Genetic variation in RYR1 and malignant hyperthermia phenotypes von Carpenter, D., Robinson, R.L., Quinnell, R.J., Ringrose, C., Hogg, M., Casson, F., Booms, P., Iles, D.E., Halsall, P.J., Steele, D.S., Shaw, M.-A., Hopkins, P.M.

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Epigenetic allele silencing and variable penetrance of malignant hyperthermia susceptibility von Robinson, R.L., Carpenter, D., Halsall, P.J., Iles, D.E., Booms, P., Steele, D., Hopkins, P.M., Shaw, M.-A.

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Multiple interacting gene products may influence susceptibility to malignant hyperthermia von ROBINSON, R. L., CURRAN, J. L., ELLIS, F. R., HALSALL, P. J., HALL, W. J., HOPKINS, P. M., ILES, D. E., WEST, S. P., SHAW, M-A.

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Segregation of malignant hyperthermia, central core disease and chromosome 19 markers von Curran, J L, Hall, W J, Halsall, P J, Hopkins, P M, Iles, D E, Markham, A F, McCall, S H, Robinson, R L, West, S P, Bridges, L R, Ellis, F R

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Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart von Schultz, D, Mikala, G, Yatani, A, Engle, D B, Iles, D E, Segers, B, Sinke, R J, Weghuis, D O, Klöckner, U, Wakamori, M

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The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree von ADEOKUN, A. M, WEST, S. P, ELLIS, F. R, HALSALL, P. J, HOPKINS, P. M, FOROUGHMAND, A. M, ILES, D. E, ROBINSON, R. L, STEWART, A. D, CURRAN, J. L

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Refined genetic localization for central core disease von MULLEY, J. C, KOZMAN, H. M, HAAN, E. A, PHILLIPS, H. A, GEDEON, A. K, MCCURE, J. A, ILES, D. E, GREGG, R. G, HOGAN, K, COUCH, F. J, MACLENNAN, D. H

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High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two mal... von Iles, D.E., Segers, B., Heytens, L., Sengers, R.C.A., Wieringa, B.

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Hemoxygenase-2 Is an Oxygen Sensor for a Calcium-Sensitive Potassium Channel von Williams, Sandile E. J, Wootton, Phillippa, Mason, Helen S, Bould, Jonathan, Iles, David E, Riccardi, Daniela, Peers, Chris, Kemp, Paul J

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Anesthesiologic problems in Williams syndrome : the CACNL2A locus is not involved von MAMMI, I, ILES, D. E, SMEETS, D, CLEMENTI, M, TENCONI, R

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Multipoint Mapping of the Central Core Disease Locus von Schwemmle, S., Wolff, K., Palmucci, L.M., Grimm, T., Lehmann-Horn, F., Hübner, Ch, Hauser, E., Iles, D.E., MacLennan, D.H., Müller, C.R.

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Properties of three COOH-terminal splice variants of a human cardiac L-type Ca2+-channel alpha1-subunit von Klockner, U, Mikala, G, Eisfeld, J, Iles, D. E, Strobeck, M, Mershon, J. L, Schwartz, A, Varadi, G

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Trinucleotide repeat polymorphism at the D19S190 locus von lles, David E., Segers, Bart, Jong, Pieter de, Alleman, Jennifer, Wieringa, Beé

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Localization of the gene encoding the α2/δ-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignan... von Iles, D.E., Lehmann-Horn, F., Scherer, S.W., Tsui, L.-C., Weghuis, D.Olde, Suijkerbuijk, R.F., Heytens, L., Mikala, G., Schwartz, A., Ellis, F.R., Stewart, A.D., Deufel, T., Wieringa, B.

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Dinucleotide repeat polymorphism at the D19S191 locus von lles, David E., Segers, Bart, Jong, Pieter de, Alleman, Jennifer, Wieringa, Beé

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Cloning, Chromosomal Localization, and Functional Expression of the α1Subunit of the L-Type Voltage-Dependent Calcium Channel from Normal Human Heart von Schultz, David, Mikala, Gabor, Yatani, Atsuko, Engle, Dorothy B., Iles, David E., Segers, Bart, Sinke, Richard J., Weghuis, Daniel Olde, Klockner, Udo, Wakamori, Minoru, Wang, Jing-Jing, Melvin, David, Varadi, Gyula, Schwartz, Arnold

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siRNA knock-down of γ-glutamyl transpeptidase does not affect hypoxic K + channel inhibition von Williams, Sandile E, Wootton, Phillippa, Mason, Helen S, Iles, David E, Peers, C, Kemp, Paul J

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Improving Management of Osteoporosis Through Simple Changes in Reporting Fragility Fractures von Burrell, Steven, MD, FRCPC, Frame, Heather, MD, FCPC, Ganguli, S. Nimu, MD, FRCPC, Iles, Sian E., MD FRCPC, Khan, Aliya, MD, FRCPC, FACP, FACE

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Properties of three COOH-terminal splice variants of a human cardiac L-type Ca2+-channel alpha1-subunit von Klockner, U, Mikala, G, Eisfeld, J, Iles, D E

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Properties of three COOH-terminal splice variants of a human cardiac L-type Ca2+-channel α1-subunit von KLÖCKNER, U, MIKALA, G, EISFELD, J, ILES, D. E, STROBECK, M, MERSHON, J. L, SCHWARTZ, A, VARADI, G

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