Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Hailie N Gill"'
Autor:
Mary L Vallecillo-Zúniga, Matthew F Rathgeber, P Daniel Poulson, Spencer Hayes, Jacob S Luddington, Hailie N Gill, Matthew Teynor, Braden C Kartchner, Jonard Valdoz, Caleb Stowell, Ashley R Markham, Connie Arthur, Sean Stowell, Pam M Van Ry
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0238441 (2020)
Limb-girdle muscular dystrophy type 2B (LGMD2B) is caused by mutations in the dysferlin gene, resulting in non-functional dysferlin, a key protein found in muscle membrane. Treatment options available for patients are chiefly palliative in nature and
Externí odkaz:
https://doaj.org/article/1b0d5091b3e842558ddcb01bd5b3fcc0
Autor:
Hailie N. Gill, Mary L. Vallecillo-Zúniga, Matthew F. Rathgeber, Christian J Arnold, Spencer Hayes, Pam M. Van Ry, Braden C. Kartchner, Peter Daniel Poulson, Ethan L. Dodson, Jacob S. Luddington, Seth R. Garfield, Sean R. Stowell, Connie M Arthur, Jonathan L Spallino, Jonard Corpuz Valdoz
Publikováno v:
Cells
Volume 10
Issue 11
Cells, Vol 10, Iss 3210, p 3210 (2021)
Volume 10
Issue 11
Cells, Vol 10, Iss 3210, p 3210 (2021)
Two of the main pathologies characterizing dysferlinopathies are disrupted muscle membrane repair and chronic inflammation, which lead to symptoms of muscle weakness and wasting. Here, we used recombinant human Galectin-1 (rHsGal-1) as a therapeutic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d4d3f7638b2a6da765b7aea93af0f5