Genetic modifiers of Duchenne and facioscapulohumeral muscular dystrophies von Hightower, Rylie M., Alexander, Matthew S.

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hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies von Alexander, Matthew S., Hightower, Rylie M., Reid, Andrea L., Bennett, Alexis H., Iyer, Lakshmanan, Slonim, Donna K., Saha, Madhurima, Kawahara, Genri, Kunkel, Louis M., Kopin, Alan S., Gupta, Vandana A., Kang, Peter B., Draper, Isabelle

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Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy von Saha, Madhurima, Rizzo, Skylar A, Ramanathan, Manashwi, Hightower, Rylie M, Santostefano, Katherine E, Terada, Naohiro, Finkel, Richard S, Berg, Jonathan S, Chahin, Nizar, Pacak, Christina A, Wagner, Richard E, Alexander, Matthew S, Draper, Isabelle, Kang, Peter B

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The SINE Compound KPT-350 Blocks Dystrophic Pathologies in DMD Zebrafish and Mice von Hightower, Rylie M., Reid, Andrea L., Gibbs, Devin E., Wang, Yimin, Widrick, Jeffrey J., Kunkel, Louis M., Kastenschmidt, Jenna M., Villalta, S. Armando, van Groen, Thomas, Chang, Hua, Gornisiewicz, Savanna, Landesman, Yosef, Tamir, Sharon, Alexander, Matthew S.

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DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies von Reid, Andrea L, Wang, Yimin, Samani, Adrienne, Hightower, Rylie M, Lopez, Michael A, Gilbert, Shawn R, Ianov, Lara, Crossman, David K, Dell’Italia, Louis J, Millay, Douglas P, van Groen, Thomas, Halade, Ganesh V, Alexander, Matthew S

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miR-486 is essential for muscle function and suppresses a dystrophic transcriptome von Samani, Adrienne, Hightower, Rylie M, Reid, Andrea L, English, Katherine G, Lopez, Michael A, Doyle, J Scott, Conklin, Michael J, Schneider, David A, Bamman, Marcas M, Widrick, Jeffrey J, Crossman, David K, Xie, Min, Jee, David, Lai, Eric C, Alexander, Matthew S

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A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies von Serafini, Peter R, Feyder, Michael J, Hightower, Rylie M, Garcia-Perez, Daniela, Vieira, Natássia M, Lek, Angela, Gibbs, Devin E, Moukha-Chafiq, Omar, Augelli-Szafran, Corinne E, Kawahara, Genri, Widrick, Jeffrey J, Kunkel, Louis M, Alexander, Matthew S

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Genetic modifiers of D uchenne and facioscapulohumeral muscular dystrophies von Hightower, Rylie M., Alexander, Matthew S.

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A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies von Serafini, Peter R., Feyder, Michael J., Hightower, Rylie M., Garcia-Perez, Daniela, Vieira, Natássia M., Lek, Angela, Gibbs, Devin E., Moukha-Chafiq, Omar, Augelli-Szafran, Corinne E., Kawahara, Genri, Widrick, Jeffrey J., Kunkel, Louis M., Alexander, Matthew S.

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Therapeutic Effect of KPT-350 in a Preclinical Model of Duchenne Muscular Dystrophy (S42.003) von Gibbs, Devin, Hightower, Rylie, Lee, Christopher, Spinazzola, Janelle, Mead, Lillian, Widrick, Jeffrey, Tamir, Sharon, Cochran, Shelton, Landesman, Yosef, Kunkel, Louis, Alexander, Matthew

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