13
results
for author:"Mungall A.J."
in Literature Citations
| Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians. SAVOIR Consortium Nat. Genet. 40:971-976(2008) · Mapped (2) |
| 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) |
| 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) |
| 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) |
| Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss. Schoenberger J., Wang L., Shin J.T., Kim S.D., Depreux F.F.S., Zhu H., Zon L., Pizard A., Kim J.B., Macrae C.A. et al. |
| 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 (1,563) |
| 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) |
| 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. |
| 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) |
| Vanin genes are clustered (human 6q22-24 and mouse 10A2B1) and encode isoforms of pantetheinase ectoenzymes. Martin F., Malergue F., Pitari G., Philippe J.M., Philips S., Chabret C., Granjeaud S., Mattei M.G., Mungall A.J., Naquet P. et al. Immunogenetics 53:296-306(2001) · Mapped (4) |
| Cloning and characterization of two overlapping genes in a subregion at 6q21 involved in replicative senescence and schizophrenia. Morelli C., Magnanini C., Mungall A.J., Negrini M., Barbanti-Brodano G. Gene 252:217-225(2000) · UniProtKB (1) |
| Alternative splicing, genomic structure, and fine chromosome localization of REV3L. Morelli C., Mungall A.J., Negrini M., Barbanti-Brodano G., Croce C.M. Cytogenet. Cell Genet. 83:18-20(1998) · UniProtKB (1) · 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) |
