15
results
for author:"Bignell G."
in Literature Citations
| Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer. van Haaften G., Dalgliesh G.L., Davies H., Chen L., Bignell G., Greenman C., Edkins S., Hardy C., O'Meara S., Teague J. et al. Nat. Genet. 41:521-523(2009) · Mapped (12) |
| Feedback circuit among INK4 tumor suppressors constrains human glioblastoma development. Wiedemeyer R., Brennan C., Heffernan T.P., Xiao Y., Mahoney J., Protopopov A., Zheng H., Bignell G., Furnari F., Cavenee W.K. et al. Cancer Cell 13:355-364(2008) · Mapped (10) |
| 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) |
| 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) |
| Lung cancer: intragenic ERBB2 kinase mutations in tumours. Stephens P., Hunter C., Bignell G., Edkins S., Davies H., Teague J., Stevens C., O'Meara S., Smith R., Parker A. et al. Nature 431:525-526(2004) · Mapped (8) |
| 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 (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. |
| Identification of the familial cylindromatosis tumor suppressor gene. Bignell G.R., Brown C., Biggs P.J., Lakhani S.R., Jones C., Hansen J., Blair E., Hofmann B., Siebert R., Turner G. et al. Nat. Genet. 25:160-165(2000) · UniProtKB (1) |
| Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer. Bignell G.R., Barfoot R., Seal S., Collins N., Warren W., Stratton M.R. Cancer Res. 58:1384-1386(1998) · UniProtKB (1) |
| A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Hemminki A., Markie D., Tomlinson I., Avizienyte E., Roth S., Loukola A., Bignell G., Warren W., Aminoff M., Hoeglund P. et al. |
| 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) |
| Electrophoretic karyotype of the amylolytic yeast Lipomyces starkeyi and cloning, sequencing and chromosomal localization of its TRP1 gene. Bignell G.R., Bruce I.J., Evans I.H. |
| 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) |
| Identification of the breast cancer susceptibility gene BRCA2. Wooster R., Bignell G., Lancaster J., Swift S., Seal S., Mangion J., Collins N., Gregory S., Gumbs C., Micklem G. et al. Nature 378:789-792(1995) · UniProtKB (1) |
| Isolation of a DNA fragment which complements glutamine synthetase deficient strains of S. pombe. Barel I., Bignell G., Simpson A., MacDonald D. Curr. Genet. 13:487-494(1988) · UniProtKB (1) |
