5 results for author:"Dalgliesh G.L." in Literature citations
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| Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma. Varela I., Tarpey P., Raine K., Huang D., Ong C.K., Stephens P., Davies H., Jones D., Lin M.L., Teague J. et al. Nature 469:539-542(2011) · UniProtKB (74) |
| Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes. Dalgliesh G.L., Furge K., Greenman C., Chen L., Bignell G., Butler A., Davies H., Edkins S., Hardy C., Latimer C. et al. Nature 463:360-363(2010) · Mapped (20) |
| 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 (17) |
| 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) |
| Expansion of GAA triplet repeats in the human genome: unique origin of the FRDA mutation at the center of an Alu. Clark R.M., Dalgliesh G.L., Endres D., Gomez M., Taylor J., Bidichandani S.I. Genomics 83:373-383(2004) · Mapped (3) |