13 results for author:"Barnes M.R." in Literature citations
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| A COMT gene haplotype associated with methamphetamine abuse. Jugurnauth S.K., Chen C.K., Barnes M.R., Li T., Lin S.K., Liu H.C., Collier D.A., Breen G. Pharmacogenet. Genomics 21:731-740(2011) · Mapped (7) |
| ADAMTSL3 as a candidate gene for schizophrenia: gene sequencing and ultra-high density association analysis by imputation. Dow D.J., Huxley-Jones J., Hall J.M., Francks C., Maycox P.R., Kew J.N., Gloger I.S., Mehta N.A., Kelly F.M., Muglia P. et al. Schizophr. Res. 127:28-34(2011) · Mapped (1) |
| Genome-wide association study of major recurrent depression in the U.K. population. Lewis C.M., Ng M.Y., Butler A.W., Cohen-Woods S., Uher R., Pirlo K., Weale M.E., Schosser A., Paredes U.M., Rivera M. et al. Am J Psychiatry 167:949-957(2010) · Mapped (3) |
| Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. Uher R., Perroud N., Ng M.Y., Hauser J., Henigsberg N., Maier W., Mors O., Placentino A., Rietschel M., Souery D. et al. Am J Psychiatry 167:555-564(2010) · Mapped (5) |
| Disruption of the neurexin 1 gene is associated with schizophrenia. Rujescu D., Ingason A., Cichon S., Pietilainen O.P., Barnes M.R., Toulopoulou T., Picchioni M., Vassos E., Ettinger U., Bramon E. et al. Hum. Mol. Genet. 18:988-996(2009) · Mapped (8) |
| Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. Li H., Wetten S., Li L., St Jean P.L., Upmanyu R., Surh L., Hosford D., Barnes M.R., Briley J.D., Borrie M. et al. Arch. Neurol. 65:45-53(2008) · Mapped (14) |
| Polymorphisms in the endothelin-1 (EDN1) are associated with asthma in two populations. Zhu G., Carlsen K., Carlsen K.H., Lenney W., Silverman M., Whyte M.K., Hosking L., Helms P., Roses A.D., Hay D.W. et al. Genes Immun. 9:23-29(2008) · Mapped (2) |
| 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) |
| Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland. McGinnis R.E., Fox H., Yates P., Cameron L.A., Barnes M.R., Gray I.C., Spurr N.K., Hurko O., St Clair D. Nat. Genet. 28:128-129(2001) · Mapped (6) |
| Wnt-16a, a novel Wnt-16 isoform, which shows differential expression in adult human tissues. Fear M.W., Kelsell D.P., Spurr N.K., Barnes M.R. Biochem. Biophys. Res. Commun. 278:814-820(2000) · UniProtKB (1) |
| Cloning and characterisation of ITGAV, the genomic sequence for human cell adhesion protein (vitronectin) receptor alpha subunit, CD51. Sims M.A., Field S., Barnes M.R., Shaikh N., Ellington K., Murphy K.E., Spurr N.K., Campbell D.A. Cytogenet. Cell Genet. 89:268-271(2000) · UniProtKB (1) · Mapped (7) |
| Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis. Wilgoss A., Leigh I.M., Barnes M.R., Dopping-Hepenstal P., Eady R.A.J., Walter J.M., Kennedy C.T., Kelsell D.P. J. Invest. Dermatol. 113:1119-1122(1999) · UniProtKB (1) |
| A 3-(3-hydroxyphenyl)propionic acid catabolic pathway in Rhodococcus globerulus PWD1: cloning and characterization of the hpp operon. Barnes M.R., Duetz W.A., Williams P.A. J. Bacteriol. 179:6145-6153(1997) · UniProtKB (5) |