MRI detects early hindlimb muscle atrophy in Gly93Ala superoxide dismutase-1 (G93A SOD1) transgenic mice, an animal model of familial amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

MRI detects early hindlimb muscle atrophy in Gly93Ala superoxide dismutase-1 (G93A SOD1) transgenic mice, an animal model of familial amyotrophic lateral sclerosis

Published:2004-02 Issue:1 Volume:17 Page:28-32
ISSN:0952-3480
Container-title:NMR in Biomedicine
language:en
Short-container-title:NMR Biomed.

Author:

Brooks Keith J.,Hill Mark D. W.,Hockings Paul D.,Reid David G.

Publisher

Wiley

Subject

Spectroscopy,Radiology Nuclear Medicine and imaging,Molecular Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/nbm.861/fullpdf

Reference24 articles.

1. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis;Rosen;Nature,1993

2. Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions;Tu;Proc. Natl. Acad. Sci. USA,1996

3. The use of transgenic mouse models of amyotrophic lateral sclerosis in preclinical drug studies;Gurney;J. Neurol. Sci.,1997

4. Animal models of ALS;Pioro;Clin. Neurosci.,1995

5. Familial amyotrophic lateral sclerosis and Alzheimer's disease. Transgenic models;Wong;Adv. Exp. Med. Biol.,1998

Cited by 33 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. Skeletal myotubes expressing ALS mutant SOD1 induce pathogenic changes, impair mitochondrial axonal transport, and trigger motoneuron death;2024-05-26

2. Integrative genetic and single cell RNA sequencing analysis provides new clues to the amyotrophic lateral sclerosis neurodegeneration;Frontiers in Neuroscience;2023-02-17

3. MyomiRs and their multifaceted regulatory roles in muscle homeostasis and amyotrophic lateral sclerosis;Journal of Cell Science;2021-06-15

4. Effects of vitamin E on neurodegenerative diseases: an update;Acta Neurobiologiae Experimentalis;2021

5. Impairment Mechanisms and Intervention Approaches for Aged Human Neuromuscular Junctions;Frontiers in Molecular Neuroscience;2020-11-16