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Items: 31

1.

Silicon analogues of the nonpeptidic GnRH antagonist AG-045572: syntheses, crystal structure analyses, and pharmacological characterization.

Barnes MJ, Burschka C, B├╝ttner MW, Conroy R, Daiss JO, Gray IC, Hendrick AG, Tam LH, Kuehn D, Miller DJ, Mills JS, Mitchell P, Montana JG, Muniandy PA, Rapley H, Showell GA, Tebbe D, Tacke R, Warneck JB, Zhu B.

ChemMedChem. 2011 Nov 4;6(11):2070-80. doi: 10.1002/cmdc.201100318. Epub 2011 Sep 27.

PMID:
21953839
2.

CCR2 and coronary artery disease: a woscops substudy.

Dow DJ, McMahon AD, Gray IC, Packard CJ, Groot PH.

BMC Res Notes. 2010 Feb 2;3:31. doi: 10.1186/1756-0500-3-31.

3.

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

Giraudeau FS, Walhin JP, Murdock PR, Spurr NK, Gray IC.

Comp Funct Genomics. 2005;6(5-6):268-76. doi: 10.1002/cfg.483.

4.

Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.

Tsipouri V, Curtin JA, Nolan PM, Vizor L, Parsons CA, Clapham CM, Latham ID, Rooke LJ, Martin JE, Peters J, Hunter AJ, Rogers D, Rastan S, Brown SD, Fisher EM, Spurr NK, Gray IC.

Comp Funct Genomics. 2004;5(2):123-7. doi: 10.1002/cfg.382.

5.

Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders.

Rastan S, Hough T, Kierman A, Hardisty R, Erven A, Gray IC, Voeling S, Isaacs A, Tsai H, Strivens M, Washbourne R, Thornton C, Greenaway S, Hewitt M, McCormick S, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Mburu P, Rogers D, Hagan J, Reavill C, Davies K, Glenister P, Fisher EM, Martin J, Vizor L, Bouzyk M, Kelsell D, Guenet JL, Steel KP, Sheardown S, Spurr N, Gray I, Peters J, Nolan PM, Hunter AJ, Brown SD.

Genetica. 2004 Sep;122(1):47-9.

PMID:
15619960
6.

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.

Giraudeau FS, McGinnis RE, Gray IC, O'Brien EJ, Doncaster KE, Spurr NK, Ralston SH, Reid DM, Wood J.

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

7.

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.

Curtin JA, Quint E, Tsipouri V, Arkell RM, Cattanach B, Copp AJ, Henderson DJ, Spurr N, Stanier P, Fisher EM, Nolan PM, Steel KP, Brown SD, Gray IC, Murdoch JN.

Curr Biol. 2003 Jul 1;13(13):1129-33.

8.

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

Isaacs AM, Oliver PL, Jones EL, Jeans A, Potter A, Hovik BH, Nolan PM, Vizor L, Glenister P, Simon AK, Gray IC, Spurr NK, Brown SD, Hunter AJ, Davies KE.

J Neurosci. 2003 Mar 1;23(5):1631-7.

9.

Novel phenotypes identified by plasma biochemical screening in the mouse.

Hough TA, Nolan PM, Tsipouri V, Toye AA, Gray IC, Goldsworthy M, Moir L, Cox RD, Clements S, Glenister PH, Wood J, Selley RL, Strivens MA, Vizor L, McCormack SL, Peters J, Fisher EM, Spurr N, Rastan S, Martin JE, Brown SD, Hunter AJ.

Mamm Genome. 2002 Oct;13(10):595-602.

PMID:
12420138
10.

Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland.

McGinnis RE, Fox H, Yates P, Cameron LA, Barnes MR, Gray IC, Spurr NK, Hurko O, St Clair D.

Nat Genet. 2001 Jun;28(2):128-9.

PMID:
11381258
11.

Single nucleotide polymorphisms as tools in human genetics.

Gray IC, Campbell DA, Spurr NK.

Hum Mol Genet. 2000 Oct;9(16):2403-8. Review.

PMID:
11005795
12.

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.

Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson JA, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel KP, Voegeling S, Guenet JL, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher EM, Martin J, Rastan S, Brown SD, Hunter J.

Nat Genet. 2000 Aug;25(4):440-3.

PMID:
10932191
13.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.

Isaacs AM, Davies KE, Hunter AJ, Nolan PM, Vizor L, Peters J, Gale DG, Kelsell DP, Latham ID, Chase JM, Fisher EM, Bouzyk MM, Potter A, Masih M, Walsh FS, Sims MA, Doncaster KE, Parsons CA, Martin J, Brown SD, Rastan S, Spurr NK, Gray IC.

Hum Mol Genet. 2000 Jul 22;9(12):1865-71.

PMID:
10915775
14.

The expression profile for the tumour suppressor gene PTEN and associated polymorphic markers.

Hamilton JA, Stewart LM, Ajayi L, Gray IC, Gray NE, Roberts KG, Watson GJ, Kaisary AV, Snary D.

Br J Cancer. 2000 May;82(10):1671-6.

15.

Mutation and expression analysis of the putative prostate tumour-suppressor gene PTEN.

Gray IC, Stewart LM, Phillips SM, Hamilton JA, Gray NE, Watson GJ, Spurr NK, Snary D.

Br J Cancer. 1998 Nov;78(10):1296-300.

16.

A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders.

Nobile C, Manca A, Pisano M, Angius A, Gray IC, Spurr NK.

Mamm Genome. 1998 Oct;9(10):835-7. No abstract available.

PMID:
9745040
17.

Rearrangement of the long arm of chromosome 10 in the prostate adenocarcinoma cell line LNCaP.

Ford S, Gray IC, Spurr NK.

Cancer Genet Cytogenet. 1998 Apr 1;102(1):6-11.

PMID:
9530332
18.

Detailed physical analysis of a 1.5-megabase YAC contig containing the MXI1 and ADRA2A genes.

Manca A, Volpi EV, Laficara F, Muresu R, Gray IC, Spurr NK, Nobile C.

Genomics. 1997 Oct 15;45(2):407-11.

PMID:
9344667
19.

An integrated physical and genetic map spanning chromosome band 10q24.

Gray IC, Fallowfield J, Ford S, Nobile C, Volpi EV, Spurr NK.

Genomics. 1997 Jul 1;43(1):85-8.

PMID:
9226376
20.

Germline BRCA2 mutations in men with breast cancer.

Mavraki E, Gray IC, Bishop DT, Spurr NK.

Br J Cancer. 1997;76(11):1428-31.

21.

Loss of the chromosomal region 10q23-25 in prostate cancer.

Gray IC, Phillips SM, Lee SJ, Neoptolemos JP, Weissenbach J, Spurr NK.

Cancer Res. 1995 Nov 1;55(21):4800-3.

22.

A 2.4-megabase physical map spanning the CYP2C gene cluster on chromosome 10q24.

Gray IC, Nobile C, Muresu R, Ford S, Spurr NK.

Genomics. 1995 Jul 20;28(2):328-32.

PMID:
8530044
23.

Simple excision of the trapezium for osteoarthritis of the carpometacarpal joint of the thumb.

Dhar S, Gray IC, Jones WA, Beddow FH.

J Hand Surg Br. 1994 Aug;19(4):485-8.

PMID:
7964101
24.

Comminuted tibial fracture: an unusual stress fracture.

Gillies R, Gray IC.

Injury. 1992;23(5):345-6. No abstract available.

PMID:
1644474
25.

Identification of the skeletal remains of a murder victim by DNA analysis.

Hagelberg E, Gray IC, Jeffreys AJ.

Nature. 1991 Aug 1;352(6334):427-9.

PMID:
1861721
26.

Evolutionary transience of hypervariable minisatellites in man and the primates.

Gray IC, Jeffreys AJ.

Proc Biol Sci. 1991 Mar 22;243(1308):241-53.

PMID:
1675801
27.

Principles and recent advances in human DNA fingerprinting.

Jeffreys AJ, Royle NJ, Patel I, Armour JA, MacLeod A, Collick A, Gray IC, Neumann R, Gibbs M, Crosier M, et al.

EXS. 1991;58:1-19. Review.

PMID:
1831152
28.

Psychological assessment in general orthopaedic practice.

Gray IC, Main CJ, Waddell G.

Clin Orthop Relat Res. 1985 Apr;(194):258-63.

PMID:
3156707
29.
30.

Chronic low-back pain, psychologic distress, and illness behavior.

Waddell G, Main CJ, Morris EW, Di Paola M, Gray IC.

Spine (Phila Pa 1976). 1984 Mar;9(2):209-13.

PMID:
6233714
31.

Fine screen filtration of banked blood: effect on red cell survival.

Browning JD, Gray IC, Ledingham IM.

Br J Anaesth. 1980 Mar;52(3):299-304.

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