Christopher M. Chamberlain, Ph.D.

Affiliations: 
2012 Molecular, Cellular, Developmental Biology and Genetics University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Genetics, Molecular Biology, General Biology
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"Christopher Chamberlain"
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Parents

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Laura P. Ranum grad student 2012 UMN
 (Mouse model of Muscleblind-like 1 overexpression: Therapeutic promise and multisystemic effects.)
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Publications

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Razzoli M, Lindsay A, Law ML, et al. (2020) Social stress is lethal in the mdx model of Duchenne muscular dystrophy. Ebiomedicine. 102700
Lindsay A, Chamberlain CM, Witthuhn BA, et al. (2018) Dystrophinopathy associated dysfunction of Krebs cycle metabolism. Human Molecular Genetics
Patrinostro X, Roy P, Lindsay A, et al. (2018) Essential nucleotide- and protein-dependent functions of /β-actin. Proceedings of the National Academy of Sciences of the United States of America
Lindsay A, Schmiechen A, Chamberlain CM, et al. (2018) Neopterin/7,8-dihydroneopterin is elevated in Duchenne muscular dystrophy patients and protects mdx skeletal muscle function. Experimental Physiology
McCourt JL, Talsness DM, Lindsay A, et al. (2017) Mouse models of two missense mutations in actin binding domain 1 of dystrophin associated with Duchenne or Becker muscular dystrophy. Human Molecular Genetics
Patrinostro X, O'Rourke AR, Chamberlain CM, et al. (2017) Relative importance of βcyto- and γcyto-actin in primary mouse embryonic fibroblasts. Molecular Biology of the Cell
Belanto JJ, Olthoff JT, Mader TL, et al. (2016) Independent variability of microtubule perturbations associated with dystrophinopathy. Human Molecular Genetics. 25: 4951-4961
Belanto JJ, Olthoff JT, Mader TL, et al. (2016) Independent variability of microtubule perturbations associated with dystrophinopathy. Human Molecular Genetics
Lee KY, Li M, Manchanda M, et al. (2013) Compound loss of muscleblind-like function in myotonic dystrophy. Embo Molecular Medicine. 5: 1887-900
Chamberlain CM, Ranum LP. (2012) Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise. Human Molecular Genetics. 21: 4645-54
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