Results 121 to 130 of about 11,986 (188)

Old dog, new trick: Charybdotoxin as a novel ryanodine receptor blocker. [PDF]

J Physiol
Magyar ZÉ, Hevesi J, Mészáros F, Bozsó Z, Szolomájer J, Tóth G, Panyi G, Enyedi P, Varga Z, Pethő Z, Almássy J.   +10 more
europepmc   +1 more source

Whole-Genome Sequencing Reveals Population Structure, Genetic Diversity, and Selection Signatures in Kazakh Dromedary and Bactrian Camels. [PDF]

Animals (Basel)
Niyazbekova Z, Gao CY, Makhanbetuly N, Kassen K, Xu Y, Baimirzayev B, Zhang H, Muslimova Z, Orynkhanov K, Ussenbekov Y, Bai F, Wang J, Baneh H, Serikov Y, Liu P, Jiang Y.   +15 more
europepmc   +1 more source

SHBG and APOA1 as serum biomarkers for low bone mineral density in Mexican postmenopausal women: a random forest-based analysis. [PDF]

Front Endocrinol (Lausanne)
Aparicio-Bautista DI, Becerra-Cervera A, Rivera-Paredez B, Jiménez-Ortega RF, López-Pérez TV, Salmerón J, Reyes-Grajeda JP, Hidalgo-Bravo A, Velázquez-Cruz R.   +8 more
europepmc   +1 more source

Ryanodine Receptor Ca²⁺ Leak-Induced Redistribution of Ca²⁺ in Dystrophic mdx Mouse Muscle. [PDF]

Acta Physiol (Oxf)
Gaglianone RB, Lamboley CR, Dick T, Meizoso-Huesca A, Singh DP, Launikonis BS.   +5 more
europepmc   +1 more source

Lightning Strikes Twice in the Same Place: Mitochondrial Myopathy and Malignant Hyperthermia-A Case Report. [PDF]

Case Rep Neurol Med
de Melo RSES, Mitsunaga Júnior JK, da Silva AMS, Souza BW, Santos JM, Andrade PV, Oliveira ASB, Sobreira CFDR, Vainzof M, da Silva HCA.   +9 more
europepmc   +1 more source

Considerations for diverse RYR1 variants in malignant hyperthermia susceptible patients: a report of two cases. [PDF]

BMC Anesthesiol
Fang Y, Mei W, Bi J.
europepmc   +1 more source

Type-1 Ryanodine Receptor Plays an Important Role in Cardiac Hypertrophy and Heart Failure by Increasing Type-2 Ryanodine Receptor-Mediated Calcium Release. [PDF]

Int J Mol Sci
Wang YX, Santos EW, Mistretta S, Yuan Y, Singer HA, Sheu SS, Zheng YM.   +6 more
europepmc   +1 more source

Prime editing of RYR1 gene

*RYR1*-related myopathies, the most frequently diagnosed congenital myopathies, are characterized by skeletal muscle hypotonia and non-progressive or slowly progressive skeletal muscle weakness. *RYR1*-related myopathies are caused by mutations in the *RYR1* gene.
openaire   +1 more source

Managing Secondary Findings from Germline Pharmacogenomic Testing. [PDF]

J Pers Med
Lee YM, Kearney E, Kisor DF, Farrell CL.
europepmc   +1 more source

Ryanodine receptor 1 (RyR1) [PDF]

Science-Business eXchange, 2012
openaire   +1 more source