Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of laminin-α2 related congenital muscular dystrophy.
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| Title: | Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of laminin-α2 related congenital muscular dystrophy. |
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| Authors: | Barraza-Flores P; Department of Pharmacology, Reno School of Medicine, University of Nevada, Reno, NV 89557, USA., Bukovec KE; Department of Human Nutrition, Foods, and Exercise, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA., Dagda M; Department of Pharmacology, Reno School of Medicine, University of Nevada, Reno, NV 89557, USA., Conner BW; Department of Pharmacology, Reno School of Medicine, University of Nevada, Reno, NV 89557, USA., Oliveira-Santos A; Department of Pharmacology, Reno School of Medicine, University of Nevada, Reno, NV 89557, USA., Grange RW; Department of Human Nutrition, Foods, and Exercise, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA., Burkin DJ; Department of Pharmacology, Reno School of Medicine, University of Nevada, Reno, NV 89557, USA. |
| Source: | Human molecular genetics [Hum Mol Genet] 2020 Aug 03; Vol. 29 (13), pp. 2162-2170. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1460-2083 |
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| DOI: | 10.1093/hmg/ddaa104 |
