Expression of mouse agrin in normal, denervated and dystrophic muscle
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Cited by 41 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. Deficiency of skeletal muscle Agrin contributes to the pathogenesis of age-related sarcopenia in mice;Cell Death & Disease;2024-03-09
2. Nerve pathology is prevented by linker proteins in mouse models forLAMA2-related muscular dystrophy;PNAS Nexus;2023-03-15
3. SMN controls neuromuscular junction integrity through U7 snRNP;Cell Reports;2022-09
4. Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons;Acta Neuropathologica;2022-08-10
5. Nerve pathology is prevented by linker proteins in mouse models for LAMA2-related muscular dystrophy;2022-05-20
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