Ryan E. Loy
0009-0004-7325-1772
Publication & Citation Trends
Publications
0 total
High-Throughput Covalent Modifier Screening with Acoustic Ejection Mass Spectrometry.
Cited by 13
Semantic Scholar
Allele-Specific Gene Silencing in Two Mouse Models of Autosomal Dominant Skeletal Myopathy OA
Cited by 20
Semantic Scholar
Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum OA
Cited by 81
Semantic Scholar
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene. OA
Cited by 89
Semantic Scholar
Allele Specific Gene Silencing in Autosomal-Dominant Skeletal Myopathies OA
Cited by 0
Semantic Scholar
The I4895T mutation in the type 1 ryanodine receptor induces fiber‐type specific alterations in skeletal muscle that mimic premature aging OA
Cited by 44
Semantic Scholar
Altered Type 1 Ryanodine Receptor Activity and Functional Rescue In a Mouse Model of Central Core Disease
Cited by 0
Semantic Scholar
ryanodine receptor Ca 2+ ion permeation and release from the sarcoplasmic reticulum
Cited by 0
Semantic Scholar
Research Topics
Ion channel regulation and function
(10)
Cardiac electrophysiology and arrhythmias
(4)
Cardiomyopathy and Myosin Studies
(3)
Genetic Neurodegenerative Diseases
(2)
Viral Infections and Immunology Research
(2)
Affiliations
University of Rochester Medical Center
University of Rochester