1 - 25 of 29 results for author:"Wooster R." in Literature citations
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| Comprehensive predictive biomarker analysis for MEK inhibitor GSK1120212. Jing J., Greshock J., Holbrook J.D., Gilmartin A., Zhang X., McNeil E., Conway T., Moy C., Laquerre S., Bachman K. et al. Mol. Cancer Ther. 11:720-729(2012) · Mapped (4) |
| Sensitivity of cancer cells to Plk1 inhibitor GSK461364A is associated with loss of p53 function and chromosome instability. Degenhardt Y., Greshock J., Laquerre S., Gilmartin A.G., Jing J., Richter M., Zhang X., Bleam M., Halsey W., Hughes A. et al. Mol. Cancer Ther. 9:2079-2089(2010) · Mapped (32) |
| Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases. Qian F., Engst S., Yamaguchi K., Yu P., Won K.A., Mock L., Lou T., Tan J., Li C., Tam D. et al. Cancer Res. 69:8009-8016(2009) · Mapped (1) |
| A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. Tarpey P.S., Smith R., Pleasance E., Whibley A., Edkins S., Hardy C., O'Meara S., Latimer C., Dicks E., Menzies A. et al. |
| Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. Tarpey P.S., Raymond F.L., Nguyen L.S., Rodriguez J., Hackett A., Vandeleur L., Smith R., Shoubridge C., Edkins S., Stevens C. et al. |
| Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly. Field M., Tarpey P.S., Smith R., Edkins S., O'Meara S., Stevens C., Tofts C., Teague J., Butler A., Dicks E. et al. Am. J. Hum. Genet. 81:367-374(2007) · UniProtKB (1) |
| Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus. Raymond F.L., Tarpey P.S., Edkins S., Tofts C., O'Meara S., Teague J., Butler A., Stevens C., Barthorpe S., Buck G. et al. Am. J. Hum. Genet. 80:982-987(2007) · UniProtKB (1) |
| Patterns of somatic mutation in human cancer genomes. Greenman C., Stephens P., Smith R., Dalgliesh G.L., Hunter C., Bignell G., Davies H., Teague J., Butler A., Stevens C. et al. Nature 446:153-158(2007) · UniProtKB (453) |
| A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia. Tarpey P., Pemberton T.J., Stockton D.W., Das P., Ninis V., Edkins S., Andrew Futreal P., Wooster R., Kamath S., Nayak R. et al. Am. J. Med. Genet. A 143:390-394(2007) · UniProtKB (1) |
| Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor. Tarpey P.S., Raymond F.L., O'Meara S., Edkins S., Teague J., Butler A., Dicks E., Stevens C., Tofts C., Avis T. et al. Am. J. Hum. Genet. 80:345-352(2007) · UniProtKB (1) · Mapped (1) |
| Mutations in the gene encoding the sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation. Tarpey P.S., Stevens C., Teague J., Edkins S., O'Meara S., Avis T., Barthorpe S., Buck G., Butler A., Cole J. et al. Am. J. Hum. Genet. 79:1119-1124(2006) · UniProtKB (1) |
| Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation. Field M., Tarpey P., Boyle J., Edkins S., Goodship J., Luo Y., Moon J., Teague J., Stratton M.R., Futreal P.A. et al. |
| Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus. Tarpey P., Thomas S., Sarvananthan N., Mallya U., Lisgo S., Talbot C.J., Roberts E.O., Awan M., Surendran M., McLean R.J. et al. Nat. Genet. 38:1242-1244(2006) · UniProtKB (1) |
| The DNA sequence and biological annotation of human chromosome 1. Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A. et al. Nature 441:315-321(2006) · UniProtKB (5,143) |
| The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders. Scott L.M., Campbell P.J., Baxter E.J., Todd T., Stephens P., Edkins S., Wooster R., Stratton M.R., Futreal P.A., Green A.R. Blood 106:2920-2921(2005) · Mapped (6) |
| Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults. Bignell G., Smith R., Hunter C., Stephens P., Davies H., Greenman C., Teague J., Butler A., Edkins S., Stevens C. et al. Genes Chromosomes Cancer 45:42-46(2006) · UniProtKB (2) |
| Somatic mutations of the protein kinase gene family in human lung cancer. Davies H., Hunter C., Smith R., Stephens P., Greenman C., Bignell G., Teague J., Butler A., Edkins S., Stevens C. et al. Cancer Res. 65:7591-7595(2005) · UniProtKB (1) |
| Lung cancer: intragenic ERBB2 kinase mutations in tumours. Cancer genome project and collaborative group |
| Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation. Tarpey P., Parnau J., Blow M., Woffendin H., Bignell G., Cox C., Cox J., Davies H., Edkins S., Holden S. et al. Am. J. Hum. Genet. 75:318-324(2004) · UniProtKB (1) · Mapped (5) |
| Amplification and overexpression of E2F3 in human bladder cancer. Feber A., Clark J., Goodwin G., Dodson A.R., Smith P.H., Fletcher A., Edwards S., Flohr P., Falconer A., Roe T. et al. Oncogene 23:1627-1630(2004) · Mapped (4) |
| Mutations of the BRAF gene in human cancer. Davies H., Bignell G.R., Cox C., Stephens P., Edkins S., Clegg S., Teague J., Woffendin H., Garnett M.J., Bottomley W. et al. |
| Screening for ESR mutations in breast and ovarian cancer patients. Anderson T.I., Wooster R., Laake K., Collins N., Warren W., Skrede M., Eeles R., Tveit K.M., Johnston S.R.D., Dowsett M. et al. Hum. Mutat. 9:531-536(1997) · UniProtKB (1) |
| Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene. Connor F., Smith A., Wooster R., Stratton M., Dixon A., Campbell E., Tait T.M., Freeman T., Ashworth A. Hum. Mol. Genet. 6:291-300(1997) · UniProtKB (1) · Mapped (25) |
| The BRC repeats are conserved in mammalian BRCA2 proteins. Bignell G., Micklem G., Stratton M.R., Ashworth A., Wooster R. Hum. Mol. Genet. 6:53-58(1997) · Mapped (3) |
| BRCA2 mutations in primary breast and ovarian cancers. Lancaster J.M., Wooster R., Mangion J., Phelan C.M., Cochran C., Gumbs C., Seal S., Barfoot R., Collins N., Bignell G. et al. Nat. Genet. 13:238-240(1996) · UniProtKB (1) |