| Year |
Citation |
Score |
| 2012 |
Loy RE, Lueck JD, Mostajo-Radji MA, Carrell EM, Dirksen RT. Allele-specific gene silencing in two mouse models of autosomal dominant skeletal myopathy. Plos One. 7: e49757. PMID 23152933 DOI: 10.1371/Journal.Pone.0049757 |
0.671 |
|
| 2011 |
Loy RE, Orynbayev M, Xu L, Andronache Z, Apostol S, Zvaritch E, MacLennan DH, Meissner G, Melzer W, Dirksen RT. Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum. The Journal of General Physiology. 137: 43-57. PMID 21149547 DOI: 10.1085/Jgp.201010523 |
0.749 |
|
| 2010 |
Boncompagni S, Loy RE, Dirksen RT, Franzini-Armstrong C. The I4895T mutation in the type 1 ryanodine receptor induces fiber-type specific alterations in skeletal muscle that mimic premature aging. Aging Cell. 9: 958-70. PMID 20961389 DOI: 10.1111/J.1474-9726.2010.00623.X |
0.698 |
|
| 2010 |
Zhou H, Lillis S, Loy RE, Ghassemi F, Rose MR, Norwood F, Mills K, Al-Sarraj S, Lane RJ, Feng L, Matthews E, Sewry CA, Abbs S, Buk S, Hanna M, et al. Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders : Nmd. 20: 166-73. PMID 20080402 DOI: 10.1016/J.Nmd.2009.12.005 |
0.627 |
|
| 2010 |
Loy RE, Mostajo-Radji MA, Lueck JD, Dirksen RT. Allele Specific Gene Silencing in Autosomal-Dominant Skeletal Myopathies Biophysical Journal. 98: 712a-713a. DOI: 10.1016/J.Bpj.2009.12.3908 |
0.693 |
|
| 2009 |
Fallon JL, Baker MR, Xiong L, Loy RE, Yang G, Dirksen RT, Hamilton SL, Quiocho FA. Crystal structure of dimeric cardiac L-type calcium channel regulatory domains bridged by Ca2+* calmodulins. Proceedings of the National Academy of Sciences of the United States of America. 106: 5135-40. PMID 19279214 DOI: 10.1073/Pnas.0807487106 |
0.624 |
|
| 2009 |
Loy RE, Apostol S, Orynbayev M, Andronache Z, Zvaritch E, MacLennan DH, Melzer W, Dirksen RT. Deficits in Ca2+ Release and in vivo Muscle Strength in Heterozygous I4895T RyR1 Knock-In Mice Biophysical Journal. 96: 236a. DOI: 10.1016/J.Bpj.2008.12.1160 |
0.708 |
|
| 2007 |
Zvaritch E, Depreux F, Kraeva N, Loy RE, Goonasekera SA, Boncompagni S, Boncompagi S, Kraev A, Gramolini AO, Dirksen RT, Franzini-Armstrong C, Seidman CE, Seidman JG, Maclennan DH. An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line. Proceedings of the National Academy of Sciences of the United States of America. 104: 18537-42. PMID 18003898 DOI: 10.1073/Pnas.0709312104 |
0.733 |
|
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