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Nigel Spurr

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TOP 3
Nigel K Spurr
Pharmacogenetic studies of epilepsy drugs: are we there yet?
Margaret G Ehm; Matthew Nelson; Nigel K Spurr
Guidelines for conducting and reporting whole genome/large-scale association studies.
Fabienne S Giraudeau; Jean-Philippe Walhin; Paul R Murdock; Nigel K Spurr; Ian C Gray
Atypical CTSK transcripts and ARNT transcription read-through into CTSK.

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All Publications

2006: Nigel K Spurr
Pharmacogenetic studies of epilepsy drugs: are we there yet?
Trends in genetics : TIG 2006;22(5):250-2.
2005: Margaret G Ehm; Matthew Nelson; Nigel K Spurr
Guidelines for conducting and reporting whole genome/large-scale association studies.
Human molecular genetics 2005;14(17):2485-8.
2005: Fabienne S Giraudeau; Jean-Philippe Walhin; Paul R Murdock; Nigel K Spurr; Ian C Gray
Atypical CTSK transcripts and ARNT transcription read-through into CTSK.
Comparative and functional genomics 2005;6(5-6):268-76.
2005: Kourosh R Ahmadi; Michael E Weale; Zhengyu Y Xue; Nicole Soranzo; David P Yarnall; James D Briley; Yuka Maruyama; Mikiro Kobayashi; Nicholas W Wood; Nigel K Spurr; Daniel K Burns; Allen D Roses; Ann M Saunders; David B Goldstein
A single-nucleotide polymorphism tagging set for human drug metabolism and transport.
Nature genetics 2005;37(1):84-9.
2004: Mohamed Mohideen Quwailid; Alison Hugill; Neil Dear; Lucie Vizor; Sara Wells; Emma Horner; Shelly Fuller; Jessica Weedon; Hamish McMath; Paul Woodman; David Edwards; David Campbell; Susan Rodger; Joanne Carey; Ann Roberts; Peter Glenister; Zuzanna Lalanne; Nick Parkinson; Emma L Coghill; Richard McKeone; Sam Cox; John Willan; Andy Greenfield; David A Keays; Saffron Brady; Nigel K Spurr; Ian C Gray; Jackie Hunter; Steve D M Brown; Roger D Cox
A gene-driven ENU-based approach to generating an allelic series in any gene.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(8):585-91.
2004: Ayo TOYE; Lee Moir; Alison Hugill; Liz Bentley; Julie Quarterman; Vesna Mijat; Tertius A Hough; Michelle Goldsworthy; Alison Haynes; A Jackie Hunter; Mick Browne; Nigel K Spurr; Roger D Cox
A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.
Diabetes 2004;53(6):1577-83.
2004: Vicky Tsipouri; John A Curtin; Pat M Nolan; Lucie Vizor; Claire A Parsons; Colin M Clapham; Ian D Latham; Lesley J Rooke; Jo E Martin; Jo Peters; A Jackie Hunter; Derek Rogers; Sohaila Rastan; Steve D M Brown; Elizabeth M C Fisher; Nigel K Spurr; Ian C Gray
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.
Comparative and functional genomics 2004;5(2):123-7.
2004: Fabienne S Giraudeau; Ralph E McGinnis; Ian C Gray; Eamonn J O'Brien; Kim E Doncaster; Nigel K Spurr; Stuart H Ralston; David M Reid; John Wood
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.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2004;19(1):31-41.
2004: Theodore M Danoff; D A Campbell; Linda C McCarthy; K F Lewis; M H Repasch; Ann M Saunders; Nigel K Spurr; Ian Purvis; Allen D Roses; Chun-Fang Xu
A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia.
The pharmacogenomics journal 2004;4(1):49-53.
2003: Charlotte R Rhodes; Nick Parkinson; Hsun Tsai; Debra Brooker; Siobhan Mansell; Nigel K Spurr; A Jackie Hunter; Karen P Steel; Steve D M Brown
The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon.
Journal of neurocytology 2003;32(9):1143-54.
2003: John A Curtin; Elizabeth Quint; Vicky Tsipouri; Ruth Arkell; Bruce Cattanach; Andrew J Copp; Deborah J Henderson; Nigel K Spurr; Philip Stanier; Elizabeth M C Fisher; Patrick M Nolan; Karen P Steel; Steve D M Brown; Ian C Gray; Jennifer N Murdoch
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.
Current biology : CB 2003;13(13):1129-33.
2003: Nigel K Spurr
Genetics of calcium-sensing--regulation of calcium levels in the body.
Current opinion in pharmacology 2003;3(3):291-4.
2003: Hongxia Xu; Michael Y Sha; Edith Y Wong; Janet Uphoff; Yanzhang Xu; Joseph A Treadway; Anh Truong; Eamonn O'Brien; Steven Asquith; Michael Stubbins; Nigel K Spurr; Eric H Lai; Walt Mahoney
Multiplexed SNP genotyping using the Qbead system: a quantum dot-encoded microsphere-based assay.
Nucleic acids research 2003;31(8):e43.
2003: Adrian M Isaacs; Peter L Oliver; Emma L Jones; Alexander Jeans; Allyson Potter; Berit H Hovik; Patrick M Nolan; Lucie Vizor; Peter Glenister; A Katharina Simon; Ian C Gray; Nigel K Spurr; Steve D M Brown; A Jackie Hunter; Kay E Davies
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2003;23(5):1631-7.
2002: Ana M Valdes; Megan L Wolfe; Eamonn J O'Brien; Nigel K Spurr; Warren B Gefter; Andrew Rut; Pieter Groot; Daniel J Rader
Val64Ile polymorphism in the C-C chemokine receptor 2 is associated with reduced coronary artery calcification.
Arteriosclerosis, thrombosis, and vascular biology 2002;22(11):1924-8.
2002: Tertius A Hough; Patrick M Nolan; Vicky Tsipouri; Ayo TOYE; Ian C Gray; Michelle Goldsworthy; Lee Moir; Roger D Cox; Sian Clements; Peter Glenister; John Wood; Rachael L Selley; Mark A Strivens; Lucie Vizor; Stefan L McCormack; Josephine Peters; Elizabeth M C Fisher; Nigel K Spurr; Sohaila Rastan; Joanne E Martin; Steve D M Brown; A Jackie Hunter
Novel phenotypes identified by plasma biochemical screening in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(10):595-602.
2002: Jesús Purroy; Nigel K Spurr
Molecular genetics of calcium sensing in bone cells.
Human molecular genetics 2002;11(20):2377-84.
2001: Ralph E McGinnis; H Fox; P Yates; L A Cameron; Michael R Barnes; Ian C Gray; Nigel K Spurr; O Hurko; D St Clair
Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland.
Nature genetics 2001;28(2):128-9.
2000: M W Fear; David P Kelsell; Nigel K Spurr; Michael R Barnes
Wnt-16a, a novel Wnt-16 isoform, which shows differential expression in adult human tissues.
Biochemical and biophysical research communications 2000;278(3):814-20.
2000: Ian C Gray; D A Campbell; Nigel K Spurr
Single nucleotide polymorphisms as tools in human genetics.
Human molecular genetics 2000;9(16):2403-8.
2000: Adrian M Isaacs; Kay E Davies; A Jackie Hunter; Patrick M Nolan; Lucie Vizor; Jo Peters; D G Gale; David P Kelsell; I D Latham; J M Chase; Elizabeth M C Fisher; MM Bouzyk; Allyson Potter; M Masih; Frank S Walsh; M A Sims; K E Doncaster; C A Parsons; J Martin; Steve D M Brown; Sohaila Rastan; Nigel K Spurr; Ian C Gray
Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.
Human molecular genetics 2000;9(12):1865-71.
2000: Patrick M Nolan; Jo Peters; Lucie Vizor; Mark A Strivens; R Washbourne; Tertius A Hough; C Wells; Peter Glenister; C Thornton; J Martin; E Fisher; D Rogers; J Hagan; Charlie Reavill; Ian C Gray; John Wood; Nigel K Spurr; M Browne; Sohaila Rastan; Jackie Hunter; Steve D M Brown
Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(7):500-6.
2000: M A Sims; S D Field; M R Barnes; N Shaikh; K Ellington; K E Murphy; Nigel K Spurr; D A Campbell
Cloning and characterisation of ITGAV, the genomic sequence for human cell adhesion protein (vitronectin) receptor alpha subunit, CD51.
Cytogenetics and cell genetics 2000;89(3-4):268-71.
1999: Nigel K Spurr; A Darvasi; J Terrett; L Jazwinska
New technologies and DNA resources for high throughput biology.
British medical bulletin 1999;55(2):309-24.
1998: Ian C Gray; LM Stewart; S M Phillips; J A Hamilton; N E Gray; Graham J Watson; Nigel K Spurr; David Snary
Mutation and expression analysis of the putative prostate tumour-suppressor gene PTEN.
British journal of cancer 1998;78(10):1296-300.
1998: Carlo Nobile; Antonella Manca; Marina Pisano; Andrea Angius; Ian C Gray; Nigel K Spurr
A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(10):835-7.
1998: S Guioli; K Schmitt; Ricky Critcher; MM Bouzyk; Nigel K Spurr; T Ogata; J J Hoo; L Pinsky; G Gimelli; L Pasztor; PN Goodfellow
Molecular analysis of 9p deletions associated with XY sex reversal: refining the localization of a sex-determining gene to the tip of the chromosome.
American journal of human genetics 1998;63(3):905-8.
1998: S Ford; Ian C Gray; Nigel K Spurr
Rearrangement of the long arm of chromosome 10 in the prostate adenocarcinoma cell line LNCaP.
Cancer genetics and cytogenetics 1998;102(1):6-11.
1997: Linda C McCarthy; J Terrett; Maria E Davis; C J Knights; Angela L Smith; Ricky Critcher; K Schmitt; J Hudson; Nigel K Spurr; PN Goodfellow
A first-generation whole genome-radiation hybrid map spanning the mouse genome.
Genome research 1997;7(12):1153-61.
1997: J A White; P J McAlpine; S Antonarakis; H Cann; Janan T Eppig; Kenneth S Frazer; J Frezal; D Lancet; J Nahmias; P Pearson; J Peters; Alan F Scott; H Scott; Nigel K Spurr; C Conover Talbot; Sue Povey
Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee.
Genomics 1997;45(2):468-71.
1997: Antonella Manca; EV Volpi; F Laficara; Rosella Muresu; Ian C Gray; Nigel K Spurr; Carlo Nobile
Detailed physical analysis of a 1.5-megabase YAC contig containing the MXI1 and ADRA2A genes.
Genomics 1997;45(2):407-11.
1997: MM Bouzyk; SP Bryant; C Evans; S Guioli; S Ford; K Schmidt; PN Goodfellow; Sue Povey; M Rebello; S Rousseaux; Nigel K Spurr
Integrated radiation hybrid and yeast artificial chromosome map of chromosome 9p.
European journal of human genetics : EJHG 1997;5(5):299-307.
1997: Ian C Gray; J Fallowfield; S Ford; Carlo Nobile; EV Volpi; Nigel K Spurr
An integrated physical and genetic map spanning chromosome band 10q24.
Genomics 1997;43(1):85-8.
1997: Sue Povey; J Attwood; BP Chadwick; J Frezal; Jonathan L Haines; M Knowles; D J Kwiatkowski; O I Olopade; Susan A Slaugenhaupt; Nigel K Spurr; M Smith; K Steel; J A White; Margaret Pericak-Vance
Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996.
Annals of human genetics 1997;61(Pt 3):183-206.
1997: D Shimron-Abarbanell; Jeanette Erdmann; Ina R Vogt; SP Bryant; Nigel K Spurr; Michael Knapp; Peter Propping; Markus M Nöthen
Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region.
Biochemical and biophysical research communications 1997;233(1):6-9.
1997: Jürgen Deckert; Markus M Nöthen; SP Bryant; S Schuffenhauer; P R Schofield; Nigel K Spurr; Peter Propping
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region.
Human genetics 1997;99(3):326-8.
1997: Michael Jones; Y Zhang; K N Tirosvoutis; P M Davey; AR Webster; D Walsh; Nigel K Spurr; Nabeel A Affara
Chromosomal assignment of 311 sequences transcribed in human adult testis.
Genomics 1997;40(1):155-67.
1997: Chun-Fang Xu; JA Chambers; Hans Nicolai; Melissa A Brown; Y Hujeirat; S Mohammed; Shirley Hodgson; David P Kelsell; Nigel K Spurr; Tim BISHOP; Ellen Solomon
Mutations and alternative splicing of the BRCA1 gene in UK breast/ovarian cancer families.
Genes, chromosomes & cancer 1997;18(2):102-10.
1997: E Mavraki; Ian C Gray; Tim BISHOP; Nigel K Spurr
Germline BRCA2 mutations in men with breast cancer.
British journal of cancer 1997;76(11):1428-31.
1996: S A Cox; J Attwood; S P Bryant; R Bains; S Povey; M Rebello; Manuela Kapsetaki; Nicholas K Moschonas; K H Grzeschik; M Otto; M Dixon; H E Sudworth; R Frank Kooy; A Wright; P Teague; L Terrenato; Gilles Vergnaud; S Monfouilloux; Jean Weissenbach; O Alibert; C Dib; S Fauré; E Bakker; N M Pearson; Nigel K Spurr
European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme Humain.
Annals of human genetics 1996;60(Pt 6):447-86.
1996: Frances J D Smith; Robin A J Eady; Irene M Leigh; James R McMillan; Elizabeth L Rugg; David P Kelsell; S P Bryant; Nigel K Spurr; J F Geddes; Gudula Kirtschig; G Milana; A G de Bono; Katsushi Owaribe; Gerhard Wiche; L Pulkkinen; J Uitto; W H Irwin McLean; E Birgitte Lane
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa.
Nature genetics 1996;13(4):450-7.
1996: G Dewald; Sven Cichon; S P Bryant; S Hemmer; Markus M Nöthen; Nigel K Spurr
The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.
Annals of human genetics 1996;60(Pt 4):281-91.
1996: David P Kelsell; Janet M Risk; Irene M Leigh; Howard P Stevens; A Ellis; Hans Christian Hennies; André Reis; Jean Weissenbach; D Timothy Bishop; Nigel K Spurr; John Field
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).
Human molecular genetics 1996;5(6):857-60.
1996: M Bouzyk; S P Bryant; K Schmitt; PN Goodfellow; R Ekong; Nigel K Spurr
Construction of a radiation hybrid map of chromosome 9p.
Genomics 1996;34(2):187-92.
1996: Howard P Stevens; David P Kelsell; S P Bryant; D Timothy Bishop; Nigel K Spurr; Jean Weissenbach; D Marger; R S Marger; Irene M Leigh
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.
Archives of dermatology 1996;132(6):640-51.
1996: Howard P Stevens; David P Kelsell; S P Bryant; D Timothy Bishop; R P Dawber; Nigel K Spurr; Irene M Leigh
Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13.
The Journal of investigative dermatology 1996;106(4):795-7.
1996: M Bouzyk; C Evans; L Cullin; S Cox; D Warne; K Nyberg; S P Bryant; Nigel K Spurr
Isolation and mapping of three new polymorphic markers to chromosomes 3, 20 and 21.
Annals of human genetics 1996;60(Pt 1):73-7.
1996: C Evans; M Bouzyk; S Cox; D Warne; S P Bryant; Nigel K Spurr
Chromosomal assignment of 79 cDNAs from a range of human tissues.
Genomics 1996;31(1):130-4.
1995: Nigel K Spurr; A C Gough; F I Chinegwundoh; C A Smith
Polymorphisms in drug-metabolizing enzymes as modifiers of cancer risk.
Clinical chemistry 1995;41(12 Pt 2):1864-9.
1995: S Cox; S P Bryant; ANDREW COLLINS; Jean Weissenbach; H Donis-Keller; B P Koeleman; Alexander Steinkasserer; Nigel K Spurr
Integrated genetic map of human chromosome 2.
Annals of human genetics 1995;59(Pt 4):413-34.
1995: Jürgen Deckert; Markus M Nöthen; S P Bryant; H Ren; H K Wolf; G L Stiles; Nigel K Spurr; Peter Propping
Human adenosine A1 receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 1q31-32.1 using a silent polymorphism in the coding region.
Biochemical and biophysical research communications 1995;214(2):614-21.
1995: Ian C Gray; Carlo Nobile; Rosella Muresu; S Ford; Nigel K Spurr
A 2.4-megabase physical map spanning the CYP2C gene cluster on chromosome 10q24.
Genomics 1995;28(2):328-32.
1995: David P Kelsell; Howard P Stevens; R Ratnavel; S P Bryant; D Timothy Bishop; Irene M Leigh; Nigel K Spurr
Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity.
Human molecular genetics 1995;4(6):1021-5.
1995: D P Kelsell; L Rooke; D Warne; M Bouzyk; L Cullin; S Cox; L West; S Povey; Nigel K Spurr
Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping.
Annals of human genetics 1995;59(Pt 2):233-41.
1995: C MacGeoch; G Turner; L G Bobrow; DM Barnes; Tim BISHOP; Nigel K Spurr
Heterogeneity in Li-Fraumeni families: p53 mutation analysis and immunohistochemical staining.
Journal of medical genetics 1995;32(3):186-90.
1994: PJ Townsend; H Farza; C MacGeoch; Nigel K Spurr; R Wade; R Gahlmann; M H Yacoub; Paul J R Barton
Human cardiac troponin T: identification of fetal isoforms and assignment of the TNNT2 locus to chromosome 1q.
Genomics 1994;21(2):311-6.
1994: H M Barker; N D Brewis; A J Street; Nigel K Spurr; Patricia T W Cohen
Three genes for protein phosphatase 1 map to different human chromosomes: sequence, expression and gene localisation of protein serine/threonine phosphatase 1 beta (PPP1CB).
Biochimica et biophysica acta 1994;1220(2):212-8.
1994: A C Gough; S Zhong; C Roland Wolf; Nigel K Spurr
Chromosome assignment of the human glutathione S-transferase mu 3 gene (GSTM3) to chromosome 1 by gene specific polymerase chain reaction.
Cytogenetics and cell genetics 1994;65(1-2):111-4.
1994: S A Cox; Nigel K Spurr; Gilles Vergnaud; Licinio Contu; Carlo Carcassi; T McCarthy
The EUROGEM map of human chromosome 8.
European journal of human genetics : EJHG 1994;2(3):218-9.
1994: Nigel K Spurr; S P Bryant; J Attwood; K Nyberg; S A Cox; A Mills; R Bains; D Warne; L Cullin; S Povey
European Gene Mapping Project (EUROGEM): genetic maps based on the CEPH reference families.
European journal of human genetics : EJHG 1994;2(3):193-203.
1993: C MacGeoch; DM Barnes; J A Newton; S Mohammed; S V Hodgson; M Ng; Tim BISHOP; Nigel K Spurr
p53 protein detected by immunohistochemical staining is not always mutant.
Disease markers 1993;11(5-6):239-50.
1993: H M Barker; S P Craig; Nigel K Spurr; Patricia T W Cohen
Sequence of human protein serine/threonine phosphatase 1 gamma and localization of the gene (PPP1CC) encoding it to chromosome bands 12q24.1-q24.2.
Biochimica et biophysica acta 1993;1178(2):228-33.
1993: D P Kelsell; D M Black; E Solomon; Nigel K Spurr
Localization of a second NM23 gene, NME2, to chromosome 17q21-q22.
Genomics 1993;17(2):522-4.
1993: A C Gough; C A Smith; S M Howell; C Roland Wolf; S P Bryant; Nigel K Spurr
Localization of the CYP2D gene locus to human chromosome 22q13.1 by polymerase chain reaction, in situ hybridization, and linkage analysis.
Genomics 1993;15(2):430-2.
1993: T A Jones; H M Barker; E F da Cruz e Silva; R E Mayer-Jaekel; B A Hemmings; Nigel K Spurr; Denise Sheer; Patricia T W Cohen
Localization of the genes encoding the catalytic subunits of protein phosphatase 2A to human chromosome bands 5q23-->q31 and 8p12-->p11.2, respectively.
Cytogenetics and cell genetics 1993;63(1):35-41.
1993: Nigel K Spurr; S Cox; Susan Naylor
Report and abstracts of the Second International Workshop on Human Chromosome 2 Mapping.
Cytogenetics and cell genetics 1993;64(2):69-92.
1992: S Zhong; C Roland Wolf; Nigel K Spurr
Chromosomal assignment and linkage analysis of the human glutathione S-transferase mu gene (GSTM1) using intron specific polymerase chain reaction.
Human genetics 1992;90(4):435-9.
1992: Nigel K Spurr; S Cox; S P Bryant; J Attwood; E B Robson; D C Shields; T Steinbrueck; T Jenkins; J C Murray; K K Kidd
The CEPH consortium linkage map of human chromosome 2.
Genomics 1992;14(4):1055-63.
1992: C A Smith; J E Moss; A C Gough; Nigel K Spurr; C Roland Wolf
Molecular genetic analysis of the cytochrome P450-debrisoquine hydroxylase locus and association with cancer susceptibility.
Environmental health perspectives 1992;98():107-12.
1992: K Ridgwell; Nigel K Spurr; B Laguda; C MacGeoch; Neil D Avent; Michael Tanner
Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression.
The Biochemical journal 1992;287 ( Pt 1)():223-8.
1992: C Roland Wolf; C A Smith; G Smith; A C Gough; S Bryant; Nigel K Spurr; D J Harrison
Molecular genetics of the human cytochrome P450-dependent monooxygenases.
The Tohoku journal of experimental medicine 1992;168(2):73-81.
1992: DM Barnes; Andrew M Hanby; Cheryl E Gillett; S Mohammed; Shirley Hodgson; LG Bobrow; I M Leigh; T Purkis; C MacGeoch; Nigel K Spurr
Abnormal expression of wild type p53 protein in normal cells of a cancer family patient.
Lancet 1992;340(8814):259-63.
1992: P Bodfish; D Warne; K Nyberg; Nigel K Spurr
Dinucleotide repeat polymorphism at the human erythroid alpha-spectrin (SPTA1) mRNA gene detected using PCR.
Human molecular genetics 1992;1(4):287.
1992: Nigel K Spurr
Standards for reporting alleles at highly polymorphic loci: a proposal.
Human molecular genetics 1992;1(3):211-2.
1992: Deborah E Barnes; K Kodama; K Tynan; B J Trask; M Christensen; P J De Jong; Nigel K Spurr; Tomas Lindahl; Harvey W Mohrenweiser
Assignment of the gene encoding DNA ligase I to human chromosome 19q13.2-13.3.
Genomics 1992;12(1):164-6.
1992: C MacGeoch; C J Mitchell; B Carritt; Neil D Avent; K Ridgwell; Michael Tanner; Nigel K Spurr
Assignment of the chromosomal locus of the human 30-kDal Rh (rhesus) blood group-antigen-related protein (Rh30A) to chromosome region 1p36.13----p34.
Cytogenetics and cell genetics 1992;59(4):261-3.
1991: D Warne; C Watkins; P Bodfish; K Nyberg; Nigel K Spurr
Tetranucleotide repeat polymorphism at the human beta-actin related pseudogene 2 (ACTBP2) detected using the polymerase chain reaction.
Nucleic acids research 1991;19(24):6980.
1991: C Watkins; P Bodfish; D Warne; K Nyberg; Nigel K Spurr
Dinucleotide repeat polymorphism in the human alpha-cardiac actin gene, intron IV (ACTC), detected using the polymerase chain reaction.
Nucleic acids research 1991;19(24):6980.
1991: P Bodfish; D Warne; C Watkins; K Nyberg; Nigel K Spurr
Dinucleotide repeat polymorphism in the human coagulation factor XI gene, intron B (F11), detected using the polymerase chain reaction.
Nucleic acids research 1991;19(24):6979.
1991: C MacGeoch; Paul J R Barton; W J Vallins; P Bhavsar; Nigel K Spurr
The human cardiac troponin I locus: assignment to chromosome 19p13.2-19q13.2.
Human genetics 1991;88(1):101-4.
1991: S M Howell; H V Molgaard; M F Greaves; Nigel K Spurr
Localisation of the gene coding for the haemopoietic stem cell antigen CD34 to chromosome 1q32.
Human genetics 1991;87(5):625-7.
1991: S Zhong; A F Howie; B Ketterer; J Taylor; J D Hayes; G J Beckett; C G Wathen; C R Wolf; Nigel K Spurr
Glutathione S-transferase mu locus: use of genotyping and phenotyping assays to assess association with lung cancer susceptibility.
Carcinogenesis 1991;12(9):1533-7.
1991: Nigel K Spurr; L Rooke
Confirmation of the assignment of the vitronectin (VNRA) and fibronectin (FNRA) receptor alpha-subunits.
Annals of human genetics 1991;55(Pt 3):217-23.
1991: Nigel K Spurr; D Kelsell; L Rooke; L L Cavalli-Sforza; A Bowcock; J Feder
Assignment of eight human genomic DNA sequences detecting high frequency restriction fragment length polymorphisms.
Annals of human genetics 1991;55(Pt 2):141-50.
1991: C Roland Wolf; J E Moss; J S Miles; A C Gough; Nigel K Spurr
Prediction of debrisoquine phenotype.
Lancet 1991;337(8741):623.
1990: C Roland Wolf; J E Moss; J S Miles; A C Gough; Nigel K Spurr
Detection of debrisoquine hydroxylation phenotypes.
Lancet 1990;336(8728):1452-3.
1990: A C Gough; J S Miles; Nigel K Spurr; J E Moss; A Gaedigk; M Eichelbaum; C Roland Wolf
Identification of the primary gene defect at the cytochrome P450 CYP2D locus.
Nature 1990;347(6295):773-6.
1990: H M Barker; T A Jones; E F da Cruz e Silva; Nigel K Spurr; Denise Sheer; Patricia T W Cohen
Localization of the gene encoding a type I protein phosphatase catalytic subunit to human chromosome band 11q13.
Genomics 1990;7(2):159-66.
1990: T A Jones; E F da Cruz e Silva; Nigel K Spurr; Denise Sheer; Patricia T W Cohen
Localisation of the gene encoding the catalytic gamma subunit of phosphorylase kinase to human chromosome bands 7p12-q21.
Biochimica et biophysica acta 1990;1048(1):24-9.
1990: Nigel K Spurr; A C Gough; M G Lee
Cloning of the mouse homologue of the yeast cell cycle control gene cdc2.
DNA sequence : the journal of DNA sequencing and mapping 1990;1(1):49-54.
1989: Nigel K Spurr; C Mitchell; A C Gough; L Rooke; John Kenneth Cowell
Assignment of an anonymous DNA sequence IB/D22 (DXS371) to XP11.1-11.4.
Disease markers 1989;7(4):247-51.
1989: A C Gough; Nigel K Spurr; Richard Meehan; J S Miles; C Roland Wolf
An XmnI RFLP detected with a cDNA probe for the CYP2C gene locus on chromosome 10.
Nucleic acids research 1989;17(11):4426.
1989: Anne E Willis; Nigel K Spurr; Tomas Lindahl
Concomitant reversion of the characteristic phenotypic properties of a cell line of Bloom's syndrome origin.
Carcinogenesis 1989;10(1):217-9.
1989: Nigel K Spurr; A C Gough; K Stevenson; C R Wolf
The human cytochrome P450 CYP3 locus: assignment to chromosome 7q22-qter.
Human genetics 1989;81(2):171-4.
1988: J S Miles; Nigel K Spurr; A C Gough; T Jowett; Aileen W McLaren; J D Brook; C Roland Wolf
A novel human cytochrome P450 gene (P450IIB): chromosomal localization and evidence for alternative splicing.
Nucleic acids research 1988;16(13):5783-95.
1988: Nigel K Spurr; A Gough; Paul J Goodfellow; PN Goodfellow; M G Lee; Paul Nurse
Evolutionary conservation of the human homologue of the yeast cell cycle control gene cdc2 and assignment of Cd2 to chromosome 10.
Human genetics 1988;78(4):333-7.
1988: Nigel K Spurr; A C Gough; JR Gosden; D Rout; David J Porteous; Veronica van Heyningen; A J Docherty
Restriction fragment length polymorphism analysis and assignment of the metalloproteinases stromelysin and collagenase to the long arm of chromosome 11.
Genomics 1988;2(2):119-27.
1988: Nigel K Spurr; P N Goodfellow; P Johnson
CD8B, the human equivalent of the mouse Ly-3 gene is localized on chromosome 2.
Immunogenetics 1988;27(1):70-2.
1988: Richard Meehan; JR Gosden; D Rout; Nicholas D Hastie; T Friedberg; M Adesnik; R Buckland; Veronica van Heyningen; J Fletcher; Nigel K Spurr
Human cytochrome P-450 PB-1: a multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10.
American journal of human genetics 1988;42(1):26-37.
1987: Nigel K Spurr; A C Gough; K Stevenson; C R Wolf
Msp-1 polymorphism detected with a cDNA probe for the P-450 I family on chromosome 15.
Nucleic acids research 1987;15(14):5901.
1987: Nigel K Spurr; P N Goodfellow; A J Docherty
Chromosomal assignment of the gene encoding the human tissue inhibitor of metalloproteinases to Xp11.1-p11.4.
Annals of human genetics 1987;51(Pt 3):189-94.
1987: K Willison; A Kelly; K Dudley; P Goodfellow; Nigel K Spurr; V Groves; P Gorman; D Sheer; J Trowsdale
The human homologue of the mouse t-complex gene, TCP1, is located on chromosome 6 but is not near the HLA region.
The EMBO journal 1987;6(7):1967-74.
1987: D Martin; D F Tucker; P Gorman; Denise Sheer; Nigel K Spurr; J Trowsdale
The human placental alkaline phosphatase gene and related sequences map to chromosome 2 band q37.
Annals of human genetics 1987;51(Pt 2):145-52.
1986: Nigel K Spurr; J Feder; W F Bodmer; P N Goodfellow; Ellen Solomon; L L Cavalli-Sforza
Chromosomal assignment of seven human genomic DNA sequences associated with restriction fragment length polymorphisms.
Annals of human genetics 1986;50(Pt 2):145-52.
1985: T Seki; Nigel K Spurr; F Obata; Sanna Goyert; P Goodfellow; J Silver
The human Thy-1 gene: structure and chromosomal location.
Proceedings of the National Academy of Sciences of the United States of America 1985;82(19):6657-61.
1984: A J Jeffreys; V Wilson; A Blanchetot; P Weller; A Geurts van Kessel; Nigel K Spurr; E Solomon; P Goodfellow
The human myoglobin gene: a third dispersed globin locus in the human genome.
Nucleic acids research 1984;12(7):3235-43.