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	1.	The I4895T mutation in the type 1 ryanodine receptor induces fiber-type specific alterations in skeletal muscle that mimic premature aging. [electronic resource] by Boncompagni, Simona Loy, Ryan E Dirksen, Robert T Franzini-Armstrong, Clara Producer: 20110310 In: Aging cell vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Allele-specific gene silencing in two mouse models of autosomal dominant skeletal myopathy. [electronic resource] by Loy, Ryan E Lueck, John D Mostajo-Radji, Mohammed A Carrell, Ellie M Dirksen, Robert T Producer: 20130507 In: PloS one vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Crystal structure of dimeric cardiac L-type calcium channel regulatory domains bridged by Ca2+* calmodulins. [electronic resource] by Fallon, Jennifer L Baker, Mariah R Xiong, Liangwen Loy, Ryan E Yang, Guojun Dirksen, Robert T Hamilton, Susan L Quiocho, Florante A Producer: 20090507 In: Proceedings of the National Academy of Sciences of the United States of America vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum. [electronic resource] by Loy, Ryan E Orynbayev, Murat Xu, Le Andronache, Zoita Apostol, Simona Zvaritch, Elena MacLennan, David H Meissner, Gerhard Melzer, Werner Dirksen, Robert T Producer: 20110407 In: The Journal of general physiology vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line. [electronic resource] by Zvaritch, Elena Depreux, Frederic Kraeva, Natasha Loy, Ryan E Goonasekera, Sanjeewa A Boncompagni, Simona Boncompagi, Simona Kraev, Alexander Gramolini, Anthony O Dirksen, Robert T Franzini-Armstrong, Clara Seidman, Christine E Seidman, J G Maclennan, David H Producer: 20080102 In: Proceedings of the National Academy of Sciences of the United States of America vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene. [electronic resource] by Zhou, Haiyan Lillis, Suzanne Loy, Ryan E Ghassemi, Farshid Rose, Michael R Norwood, Fiona Mills, Kerry Al-Sarraj, Safa Lane, Russell J M Feng, Lucy Matthews, Emma Sewry, Caroline A Abbs, Stephen Buk, Stefan Hanna, Michael Treves, Susan Dirksen, Robert T Meissner, Gerhard Muntoni, Francesco Jungbluth, Heinz Producer: 20100608 In: Neuromuscular disorders : NMD vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)