Increased IGF-1 in muscle modulates the phenotype of severe SMA mice-Reference-Cited by-同舟云学术

Increased IGF-1 in muscle modulates the phenotype of severe SMA mice

Published:2011-02-16 Issue:9 Volume:20 Page:1844-1853
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Bosch-Marcé Marta,Wee Claribel D.,Martinez Tara L.,Lipkes Celeste E.,Choe Dong W.,Kong Lingling,Van Meerbeke James P.,Musarò Antonio,Sumner Charlotte J.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/20/9/1844/17255511/ddr067.pdf

Reference56 articles.

1. The neurobiology of childhood spinal muscular atrophy;Crawford;Neurobiol. Dis.,1996

2. Identification and characterization of a spinal muscular atrophy-determining gene;Lefebvre;Cell,1995

3. Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism;Fidzianska;Brain,1990

4. Childhood spinal muscular atrophy induces alterations in contractile and regulatory protein isoform expressions;Stevens;Neuropathol. Appl. Neurobiol.,2008

Cited by 93 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. Depletion of SMN protein in mesenchymal progenitors impairs the development of bone and neuromuscular junction in spinal muscular atrophy;eLife;2024-02-06

2. Depletion of SMN Protein in Mesenchymal Progenitors Impairs the Development of Bone and Neuromuscular Junction in Spinal Muscular Atrophy;ELIFE;2024-01-23

3. Depletion of SMN Protein in Mesenchymal Progenitors Impairs the Development of Bone and Neuromuscular Junction in Spinal Muscular Atrophy;2024-01-23

4. Depletion of SMN Protein in Mesenchymal Progenitors Impairs the Development of Bone and Neuromuscular Junction in Spinal Muscular Atrophy;2023-10-10

5. Time-Dependent Changes in Muscle IGF1-IGFBP5-PAPP System after Sciatic Denervation;International Journal of Molecular Sciences;2023-09-14