1 - 25 of
35
results
for author:"Dunham I."
in Literature Citations
| DNA methylation-histone modification relationships across the desmin locus in human primary cells. Lindahl Allen M., Koch C.M., Clelland G.K., Dunham I., Antoniou M. BMC Mol. Biol. 10:51-51(2009) · Mapped (16) |
| Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level. Bruce A.W., Lopez-Contreras A.J., Flicek P., Down T.A., Dhami P., Dillon S.C., Koch C.M., Langford C.F., Dunham I., Andrews R.M. et al. Genome Res. 19:994-1005(2009) · Mapped (4) |
| Novel genes in cell cycle control and lipid metabolism with dynamically regulated binding sites for sterol regulatory element-binding protein 1 and RNA polymerase II in HepG2 cells detected by chromatin immunoprecipitation with microarray detection. Motallebipour M., Enroth S., Punga T., Ameur A., Koch C., Dunham I., Komorowski J., Ericsson J., Wadelius C. FEBS J. 276:1878-1890(2009) · Mapped (27) |
| Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians. SAVOIR Consortium Nat. Genet. 40:971-976(2008) · Mapped (3) |
| The evolution of the DLK1-DIO3 imprinted domain in mammals. Edwards C.A., Mungall A.J., Matthews L., Ryder E., Gray D.J., Pask A.J., Shaw G., Graves J.A., Rogers J., Dunham I. et al. PLoS Biol. 6:e135-e135(2008) · UniProtKB (4) |
| Tissue-specific histone modification and transcription factor binding in alpha globin gene expression. De Gobbi M., Anguita E., Hughes J., Sloane-Stanley J.A., Sharpe J.A., Koch C.M., Dunham I., Gibbons R.J., Wood W.G., Higgs D.R. Blood 110:4503-4510(2007) · Mapped (2) |
| Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11. Nejentsev S., Smink L.J., Smyth D., Bailey R., Lowe C.E., Payne F., Masters J., Godfrey L., Lam A., Burren O. et al. BMC Genet. 8:24-24(2007) · Mapped (3) |
| RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer. Bignone P.A., Lee K.Y., Liu Y., Emilion G., Finch J., Soosay A.E., Charnock F.M., Beck S., Dunham I., Mungall A.J. et al. Oncogene 26:683-700(2007) · Mapped (4) |
| 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 (2,571) |
| Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH. Ichimura K., Mungall A.J., Fiegler H., Pearson D.M., Dunham I., Carter N.P., Collins V.P. Oncogene 25:1261-1271(2006) · UniProtKB (1) |
| A genome annotation-driven approach to cloning the human ORFeome. Collins J.E., Wright C.L., Edwards C.A., Davis M.P., Grinham J.A., Cole C.G., Goward M.E., Aguado B., Mallya M., Mokrab Y. et al. Genome Biol. 5:R84.1-R84.11(2004) · UniProtKB (251) |
| DNA sequence and analysis of human chromosome 9. Humphray S.J., Oliver K., Hunt A.R., Plumb R.W., Loveland J.E., Howe K.L., Andrews T.D., Searle S., Hunt S.E., Scott C.E. et al. Nature 429:369-374(2004) · UniProtKB (1,091) |
| The DNA sequence and analysis of human chromosome 13. Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S. et al. Nature 428:522-528(2004) · UniProtKB (460) |
| The DNA sequence and analysis of human chromosome 6. Mungall A.J., Palmer S.A., Sims S.K., Edwards C.A., Ashurst J.L., Wilming L., Jones M.C., Horton R., Hunt S.E., Scott C.E. et al. Nature 425:805-811(2003) · UniProtKB (1,570) |
| beta-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation. Jeffries A.R., Mungall A.J., Dawson E., Halls K., Langford C.F., Murray R.M., Dunham I., Powell J.F. Mol. Psychiatry 8:654-663(2003) · Mapped (3) |
| Reevaluating human gene annotation: a second-generation analysis of chromosome 22. Collins J.E., Goward M.E., Cole C.G., Smink L.J., Huckle E.J., Knowles S., Bye J.M., Beare D.M., Dunham I. Genome Res. 13:27-36(2003) · UniProtKB (39) |
| The human homologue of unc-93 maps to chromosome 6q27 - characterisation and analysis in sporadic epithelial ovarian cancer. Liu Y., Dodds P., Emilion G., Mungall A.J., Dunham I., Beck S., Wells R.S., Charnock F.M.L., Ganesan T.S. |
| An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22. Jarmuz A., Chester A., Bayliss J., Gisbourne J., Dunham I., Scott J., Navaratnam N. Genomics 79:285-296(2002) · UniProtKB (6) |
| Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer. Liu Y., Emilion G., Mungall A.J., Dunham I., Beck S., LeMeuth-Metzinger V., Shelling A.N., Charnock F.M., Ganesan T.S. Oncogene 21:387-399(2002) · UniProtKB (2) |
| The DNA sequence of human chromosome 22. Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M., Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K. et al. |
| Psoriasis upregulated phorbolin-1 shares structural but not functional similarity to the mRNA-editing protein apobec-1. Madsen P.P., Anant S., Rasmussen H.H., Gromov P., Vorum H., Dumanski J.P., Tommerup N., Collins J.E., Wright C.L., Dunham I. et al. J. Invest. Dermatol. 113:162-169(1999) · UniProtKB (2) |
| Mapping and complex expression pattern of the human NPAP60L nucleoporin gene. Trichet V., Shkolny D., Dunham I., Beare D., McDermid H.E. Cytogenet. Cell Genet. 85:221-226(1999) · UniProtKB (1) |
| Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human. Southard-Smith E.M., Collins J.E., Ellison J.S., Smith K.J., Baxevanis A.D., Touchman J.W., Green E.D., Dunham I., Pavan W.J. Mamm. Genome 10:744-749(1999) · Mapped (42) |
| The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family. Peyrard M., Seroussi E., Sandberg-Nordqvist A.-C., Xie Y.-G., Han F.-Y., Fransson I., Collins J.E., Dunham I., Kost-Alimova M., Imreh S. et al. Proc. Natl. Acad. Sci. U.S.A. 96:598-603(1999) · UniProtKB (2) · Mapped (1) |
| Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Minassian B.A., Lee J.R., Herbrick J.-A., Huizenga J., Soder S., Mungall A.J., Dunham I., Gardner R., Fong C.G., Carpenter S. et al. Nat. Genet. 20:171-174(1998) · UniProtKB (1) |
