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Christopher M. Chamberlain, Ph.D. - Publications

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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10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Razzoli M, Lindsay A, Law ML, Chamberlain CM, Southern WM, Berg M, Osborn J, Engeland WC, Metzger JM, Ervasti JM, Bartolomucci A. Social stress is lethal in the mdx model of Duchenne muscular dystrophy. Ebiomedicine. 102700. PMID 32192914 DOI: 10.1016/J.Ebiom.2020.102700  0.369
2018 Lindsay A, Chamberlain CM, Witthuhn BA, Lowe DA, Ervasti JM. Dystrophinopathy associated dysfunction of Krebs cycle metabolism. Human Molecular Genetics. PMID 30476171 DOI: 10.1093/Hmg/Ddy404  0.547
2018 Patrinostro X, Roy P, Lindsay A, Chamberlain CM, Sundby LJ, Starker CG, Voytas DF, Ervasti JM, Perrin BJ. Essential nucleotide- and protein-dependent functions of /β-actin. Proceedings of the National Academy of Sciences of the United States of America. PMID 30012594 DOI: 10.1073/Pnas.1807895115  0.404
2018 Lindsay A, Schmiechen A, Chamberlain CM, Ervasti JM, Lowe DA. Neopterin/7,8-dihydroneopterin is elevated in Duchenne muscular dystrophy patients and protects mdx skeletal muscle function. Experimental Physiology. PMID 29791760 DOI: 10.1113/Ep087031  0.529
2017 McCourt JL, Talsness DM, Lindsay A, Arpke RW, Chatterton PD, Nelson DM, Chamberlain CM, Olthoff JT, Belanto JJ, McCourt PM, Kyba M, Lowe DA, Ervasti JM. Mouse models of two missense mutations in actin binding domain 1 of dystrophin associated with Duchenne or Becker muscular dystrophy. Human Molecular Genetics. PMID 29194514 DOI: 10.1093/Hmg/Ddx414  0.475
2017 Patrinostro X, O'Rourke AR, Chamberlain CM, Moriarity BS, Perrin BJ, Ervasti JM. Relative importance of βcyto- and γcyto-actin in primary mouse embryonic fibroblasts. Molecular Biology of the Cell. PMID 28077619 DOI: 10.1091/Mbc.E16-07-0503  0.414
2016 Belanto JJ, Olthoff JT, Mader TL, Chamberlain CM, Nelson DM, McCourt PM, Talsness DM, Gundersen GG, Lowe DA, Ervasti JM. Independent variability of microtubule perturbations associated with dystrophinopathy. Human Molecular Genetics. 25: 4951-4961. PMID 28171583 DOI: 10.1093/Hmg/Ddw318  0.516
2016 Belanto JJ, Olthoff JT, Mader TL, Chamberlain CM, Nelson DM, McCourt PM, Talsness DM, Gunderson GG, Lowe DA, Ervasti JM. Independent variability of microtubule perturbations associated with dystrophinopathy. Human Molecular Genetics. PMID 27638889 DOI: 10.1093/hmg/ddw318  0.478
2013 Lee KY, Li M, Manchanda M, Batra R, Charizanis K, Mohan A, Warren SA, Chamberlain CM, Finn D, Hong H, Ashraf H, Kasahara H, Ranum LP, Swanson MS. Compound loss of muscleblind-like function in myotonic dystrophy. Embo Molecular Medicine. 5: 1887-900. PMID 24293317 DOI: 10.1002/Emmm.201303275  0.541
2012 Chamberlain CM, Ranum LP. Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise. Human Molecular Genetics. 21: 4645-54. PMID 22846424 DOI: 10.1093/Hmg/Dds306  0.556
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