Nigel K Spurr

Nigel K Spurr

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Nigel K Spurr

Nigel K Spurr

Publications by authors named "Nigel K Spurr"

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Atypical CTSK transcripts and ARNT transcription read-through into CTSK.

Comp Funct Genomics 2005 ;6(5-6):268-76

Department of Discovery Genetics, GlaxoSmithKline Research and Development, New Frontiers Science Park, Harlow, UK.

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http://dx.doi.org/10.1002/cfg.483DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447513PMC
June 2010

Pharmacogenetic studies of epilepsy drugs: are we there yet?

Authors:
Nigel K Spurr

Trends Genet 2006 May 24;22(5):250-2. Epub 2006 Mar 24.

Genetics Research, GlaxoSmithKline R&D, New Medicines Research Centre, Stevenage, Herts, UK, SG1 2NY.

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http://dx.doi.org/10.1016/j.tig.2006.03.004DOI Listing
May 2006

Guidelines for conducting and reporting whole genome/large-scale association studies.

Hum Mol Genet 2005 Sep 21;14(17):2485-8. Epub 2005 Jul 21.

Design and Standards, GlaxoSmithKline, Research Triangle Park, NC, USA.

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http://dx.doi.org/10.1093/hmg/ddi252DOI Listing
September 2005

A single-nucleotide polymorphism tagging set for human drug metabolism and transport.

Nat Genet 2005 Jan 19;37(1):84-9. Epub 2004 Dec 19.

Department of Biology (Galton Lab), University College London, The Darwin Building, Gower Street, London WC1E 6BT, UK.

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http://www.nature.com/articles/ng1488
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http://dx.doi.org/10.1038/ng1488DOI Listing
January 2005

Characterization of common genetic variants in cathepsin K and testing for association with bone mineral density in a large cohort of perimenopausal women from Scotland.

J Bone Miner Res 2004 Jan;19(1):31-41

Department of Discovery Genetics, GlaxoSmithKline Research and Development, New Frontiers Science Park, Harlow, United Kingdom.

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http://dx.doi.org/10.1359/JBMR.0301205DOI Listing
January 2004

Genetics of calcium-sensing--regulation of calcium levels in the body.

Authors:
Nigel K Spurr

Curr Opin Pharmacol 2003 Jun;3(3):291-4

Discovery Genetics, GlaxoSmithKline, Five Moore Drive, PO Box 13398, Research Triangle Park, NC 27709, USA.

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June 2003

A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.

J Neurosci 2003 Mar;23(5):1631-7

Medical Research Council Functional Genetics Unit, Department of Human Anatomy and Genetics, University of Oxford, Oxford OX1 3QX, United Kingdom.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741966PMC
March 2003

Molecular genetics of calcium sensing in bone cells.

Hum Mol Genet 2002 Oct;11(20):2377-84

Discovery Genetics, GlaxoSmithKline, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK.

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http://dx.doi.org/10.1093/hmg/11.20.2377DOI Listing
October 2002