ATF3 expression improves motor function in the ALS mouse model by promoting motor neuron survival and retaining muscle innervation-Reference-Cited by-同舟云学术

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ATF3 expression improves motor function in the ALS mouse model by promoting motor neuron survival and retaining muscle innervation

Published:2014-01-13 Issue:4 Volume:111 Page:1622-1627
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:

Seijffers R.,Zhang J.,Matthews J. C.,Chen A.,Tamrazian E.,Babaniyi O.,Selig M.,Hynynen M.,Woolf C. J.,Brown R. H.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference46 articles.

1. Molecular biology of amyotrophic lateral sclerosis: insights from genetics

2. Amyotrophic lateral sclerosis

3. Current hypotheses for the underlying biology of amyotrophic lateral sclerosis

4. Rethinking ALS: The FUS about TDP-43

5. UNRAVELING THE MECHANISMS INVOLVED IN MOTOR NEURON DEGENERATION IN ALS

Cited by 53 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. AAV-NRIP gene therapy ameliorates motor neuron degeneration and muscle atrophy in ALS model mice;Skeletal Muscle;2024-07-24

2. SUMOylation of nuclear receptor Nor1/NR4A3 coordinates microtubule cytoskeletal dynamics and stability in neuronal cells;Cell & Bioscience;2024-07-13

3. ATF3 is a neuron‐specific biomarker for spinal cord injury and ischaemic stroke;Clinical and Translational Medicine;2024-04

4. Transcriptional modulation unique to vulnerable motor neurons predicts ALS across species and SOD1 mutations;2024-03-17

5. Selective vulnerability of motor neuron types and functional groups to degeneration in amyotrophic lateral sclerosis: review of the neurobiological mechanisms and functional correlates;Brain Structure and Function;2023-11-24

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