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157 related items for PubMed ID: 1354642
1. Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor (RYR1) gene in individuals with malignant hyperthermia. Gillard EF, Otsu K, Fujii J, Duff C, de Leon S, Khanna VK, Britt BA, Worton RG, MacLennan DH. Genomics; 1992 Aug; 13(4):1247-54. PubMed ID: 1354642 [Abstract] [Full Text] [Related]
2. The role of the skeletal muscle ryanodine receptor gene in malignant hyperthermia. MacLennan DH, Otsu K, Fujii J, Zorzato F, Phillips MS, O'Brien PJ, Archibald AL, Britt BA, Gillard EF, Worton RG. Symp Soc Exp Biol; 1992 Aug; 46():189-201. PubMed ID: 1341035 [Abstract] [Full Text] [Related]
12. A simple method to detect the RYR1 mutation G1021A, a cause of malignant hyperthermia susceptibility. Alestrøm A, Fagerlund TH, Berg K. Clin Genet; 1995 May; 47(5):274-5. PubMed ID: 7554356 [Abstract] [Full Text] [Related]
13. Detection of a novel RYR1 mutation in four malignant hyperthermia pedigrees. Keating KE, Quane KA, Manning BM, Lehane M, Hartung E, Censier K, Urwyler A, Klausnitzer M, Muller CR, Heffron JJ. Hum Mol Genet; 1994 Oct; 3(10):1855-8. PubMed ID: 7849712 [Abstract] [Full Text] [Related]
18. Identification of heterozygous and homozygous individuals with the novel RYR1 mutation Cys35Arg in a large kindred. Lynch PJ, Krivosic-Horber R, Reyford H, Monnier N, Quane K, Adnet P, Haudecoeur G, Krivosic I, McCarthy T, Lunardi J. Anesthesiology; 1997 Mar; 86(3):620-6. PubMed ID: 9066328 [Abstract] [Full Text] [Related]