Chronic Intermittent Sucrose Consumption Facilitates the Ability to Discriminate Opioid Receptor Blockade with Naltrexone in Rats
Jewett, David C, Liyanagamage, Donisha S N K, Avond, Mark A Vanden, Anderson, Molly A B, Twaroski, Kyleigh A, Marek, Morgan A, James, Kimberly F, Pal, Tapasya, Klockars, Anica, Olszewski, Pawel K, Levine, Allen S
Published in Nutrients (22.02.2022)
Published in Nutrients (22.02.2022)
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Severe Neonatal RYR1 Myopathy With Pathological Features of Congenital Muscular Dystrophy
Helbling, Daniel C, Mendoza, David, McCarrier, Julie, Vanden Avond, Mark A, Harmelink, Matthew M, Barkhaus, Paul E, Basel, Donald, Lawlor, Michael W
Published in Journal of neuropathology and experimental neurology (01.03.2019)
Published in Journal of neuropathology and experimental neurology (01.03.2019)
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Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
Hamm, Shelby E., Fathalikhani, Daniel D., Bukovec, Katherine E., Addington, Adele K., Zhang, Haiyan, Perry, Justin B., McMillan, Ryan P., Lawlor, Michael W., Prom, Mariah J., Vanden Avond, Mark A., Kumar, Suresh N., Coleman, Kirsten E., Dupont, J.B., Mack, David L., Brown, David A., Morris, Carl A., Gonzalez, J. Patrick, Grange, Robert W.
Published in Molecular therapy. Methods & clinical development (11.06.2021)
Published in Molecular therapy. Methods & clinical development (11.06.2021)
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Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
Hamm, Shelby E., Fathalikhani, Daniel D., Bukovec, Katherine E., Addington, Adele K., Zhang, Haiyan, Perry, Justin B., McMillan, Ryan P., Lawlor, Michael W., Prom, Mariah J., Vanden Avond, Mark A., Kumar, Suresh N., Coleman, Kirsten E., Dupont, J.B., Mack, David L., Brown, David A., Morris, Carl A., Gonzalez, J. Patrick, Grange, Robert W.
Published in Molecular therapy. Methods & clinical development (10.12.2021)
Published in Molecular therapy. Methods & clinical development (10.12.2021)
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The nucleotide prodrug CERC‐913 improves mtDNA content in primary hepatocytes from DGUOK‐deficient rats
Vanden Avond, Mark A., Meng, Hui, Beatka, Margaret J., Helbling, Daniel C., Prom, Mariah J., Sutton, Jessica L., Slick, Rebecca A., Dimmock, David P., Pertusati, Fabrizio, Serpi, Michaela, Pileggi, Elisa, Crutcher, Patrick, Thomas, Stephen, Lawlor, Michael W.
Published in Journal of inherited metabolic disease (01.03.2021)
Published in Journal of inherited metabolic disease (01.03.2021)
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High mobility group box 1 (HMGB1) is a potential disease biomarker in cell and mouse models of Duchenne muscular dystrophy
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
Published in Biology open (15.09.2024)
Published in Biology open (15.09.2024)
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Erratum: Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
Hamm, Shelby E, Fathalikhani, Daniel D, Bukovec, Katherine E, Addington, Adele K, Zhang, Haiyan, Perry, Justin B, McMillan, Ryan P, Lawlor, Michael W, Prom, Mariah J, Vanden Avond, Mark A, Kumar, Suresh N, Coleman, Kirsten E, Dupont, J B, Mack, David L, Brown, David A, Morris, Carl A, Gonzalez, J Patrick, Grange, Robert W
Published in Molecular therapy. Methods & clinical development (10.12.2021)
Published in Molecular therapy. Methods & clinical development (10.12.2021)
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Physiological role and mechanisms of action for a long noncoding haplotype region
Xue, Hong, Mishra, Manoj K, Liu, Yong, Liu, Pengyuan, Grzybowski, Michael, Pandey, Rajan, Usa, Kristie, Vanden Avond, Mark A, Bala, Niharika, Alli, Abdel A, Cowley, Allen W, Qiu, Qiongzi, Greene, Andrew S, Rao, Sridhar, O'Meara, Caitlin C, Geurts, Aron M, Liang, Mingyu
Published in bioRxiv (18.05.2024)
Published in bioRxiv (18.05.2024)
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