Hereditary inclusion body myopathy: single patient response to GNE gene Lipoplex therapy-Reference-Cited by-同舟云学术

Hereditary inclusion body myopathy: single patient response to GNE gene Lipoplex therapy

Published:2010-03-30 Issue:5 Volume:12 Page:403-412
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J. Gene Med.

Author:

Nemunaitis Gregory,Maples Phillip B.,Jay Chris,Gahl William A.,Huizing Marjan,Poling Justin,Tong Alex W.,Phadke Anagha P.,Pappen Beena O.,Bedell Cynthia,Templeton Nancy S.,Kuhn Joseph,Senzer Neil,Nemunaitis John

Publisher

Wiley

Subject

Genetics(clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Reference50 articles.

1. New advances in inclusion-body myositis;Askanas;Curr Opin Rheumatol,1993

2. Review: hereditary inclusion body myopathy (HIBM2);Jay;Gene Regul Syst Biol,2009

3. A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase;Hinderlich;J Biol Chem,1997

4. Disease mechanisms associated with mutations of the GNE gene;Huizing;Drug Discov Today Dis Mech,2005

5. Sialic acids as ligands in recognition phenomena;Varki;FASEB J,1997

Cited by 23 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. Non-viral delivery of nucleic acid for treatment of rare diseases of the muscle;Journal of Biosciences;2024-02-16

2. GNE Myopathy;Current Clinical Neurology;2023

3. A phase 3 randomized study evaluating sialic acid extended-release for GNE myopathy;Neurology;2019-01-25

4. Fighting the Cause of Alzheimer’s and GNE Myopathy;Frontiers in Neuroscience;2018-10-15

5. GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges;Neurotherapeutics;2018-10