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      Exploratory Profiling of Urine MicroRNAs in the dy 2J/dy 2J Mouse Model of LAMA2-CMD: Relation to Disease Progression

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          Abstract

          Circulating microRNAs (miRNAs) are being considered as non-invasive biomarkers for disease progression and clinical trials. Congenital muscular dystrophy with deficiency of laminin α2 chain (LAMA2-CMD) is a very severe form of muscular dystrophy, for which no treatment is available. In order to identify LAMA2-CMD biomarkers we have profiled miRNAs in urine from the dy 2J / dy 2J mouse model of LAMA2-CMD at three distinct time points (representing asymptomatic, initial and established disease). We demonstrate that unique groups of miRNAs are differentially expressed at each time point. We suggest that urine miRNAs can be sensitive biomarkers for different stages of LAMA2-CMD.

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          Author and article information

          Contributors
          Journal
          PLoS Curr
          PLoS Curr
          plos
          PLoS Currents
          Public Library of Science (San Francisco, USA )
          2157-3999
          27 August 2018
          : 10
          : ecurrents.md.d0c203c018bc024f2f4c9791ecb05f88
          Affiliations
          PhD Student, Experimental Medical Science, Lund University, Lund, Sweden
          Muscle Biology Unit, Lund University, Lund, Sweden
          Integrative Biology and Physiology, University of California, Los Angeles, California, United States
          Article
          10.1371/currents.md.d0c203c018bc024f2f4c9791ecb05f88
          6140833
          b66a5f1a-e557-4dca-ba3b-28781bf3760f
          © 2018 Moreira Soares Oliveira, Gawlik, Durbeej, Holmberg, et al

          This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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          Funding
          This work was supported by the following funding agencies: CNPq, Association Française contre les Myopathies, Crafoord foundation, Greta and Johan Kock foundation, Lars Hierta foundation, Olle Engkvist Byggmästare foundation, Royal Physiographic Society in Lund, Swedish Research Council, Thelma Zoéga foundation, Österlund foundation, Anna and Edwin Berger foundation. The funding agencies had no influence on study design, data acquisition or manuscript preparation. The authors have declared that no competing interests exist.
          Categories
          Animal Models

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