12 results for author:"Teh M.T." in Literature citations
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| FOXM1 induces a global methylation signature that mimics the cancer epigenome in head and neck squamous cell carcinoma. Teh M.T., Gemenetzidis E., Patel D., Tariq R., Nadir A., Bahta A.W., Waseem A., Hutchison I.L. PLoS ONE 7:e34329-e34329(2012) · Mapped (3) |
| Desmoglein 3, via an interaction with E-cadherin, is associated with activation of Src. Tsang S.M., Liu L., Teh M.T., Wheeler A., Grose R., Hart I.R., Garrod D.R., Fortune F., Wan H. PLoS ONE 5:e14211-e14211(2010) · Mapped (11) |
| Induction of human epithelial stem/progenitor expansion by FOXM1. Gemenetzidis E., Elena-Costea D., Parkinson E.K., Waseem A., Wan H., Teh M.T. Cancer Res. 70:9515-9526(2010) · Mapped (3) |
| A molecular study of desmosomes identifies a desmoglein isoform switch in head and neck squamous cell carcinoma. Teh M.T., Parkinson E.K., Thurlow J.K., Liu F., Fortune F., Wan H. J. Oral Pathol. Med. 40:67-76(2011) · Mapped (3) |
| Downstream targets of FOXM1: CEP55 and HELLS are cancer progression markers of head and neck squamous cell carcinoma. Waseem A., Ali M., Odell E.W., Fortune F., Teh M.T. Oral Oncol. 46:536-542(2010) · Mapped (10) |
| EPS8 upregulates FOXM1 expression, enhancing cell growth and motility. Wang H., Teh M.T., Ji Y., Patel V., Firouzabadian S., Patel A.A., Gutkind J.S., Yeudall W.A. Carcinogenesis 31:1132-1141(2010) · Mapped (5) |
| Upregulation of FOXM1 induces genomic instability in human epidermal keratinocytes. Teh M.T., Gemenetzidis E., Chaplin T., Young B.D., Philpott M.P. Mol. Cancer 9:45-45(2010) · Mapped (3) |
| Upregulation of HIF-1alpha in malignant transformation of oral submucous fibrosis. Tilakaratne W.M., Iqbal Z., Teh M.T., Ariyawardana A., Pitiyage G., Cruchley A., Stewart J.E., Hagi-Pavli E., Lalli A., Waseem A. et al. J. Oral Pathol. Med. 37:372-377(2008) · Mapped (9) |
| Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis. Purdie K.J., Lambert S.R., Teh M.T., Chaplin T., Molloy G., Raghavan M., Kelsell D.P., Leigh I.M., Harwood C.A., Proby C.M. et al. Genes Chromosomes Cancer 46:661-669(2007) · Mapped (8) |
| Role for WNT16B in human epidermal keratinocyte proliferation and differentiation. Teh M.T., Blaydon D., Ghali L.R., Briggs V., Edmunds S., Pantazi E., Barnes M.R., Leigh I.M., Kelsell D.P., Philpott M.P. J. Cell. Sci. 120:330-339(2007) |
| The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia. Blaydon D.C., Ishii Y., O'Toole E.A., Unsworth H.C., Teh M.-T., Rueschendorf F., Sinclair C., Hopsu-Havu V.K., Tidman N., Moss C. et al. |
| Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. Kelsell D.P., Norgett E.E., Unsworth H., Teh M.-T., Cullup T., Mein C.A., Dopping-Hepenstal P.J., Dale B.A., Tadini G., Fleckman P. et al. Am. J. Hum. Genet. 76:794-803(2005) · UniProtKB (1) · Mapped (1) |