The inflammatory pathology of dysferlinopathy is distinct from calpainopathy, Becker muscular dystrophy, and inflammatory myopathies by Nicole Becker, Steven A. Moore, Karra A. Jones

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Elevated oxidative membrane damage associated with genetic modifiers of Lyst-mutant phenotypes. by Colleen M Trantow, Adam Hedberg-Buenz, Sachiyo Iwashita, Steven A Moore, Michael G Anderson

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Ventriculus terminalis cyst in an infant: a case report by Arnold H. Menezes, Yutaka Sato, Brian J. Dlouhy, Karra A. Jones, Steven A. Moore

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Differential activation of catalase expression and activity by PPAR agonists: Implications for astrocyte protection in anti-glioma therapy by Nicholas K.H. Khoo, Sachin Hebbar, Weiling Zhao, Steven A. Moore, Frederick E. Domann, Mike E. Robbins

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Thirty-Year Follow-Up of Early Onset Amyotrophic Lateral Sclerosis with a Pathogenic Variant in SPTLC1 by Aparna Ajjarapu, Shawna ME. Feely, Michael E. Shy, Christina Trout, Stephan Zuchner, Steven A. Moore, Katherine D. Mathews

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Docosahexaenoic acid synthesis from n-3 polyunsaturated fatty acids in differentiated rat brain astrocytes by Deborah E. Williard, Shawn D. Harmon, Terry L. Kaduce, Meredith Preuss, Steven A. Moore, Michael E.C. Robbins, Arthur A. Spector

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Myopathic lamin mutations cause reductive stress and activate the nrf2/keap-1 pathway. by George Dialynas, Om K Shrestha, Jessica M Ponce, Monika Zwerger, Dylan A Thiemann, Grant H Young, Steven A Moore, Liping Yu, Jan Lammerding, Lori L Wallrath

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Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation by Nivedita U. Jerath, Cameron D. Crockett, Steven A. Moore, Michael E. Shy, Conrad C. Weihl, Tsui-Fen Chou, Tiffany Grider, Michael A. Gonzalez, Stephan Zuchner, Andrea Swenson

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A De Novo Sequence Variant in Barrier-to-Autointegration Factor Is Associated with Dominant Motor Neuronopathy by Agathe Marcelot, Felipe Rodriguez-Tirado, Philippe Cuniasse, Mei-ling Joiner, Simona Miron, Alexey A. Soshnev, Mimi Fang, Miles A. Pufall, Katherine D. Mathews, Steven A. Moore, Sophie Zinn-Justin, Pamela K. Geyer

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TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy by Austin A. Larson, Peter R. Baker, Miroslav P. Milev, Craig A. Press, Ronald J. Sokol, Mary O. Cox, Jacqueline K. Lekostaj, Aaron A. Stence, Aaron D. Bossler, Jennifer M. Mueller, Keshika Prematilake, Thierry Fotsing Tadjo, Charles A. Williams, Michael Sacher, Steven A. Moore

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The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition by Jeremy L Praissman, Tobias Willer, M Osman Sheikh, Ants Toi, David Chitayat, Yung-Yao Lin, Hane Lee, Stephanie H Stalnaker, Shuo Wang, Pradeep Kumar Prabhakar, Stanley F Nelson, Derek L Stemple, Steven A Moore, Kelley W Moremen, Kevin P Campbell, Lance Wells

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