CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies von Alexander, Matthew S., Rozkalne, Anete, Colletta, Alessandro, Spinazzola, Janelle M., Johnson, Samuel, Rahimov, Fedik, Meng, Hui, Lawlor, Michael W., Estrella, Elicia, Kunkel, Louis M., Gussoni, Emanuela

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Loss of Mtm1 causes cholestatic liver disease in a model of X-linked myotubular myopathy von Karolczak, Sophie, Deshwar, Ashish R, Aristegui, Evangelina, Kamath, Binita M, Lawlor, Michael W, Andreoletti, Gaia, Volpatti, Jonathan R, Ellis, Jillian L, Yin, Chunyue, Dowling, James J

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Muscle‐directed gene therapy corrects Pompe disease and uncovers species‐specific GAA immunogenicity von Eggers, Michelle, Vannoy, Charles H, Huang, Jianyong, Purushothaman, Pravinkumar, Brassard, Jacqueline, Fonck, Carlos, Meng, Hui, Prom, Mariah J, Lawlor, Michael W, Cunningham, Justine, Sadhu, Chanchal, Mavilio, Fulvio

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Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy von Ceyhan-Birsoy, Ozge, Agrawal, Pankaj B., Hidalgo, Carlos, Schmitz-Abe, Klaus, DeChene, Elizabeth T., Swanson, Lindsay C., Soemedi, Rachel, Vasli, Nasim, Iannaccone, Susan T., Shieh, Perry B., Shur, Natasha, Dennison, Jane M., Lawlor, Michael W., Laporte, Jocelyn, Markianos, Kyriacos, Fairbrother, William G., Granzier, Henk, Beggs, Alan H.

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TNNT1 nemaline myopathy: natural history and therapeutic frontier von Fox, Michael D, Carson, Vincent J, Feng, Han-Zhong, Lawlor, Michael W, Gray, John T, Brigatti, Karlla W, Jin, J -P, Strauss, Kevin A

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Duchenne muscular dystrophy (DMD) cardiomyocyte-secreted exosomes promote the pathogenesis of DMD-associated cardiomyopathy von Gartz, Melanie, Lin, Chien-Wei, Sussman, Mark A., Lawlor, Michael W., Strande, Jennifer L.

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Prolonged duration local anesthesia with minimal toxicity von Epstein-Barash, Hila, Shichor, Iris, Kwon, Albert H, Hall, Sherwood, Lawlor, Michael W, Langer, Robert, Kohane, Daniel S

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Mechanosensory and ATP Release Deficits following Keratin14-Cre-Mediated TRPA1 Deletion Despite Absence of TRPA1 in Murine Keratinocytes von Zappia, Katherine J, Garrison, Sheldon R, Palygin, Oleg, Weyer, Andy D, Barabas, Marie E, Lawlor, Michael W, Staruschenko, Alexander, Stucky, Cheryl L

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Putting It All Together: Postmortem Diagnosis of a Rare Ichthyosis Syndrome von Jain, Pragya Virendrakumar, Maxey, Jauntea, W Lawlor, Michael, Parsons, Lauren N

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Dystrophin-deficient cardiomyocytes derived from human urine: New biologic reagents for drug discovery von Guan, Xuan, Mack, David L., Moreno, Claudia M., Strande, Jennifer L., Mathieu, Julie, Shi, Yingai, Markert, Chad D., Wang, Zejing, Liu, Guihua, Lawlor, Michael W., Moorefield, Emily C., Jones, Tara N., Fugate, James A., Furth, Mark E., Murry, Charles E., Ruohola-Baker, Hannele, Zhang, Yuanyuan, Santana, Luis F., Childers, Martin K.

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Cardioprotective effect of nicorandil on isoproterenol induced cardiomyopathy in the Mdx mouse model von Sullivan, Rachel T., Lam, Ngoc T., Haberman, Margaret, Beatka, Margaret J., Afzal, Muhammad Z., Lawlor, Michael W., Strande, Jennifer L.

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Clonally Focused Public and Private T Cells in Resected Brain Tissue From Surgeries to Treat Children With Intractable Seizures von Chang, Julia W., Reyes, Samuel D., Faure-Kumar, Emmanuelle, Lam, Sandi K., Lawlor, Michael W., Leventer, Richard J., Lew, Sean M., Lockhart, Paul J., Pope, Kathryn, Weiner, Howard L., Salamon, Noriko, Vinters, Harry V., Mathern, Gary W., Fallah, Aria, Owens, Geoffrey C.

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X-linked myotubular myopathy von Lawlor, Michael W., Dowling, James J.

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Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function von Hall, Arielle, Fontelonga, Tatiana, Wright, Alec, Gwilt, Katlynn Bugda, Widrick, Jeffrey, Pasut, Alessandra, Villa, Francesco, Miranti, Cynthia K., Gibbs, Devin, Jiang, Evan, Meng, Hui, Lawlor, Michael W., Gussoni, Emanuela

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rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy von Ross, Jacob A., Tasfaout, Hichem, Levy, Yotam, Morgan, Jennifer, Cowling, Belinda S., Laporte, Jocelyn, Zanoteli, Edmar, Romero, Norma B., Lowe, Dawn A., Jungbluth, Heinz, Lawlor, Michael W., Mack, David L., Ochala, Julien

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AAV8 gene therapy reverses cardiac pathology and prevents early mortality in a mouse model of Friedreich’s ataxia von Chang, Joshua C., Ryan, Molly R., Stark, Marie C., Liu, Su, Purushothaman, Pravinkumar, Bolan, Fria, Johnson, Caitlin A., Champe, Mark, Meng, Hui, Lawlor, Michael W., Halawani, Sarah, Ngaba, Lucie V., Lynch, David R., Davis, Crystal, Gonzalo-Gil, Elena, Lutz, Cathleen, Urbinati, Fabrizia, Medicherla, Bala, Fonck, Carlos

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High mobility group box 1 (HMGB1) is a potential disease biomarker in cell and mouse models of Duchenne muscular dystrophy von Slick, Rebecca A, Sutton, Jessica, Haberman, Margaret, O'Brien, Benjamin S, Tinklenberg, Jennifer A, Mardikar, Aashay, Prom, Mariah J, Beatka, Margaret, Gartz, Melanie, Vanden Avond, Mark A, Siebers, Emily, Mack, David L, Gonzalez, J Patrick, Ebert, Allison D, Nagaraju, Kanneboyina, Lawlor, Michael W

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Whole-thorax irradiation induces hypoxic respiratory failure, pleural effusions and cardiac remodeling von Medhora, Meetha, Gao, Feng, Glisch, Chad, Narayanan, Jayashree, Sharma, Ashish, Harmann, Leanne M., Lawlor, Michael W., Snyder, Laura A., Fish, Brian L., Down, Julian D., Moulder, John E., Strande, Jennifer L., Jacobs, Elizabeth R.

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Effects of Regulatory T Cell Depletion in BALB/c Mice Infected with Low Doses of Borrelia burgdorferi von Santiago, Kaitlyn N, Kozlik, Tanya, Liedhegner, Elizabeth S, Slick, Rebecca A, Lawlor, Michael W, Nardelli, Dean T

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Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency von Nagree, Murtaza S., Rybova, Jitka, Kleynerman, Annie, Ahrenhoerster, Carissa J., Saville, Jennifer T., Xu, TianMeng, Bachochin, Maxwell, McKillop, William M., Lawlor, Michael W., Pshezhetsky, Alexey V., Isaeva, Olena, Budde, Matthew D., Fuller, Maria, Medin, Jeffrey A.

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