14
results
for author:"Dicks E."
in Literature Citations
| Pioglitazone induced gastric acid secretion. Rotte A., Mack A.F., Bhandaru M., Kempe D.S., Beier N., Scholz W., Dicks E., Potzsch S., Kuhl D., Lang F. Cell. Physiol. Biochem. 24:193-200(2009) · Mapped (2) |
| Family history of renal disease severity predicts the mutated gene in ADPKD. Barua M., Cil O., Paterson A.D., Wang K., He N., Dicks E., Parfrey P., Pei Y. J. Am. Soc. Nephrol. 20:1833-1838(2009) · Mapped (5) |
| X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. Dibbens L.M., Tarpey P.S., Hynes K., Bayly M.A., Scheffer I.E., Smith R., Bomar J., Sutton E., Vandeleur L., Shoubridge C. et al. |
| MSH2 118T>C and MSH6 159C>T promoter polymorphisms and the risk of colorectal cancer. Mrkonjic M., Raptis S., Green R.C., Monga N., Daftary D., Dicks E., Younghusband H.B., Parfrey P.S., Gallinger S.S., McLaughlin J.R. et al. Carcinogenesis 28:2575-2580(2007) · Mapped (19) |
| 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) |
| MLH1 -93G>A promoter polymorphism and the risk of microsatellite-unstable colorectal cancer. Raptis S., Mrkonjic M., Green R.C., Pethe V.V., Monga N., Chan Y.M., Daftary D., Dicks E., Younghusband B.H., Parfrey P.S. et al. J. Natl. Cancer Inst. 99:463-474(2007) · Mapped (30) |
| 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) |
| 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 (2) |
| 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) |
| 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) |
| Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease. Magistroni R., He N., Wang K., Andrew R., Johnson A., Gabow P., Dicks E., Parfrey P., Torra R., San-Millan J.L. et al. J. Am. Soc. Nephrol. 14:1164-1174(2003) · 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. |
