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Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy.
Willmann R, Gordish-Dressman H, Meinen S, Rüegg MA, Yu Q, Nagaraju K, Kumar A, Girgenrath M, Coffey CBM, Cruz V, Van Ry PM, Bogdanik L, Lutz C, Rutkowski A, Burkin DJ. Willmann R, et al. Among authors: van ry pm. J Neuromuscul Dis. 2017;4(2):115-126. doi: 10.3233/JND-170217. J Neuromuscul Dis. 2017. PMID: 28550268 Free PMC article. Review.
PTRH2 gene mutation causes progressive congenital skeletal muscle pathology.
Doe J, Kaindl AM, Jijiwa M, de la Vega M, Hu H, Griffiths GS, Fontelonga TM, Barraza P, Cruz V, Van Ry P, Ramos JW, Burkin DJ, Matter ML. Doe J, et al. Hum Mol Genet. 2017 Apr 15;26(8):1458-1464. doi: 10.1093/hmg/ddx048. Hum Mol Genet. 2017. PMID: 28175314 Free PMC article.
Bit-1 is an essential regulator of myogenic differentiation.
Griffiths GS, Doe J, Jijiwa M, Van Ry P, Cruz V, de la Vega M, Ramos JW, Burkin DJ, Matter ML. Griffiths GS, et al. J Cell Sci. 2015 May 1;128(9):1707-17. doi: 10.1242/jcs.158964. Epub 2015 Mar 13. J Cell Sci. 2015. PMID: 25770104 Free PMC article.
Treatment with galectin-1 improves myogenic potential and membrane repair in dysferlin-deficient models.
Vallecillo-Zúniga ML, Rathgeber MF, Poulson PD, Hayes S, Luddington JS, Gill HN, Teynor M, Kartchner BC, Valdoz J, Stowell C, Markham AR, Arthur C, Stowell S, Van Ry PM. Vallecillo-Zúniga ML, et al. Among authors: van ry pm. PLoS One. 2020 Sep 3;15(9):e0238441. doi: 10.1371/journal.pone.0238441. eCollection 2020. PLoS One. 2020. PMID: 32881965 Free PMC article.
Evaluating Therapeutic Activity of Galectin-1 in Sarcolemma Repair of Skeletal Muscle.
Vallecillo-Zúniga ML, Rathgeber M, Poulson D, Kartchner B, Luddington J, Gill H, Hayes S, Teynor M, Stowell CS, Arthur CM, Stowell SR, Van Ry PM. Vallecillo-Zúniga ML, et al. Among authors: van ry pm. Methods Mol Biol. 2022;2442:663-683. doi: 10.1007/978-1-0716-2055-7_36. Methods Mol Biol. 2022. PMID: 35320552
24 results