders;Muscles;2023-07-17

5. Screening chimeric GAA variants in preclinical study results in hematopoietic stem cell gene therapy candidate vectors for Pompe disease;Molecular Therapy - Methods & Clinical Development;2022-12

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3