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Items: 1 to 50 of 217

1.

Evolution of the male-determining gene SRY within the cat family Felidae.

King V, Goodfellow PN, Pearks Wilkerson AJ, Johnson WE, O'Brien SJ, Pecon-Slattery J.

Genetics. 2007 Apr;175(4):1855-67. Epub 2007 Feb 4.

2.

Genomics and drugs. An interview conducted by Holger Breithaupt and Caroline Hadley.

Goodfellow PN.

EMBO Rep. 2004 Sep;5(9):843-6. No abstract available.

3.

A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility.

Sawcer S, Maranian M, Setakis E, Curwen V, Akesson E, Hensiek A, Coraddu F, Roxburgh R, Sawcer D, Gray J, Deans J, Goodfellow PN, Walker N, Clayton D, Compston A.

Brain. 2002 Jun;125(Pt 6):1337-47.

PMID:
12023322
4.

DAX-1, an "antitestis" gene.

Goodfellow PN, Camerino G.

EXS. 2001;(91):57-69. Review.

PMID:
11301600
5.

Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosis.

Chataway J, Sawcer S, Coraddu F, Feakes R, Broadley S, Jones HB, Clayton D, Gray J, Goodfellow PN, Compston A.

Neurogenetics. 1999 Apr;2(2):91-6.

PMID:
10369884
6.

The impact of genomics on drug discovery.

Goodfellow PN.

Novartis Found Symp. 2000;229:131-2; discussion 132-5. No abstract available.

PMID:
11084938
7.

A horse whole-genome-radiation hybrid panel: chromosome 1 and 10 preliminary maps.

Kiguwa SL, Hextall P, Smith AL, Critcher R, Swinburne J, Millon L, Binns MM, Goodfellow PN, McCarthy LC, Farr CJ, Oakenfull EA.

Mamm Genome. 2000 Sep;11(9):803-5. No abstract available.

PMID:
10967144
8.

A whole-genome radiation hybrid panel and framework map of the rat genome.

McCarthy LC, Bihoreau MT, Kiguwa SL, Browne J, Watanabe TK, Hishigaki H, Tsuji A, Kiel S, Webber C, Davis ME, Knights C, Smith A, Critcher R, Huxtall P, Hudson JR Jr, Ono T, Hayashi H, Takagi T, Nakamura Y, Tanigami A, Goodfellow PN, Lathrop GM, James MR.

Mamm Genome. 2000 Sep;11(9):791-5. No abstract available.

PMID:
10967141
9.

Impact of genomics on healthcare. Overview.

Goodfellow PN.

Br Med Bull. 1999;55(2):305-8. No abstract available.

PMID:
10723858
10.

No evidence for association of multiple sclerosis with the complement factors C6 and C7.

Chataway J, Sawcer S, Sherman D, Hobart M, Fernie B, Coraddu F, Feakes R, Broadley S, Gray J, Jones HB, Clayton D, Goodfellow PN, Compston A.

J Neuroimmunol. 1999 Sep 1;99(1):150-6.

PMID:
10496188
11.

A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosis.

Chataway J, Sawcer S, Feakes R, Coraddu F, Broadley S, Jones HB, Clayton D, Gray J, Goodfellow PN, Compston A.

J Neuroimmunol. 1999 Aug 3;98(2):208-13.

PMID:
10430054
12.

DAX-1, an 'antitestis' gene.

Goodfellow PN, Camerino G.

Cell Mol Life Sci. 1999 Jun;55(6-7):857-63. Review.

PMID:
10412368
13.

HLA typing in the United Kingdom multiple sclerosis genome screen.

Coraddu F, Sawcer S, Feakes R, Chataway J, Broadley S, Jones HB, Clayton D, Gray J, Smith S, Taylor C, Goodfellow PN, Compston A.

Neurogenetics. 1998 Dec;2(1):24-33.

PMID:
9933297
14.

Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosis.

Feakes R, Sawcer S, Chataway J, Coraddu F, Broadley S, Gray J, Jones HB, Clayton D, Goodfellow PN, Compston A.

Genet Epidemiol. 1999;17(1):51-63.

PMID:
10323184
15.

A radiation hybrid map of the rat genome containing 5,255 markers.

Watanabe TK, Bihoreau MT, McCarthy LC, Kiguwa SL, Hishigaki H, Tsuji A, Browne J, Yamasaki Y, Mizoguchi-Miyakita A, Oga K, Ono T, Okuno S, Kanemoto N, Takahashi E, Tomita K, Hayashi H, Adachi M, Webber C, Davis M, Kiel S, Knights C, Smith A, Critcher R, Miller J, Thangarajah T, Day PJ, Hudson JR Jr, Irie Y, Takagi T, Nakamura Y, Goodfellow PN, Lathrop GM, Tanigami A, James MR.

Nat Genet. 1999 May;22(1):27-36.

PMID:
10319858
16.

Characterisation and mapping of the human SOX14 gene.

Arsic N, Rajic T, Stanojcic S, Goodfellow PN, Stevanovic M.

Cytogenet Cell Genet. 1998;83(1-2):139-46.

PMID:
9925951
17.

DNA microarrays in drug discovery and development.

Debouck C, Goodfellow PN.

Nat Genet. 1999 Jan;21(1 Suppl):48-50. Review.

PMID:
9915501
18.

Inheritance of susceptibility to multiple sclerosis.

Sawcer S, Goodfellow PN.

Curr Opin Immunol. 1998 Dec;10(6):697-703. Review.

PMID:
9914228
19.

cDNA characterization and high resolution mapping of the human SOX20 gene.

Vujić M, Rajić T, Goodfellow PN, Stevanović M.

Mamm Genome. 1998 Dec;9(12):1059-61. No abstract available.

PMID:
9880678
20.

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain gene cluster.

Feakes R, Chataway J, Sawcer S, Jones HB, Clayton D, Goodfellow PN, Compston A.

Ann Neurol. 1998 Dec;44(6):984. No abstract available.

PMID:
9851448
21.

Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia.

Wunderle VM, Critcher R, Hastie N, Goodfellow PN, Schedl A.

Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10649-54.

22.

Molecular analysis of 9p deletions associated with XY sex reversal: refining the localization of a sex-determining gene to the tip of the chromosome.

Guioli S, Schmitt K, Critcher R, Bouzyk M, Spurr NK, Ogata T, Hoo JJ, Pinsky L, Gimelli G, Pasztor L, Goodfellow PN.

Am J Hum Genet. 1998 Sep;63(3):905-8. No abstract available.

23.

Characterization of whole genome radiation hybrid mapping resources for non-mammalian vertebrates.

Kwok C, Korn RM, Davis ME, Burt DW, Critcher R, McCarthy L, Paw BH, Zon LI, Goodfellow PN, Schmitt K.

Nucleic Acids Res. 1998 Aug 1;26(15):3562-6.

24.

A first-generation whole genome-radiation hybrid map spanning the mouse genome.

McCarthy LC, Terrett J, Davis ME, Knights CJ, Smith AL, Critcher R, Schmitt K, Hudson J, Spurr NK, Goodfellow PN.

Genome Res. 1997 Dec;7(12):1153-61.

25.

Integrated radiation hybrid and yeast artificial chromosome map of chromosome 9p.

Bouzyk M, Bryant SP, Evans C, Guioli S, Ford S, Schmidt K, Goodfellow PN, Povey S, Rebello M, Rousseaux S, Spurr NK.

Eur J Hum Genet. 1997 Sep-Oct;5(5):299-307.

PMID:
9412787
26.

Genetics of disease.

Goodfellow PN, Camerino G.

Curr Opin Genet Dev. 1997 Jun 1;7(3):329-30. No abstract available.

PMID:
9548965
27.

The genetic analysis of multiple sclerosis.

Sawcer S, Goodfellow PN, Compston A.

Trends Genet. 1997 Jun;13(6):234-9. Review.

PMID:
9196329
28.

SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene.

Lefebvre V, Huang W, Harley VR, Goodfellow PN, de Crombrugghe B.

Mol Cell Biol. 1997 Apr;17(4):2336-46.

29.

Empirical genomewide significance levels established by whole genome simulations.

Sawcer S, Jones HB, Judge D, Visser F, Compston A, Goodfellow PN, Clayton D.

Genet Epidemiol. 1997;14(3):223-9.

PMID:
9181352
30.

Sex determination in humans.

Schafer AJ, Goodfellow PN.

Bioessays. 1996 Dec;18(12):955-63. Review.

PMID:
8976152
31.

A gene map of the human genome.

Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tomé P, Aggarwal A, Bajorek E, Bentolila S, Birren BB, Butler A, Castle AB, Chiannilkulchai N, Chu A, Clee C, Cowles S, Day PJ, Dibling T, Drouot N, Dunham I, Duprat S, East C, Edwards C, Fan JB, Fang N, Fizames C, Garrett C, Green L, Hadley D, Harris M, Harrison P, Brady S, Hicks A, Holloway E, Hui L, Hussain S, Louis-Dit-Sully C, Ma J, MacGilvery A, Mader C, Maratukulam A, Matise TC, McKusick KB, Morissette J, Mungall A, Muselet D, Nusbaum HC, Page DC, Peck A, Perkins S, Piercy M, Qin F, Quackenbush J, Ranby S, Reif T, Rozen S, Sanders C, She X, Silva J, Slonim DK, Soderlund C, Sun WL, Tabar P, Thangarajah T, Vega-Czarny N, Vollrath D, Voyticky S, Wilmer T, Wu X, Adams MD, Auffray C, Walter NA, Brandon R, Dehejia A, Goodfellow PN, Houlgatte R, Hudson JR Jr, Ide SE, Iorio KR, Lee WY, Seki N, Nagase T, Ishikawa K, Nomura N, Phillips C, Polymeropoulos MH, Sandusky M, Schmitt K, Berry R, Swanson K, Torres R, Venter JC, Sikela JM, Beckmann JS, Weissenbach J, Myers RM, Cox DR, James MR, Bentley D, Deloukas P, Lander ES, Hudson TJ.

Science. 1996 Oct 25;274(5287):540-6. Review.

PMID:
8849440
32.

A radiation hybrid map spanning the entire human X chromosome integrating YACs, genes, and STS markers.

Kumlien J, Grigoriev A, Roest Crollius H, Ross M, Goodfellow PN, Lehrach H.

Mamm Genome. 1996 Oct;7(10):758-66.

PMID:
8854864
33.
34.

Cloning and characterization of SOX5, a new member of the human SOX gene family.

Wunderle VM, Critcher R, Ashworth A, Goodfellow PN.

Genomics. 1996 Sep 1;36(2):354-8.

PMID:
8812465
35.

The HMG box of SRY is a calmodulin binding domain.

Harley VR, Lovell-Badge R, Goodfellow PN, Hextall PJ.

FEBS Lett. 1996 Aug 5;391(1-2):24-8.

36.

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22.

Sawcer S, Jones HB, Feakes R, Gray J, Smaldon N, Chataway J, Robertson N, Clayton D, Goodfellow PN, Compston A.

Nat Genet. 1996 Aug;13(4):464-8.

PMID:
8696343
37.

Campomelic dysplasia with XY sex reversal: diverse phenotypes resulting from mutations in a single gene.

Schafer AJ, Foster JW, Kwok C, Weller PA, Guioli S, Goodfellow PN.

Ann N Y Acad Sci. 1996 Jun 8;785:137-49. Review. No abstract available.

PMID:
8702120
38.

Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects.

Kwok C, Tyler-Smith C, Mendonca BB, Hughes I, Berkovitz GD, Goodfellow PN, Hawkins JR.

J Med Genet. 1996 Jun;33(6):465-8.

39.

Regional assignment of human ESTs by whole-genome radiation hybrid mapping.

Hayes PD, Schmitt K, Jones HB, Gyapay G, Weissenbach J, Goodfellow PN.

Mamm Genome. 1996 Jun;7(6):446-50.

PMID:
8662228
40.

Construction of a mouse whole-genome radiation hybrid panel and application to MMU11.

Schmitt K, Foster JW, Feakes RW, Knights C, Davis ME, Spillett DJ, Goodfellow PN.

Genomics. 1996 Jun 1;34(2):193-7.

PMID:
8661048
41.

Construction of a radiation hybrid map of chromosome 9p.

Bouzyk M, Bryant SP, Schmitt K, Goodfellow PN, Ekong R, Spurr NK.

Genomics. 1996 Jun 1;34(2):187-92.

PMID:
8661047
42.

A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK.

Foster JW, Schafer AJ, Critcher R, Spillett DJ, Feakes RW, Walter MA, Dominguez-Steglich M, Guioli S, Brook JD, Goodfellow PN.

Genomics. 1996 Apr 15;33(2):185-92.

PMID:
8660966
43.

A radiation hybrid map of the human genome.

Gyapay G, Schmitt K, Fizames C, Jones H, Vega-Czarny N, Spillett D, Muselet D, Prud'homme JF, Dib C, Auffray C, Morissette J, Weissenbach J, Goodfellow PN.

Hum Mol Genet. 1996 Mar;5(3):339-46.

PMID:
8852657
44.

A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2.

Collignon J, Sockanathan S, Hacker A, Cohen-Tannoudji M, Norris D, Rastan S, Stevanovic M, Goodfellow PN, Lovell-Badge R.

Development. 1996 Feb;122(2):509-20.

45.

A high-resolution radiation hybrid map of the region surrounding the Gorlin syndrome gene.

Obermayr F, Walter MA, Jones HB, Goodfellow PN, Frischauf AM.

Eur J Hum Genet. 1996;4(4):242-5.

PMID:
8875192
46.

The role of SOX9 in autosomal sex reversal and campomelic dysplasia.

Schafer AJ, Dominguez-Steglich MA, Guioli S, Kwok C, Weller PA, Stevanovic M, Weissenbach J, Mansour S, Young ID, Goodfellow PN, et al.

Philos Trans R Soc Lond B Biol Sci. 1995 Nov 29;350(1333):271-7; discussion 277-8.

PMID:
8570691
47.

Interaction of normal and mutant SRY proteins with DNA.

Rimini R, Pontiggia A, Spada F, Ferrari S, Harley VR, Goodfellow PN, Bianchi ME.

Philos Trans R Soc Lond B Biol Sci. 1995 Nov 29;350(1333):215-20.

PMID:
8570684
48.

Sequence variation of the human Y chromosome.

Whitfield LS, Sulston JE, Goodfellow PN.

Nature. 1995 Nov 23;378(6555):379-80.

PMID:
7477372
49.

41 kilobases of analyzed sequence from the pseudoautosomal and sex-determining regions of the short arm of the human Y chromosome.

Whitfield LS, Hawkins TL, Goodfellow PN, Sulston J.

Genomics. 1995 May 20;27(2):306-11.

PMID:
7557997
50.

The human Y chromosome homologue of XG: transcription of a naturally truncated gene.

Weller PA, Critcher R, Goodfellow PN, German J, Ellis NA.

Hum Mol Genet. 1995 May;4(5):859-68.

PMID:
7633446

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