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Träfflista för sökning "WFRF:(Robinson A. P. L.) srt2:(2000-2004)"

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1.	Adcox, K, et al. (author) PHENIX detector overview 2003 In: Nuclear Instruments & Methods in Physics Research. Section A: Accelerators, Spectrometers, Detectors, and Associated Equipment. - 0167-5087. ; 499:2-3, s. 469-479 Journal article (peer-reviewed)abstract The PHENIX detector is designed to perform a broad study of A-A, p-A, and p-p collisions to investigate nuclear matter under extreme conditions. A wide variety of probes, sensitive to all timescales, are used to study systematic variations with species and energy as well as to measure the spin structure of the nucleon. Designing for the needs of the heavy-ion and polarized-proton programs has produced a detector with unparalleled capabilities. PHENIX measures electron and muon pairs, photons, and hadrons with excellent energy and momentum resolution. The detector consists of a large number of subsystems that are discussed in other papers in this volume. The overall design parameters of the detector are presented. (C) 2002 Elsevier Science B.V. All rights reserved.
2.	Villablanca, A, et al. (author) Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP) 2004 In: Journal of medical genetics. - : BMJ. - 1468-6244. ; 41:3, s. e32- Journal article (peer-reviewed)
3.	Villablanca, A, et al. (author) Germline HRPT2 mutations in familial isolated hyperparathyroidism (FIHP) and in the hyperparathyroidism-jaw tumour syndrome (HPT-JT) 2004 In: JOURNAL OF INTERNAL MEDICINE. - 0954-6820. ; 255:6, s. 716-716 Conference paper (other academic/artistic)
4.	Robinson, R, et al. (author) Several interacting genes influence the malignant hyperthermia phenotype 2003 In: Human Genetics. - : Springer Science and Business Media LLC. - 1432-1203 .- 0340-6717. ; 112:2, s. 217-218 Journal article (peer-reviewed)abstract Malignant hyperthermia (MH), a potentially lethal disorder of skeletal muscle calcium homeostasis, manifests only on exposure to certain anaesthetic drugs. The mode of inheritance appears to be autosomal dominant with both locus and allelic heterogeneity having been reported. Association analysis of eight MH candidate loci in UK families has indicated that several genes influence susceptibility in individual families, rather than MH simply being a major gene defect. In support of this hypothesis, we present data on a replica analysis of an independent sample of European MH families.

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Type of publication: journal article (3); conference paper (1)

Type of content: peer-reviewed (3); other academic/artistic (1)

Author/Editor: Garpman, Sten (1); Gustafsson, Hans-Åke (1); Nilsson, Pål (1); Nystrand, Joakim (1); Oskarsson, Anders (1); Österman, Lennart (1); show more...; Otterlund, Ingvar (1); Silvermyr, David (1); Stenlund, Evert (1); Tydesjö, Henrik (1); Liu, X (1); Arai, Y. (1); Jia, J. (1); Liu, Y. (1); Milov, A. (1); Nagasaka, Y. (1); Nakamura, T. (1); Steinberg, P. (1); Tojo, J. (1); Yang, Y. (1); Zhang, L. (1); Zhang, Z. (1); Harvey, A. (1); Lebedev, A. (1); Xu, N. (1); Smith, M. (1); Bathe, S. (1); Kim, HJ (1); Turner, G (1); Liu, Z. (1); Aphecetche, L. (1); Averbeck, R. (1); Baldisseri, A. (1); Berdnikov, Y. (1); Blume, C. (1); Borel, H. (1); Buesching, H. (1); Chujo, T. (1); Constantin, P. (1); Delagrange, H. (1); Enokizono, A. (1); Gadrat, S. (1); Glenn, A. (1); Hamagaki, H. (1); Inaba, M. (1); Klein-Boesing, C. (1); Kwon, Y. (1); Mao, Y. (1); Miake, Y. (1); Newby, J. (1); show less...

University: Lund University (2); Karolinska Institutet (2)

Language: English (4)

Research subject (UKÄ/SCB): Natural sciences (1); Medical and Health Sciences (1)

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