Search Results - Sher, Roger B.
- Showing 1 - 12 results of 12
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mdm Muscular Dystrophy: Interactions with Calpain 3 and a Novel Functional Role for Titin’s N2A Domain by Huebsch, Kimberly A., Kudryashova, Elena, Wooley, Christine M., Sher, Roger B., Seburn, Kevin L., Spencer, Melissa J., Cox, Gregory A.
Published 2005Text -
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Choline kinase beta is required for normal endochondral bone formation by Li, Zhuo, Wu, Gengshu, Sher, Roger B., Khavandgar, Zohreh, Hermansson, Martin, Cox, Gregory A., Doschak, Michael R., Murshed, Monzur, Beier, Frank, Vance, Dennis E.
Published 2014Text -
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Genetic Background Effects on Disease Onset and Lifespan of the Mutant Dynactin p150(Glued) Mouse Model of Motor Neuron Disease by Heiman-Patterson, Terry D., Blankenhorn, Elizabeth P., Sher, Roger B., Jiang, Juliann, Welsh, Priscilla, Dixon, Meredith C., Jeffrey, Jeremy I., Wong, Philip, Cox, Gregory A., Alexander, Guillermo M.
Published 2015Text -
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Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy by Mitsuhashi, Satomi, Hatakeyama, Hideyuki, Karahashi, Minako, Koumura, Tomoko, Nonaka, Ikuya, Hayashi, Yukiko K., Noguchi, Satoru, Sher, Roger B., Nakagawa, Yasuhito, Manfredi, Giovanni, Goto, Yu-ichi, Cox, Gregory A., Nishino, Ichizo
Published 2011Text -
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A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis by Mitsuhashi, Satomi, Ohkuma, Aya, Talim, Beril, Karahashi, Minako, Koumura, Tomoko, Aoyama, Chieko, Kurihara, Mana, Quinlivan, Ros, Sewry, Caroline, Mitsuhashi, Hiroaki, Goto, Kanako, Koksal, Burcu, Kale, Gulsev, Ikeda, Kazutaka, Taguchi, Ryo, Noguchi, Satoru, Hayashi, Yukiko K., Nonaka, Ikuya, Sher, Roger B., Sugimoto, Hiroyuki, Nakagawa, Yasuhito, Cox, Gregory A., Topaloglu, Haluk, Nishino, Ichizo
Published 2011Text -
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NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease by Martin, Paige B., Kigoshi-Tansho, Yu, Sher, Roger B., Ravenscroft, Gianina, Stauffer, Jennifer E., Kumar, Rajesh, Yonashiro, Ryo, Müller, Tina, Griffith, Christopher, Allen, William, Pehlivan, Davut, Haral, Tamar, Zenker, Martin, Howting, Denise, Schanze, Denny, Faqeih, Eissa A., Almontashiri, Naif A. M., Maroofian, Reza, Houlden, Henry, Mazaheri, Neda, Galehdari, Hamid, Douglas, Ganka, Posey, Jennifer E., Ryan, Monique, Lupski, James R., Laing, Nigel G., Joazeiro, Claudio A. P., Cox, Gregory A.
Published 2020Text -
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Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease by Martin, Paige B., Kigoshi-Tansho, Yu, Sher, Roger B., Ravenscroft, Gianina, Stauffer, Jennifer E., Kumar, Rajesh, Yonashiro, Ryo, Müller, Tina, Griffith, Christopher, Allen, William, Pehlivan, Davut, Harel, Tamar, Zenker, Martin, Howting, Denise, Schanze, Denny, Faqeih, Eissa A., Almontashiri, Naif A. M., Maroofian, Reza, Houlden, Henry, Mazaheri, Neda, Galehdari, Hamid, Douglas, Ganka, Posey, Jennifer E., Ryan, Monique, Lupski, James R., Laing, Nigel G., Joazeiro, Claudio A. P., Cox, Gregory A.
Published 2020Text