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 BiologyGoogle:
"Christopher Chamberlain"Mean distance: 42746.4
Parents
Sign in to add mentorLaura 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 |