1 - 25 of 60 results for author:"Myers R.M." in Literature citations
Results Customize
› Repeat search in UniProtKB (37,407)
| A validated regulatory network for Th17 cell specification. Ciofani M., Madar A., Galan C., Sellars M., Mace K., Pauli F., Agarwal A., Huang W., Parkurst C.N., Muratet M. et al. |
| The hypersensitive glucocorticoid response specifically regulates period 1 and expression of circadian genes. Reddy T.E., Gertz J., Crawford G.E., Garabedian M.J., Myers R.M. Mol. Cell. Biol. 32:3756-3767(2012) · Mapped (14) |
| Gene expression changes in the prefrontal cortex, anterior cingulate cortex and nucleus accumbens of mood disorders subjects that committed suicide. Sequeira A., Morgan L., Walsh D.M., Cartagena P.M., Choudary P., Li J., Schatzberg A.F., Watson S.J., Akil H., Myers R.M. et al. PLoS ONE 7:e35367-e35367(2012) · Mapped (2) |
| Role of CCCTC binding factor (CTCF) and cohesin in the generation of single-cell diversity of protocadherin-alpha gene expression. Monahan K., Rudnick N.D., Kehayova P.D., Pauli F., Newberry K.M., Myers R.M., Maniatis T. Proc. Natl. Acad. Sci. U.S.A. 109:9125-9130(2012) · Mapped (11) |
| Dynamic microRNA gene transcription and processing during T cell development. Kirigin F.F., Lindstedt K., Sellars M., Ciofani M., Low S.L., Jones L., Bell F., Pauli F., Bonneau R., Myers R.M. et al. J. Immunol. 188:3257-3267(2012) · Mapped (16) |
| IkappaB kinase epsilon (IKK(epsilon)) regulates the balance between type I and type II interferon responses. Ng S.L., Friedman B.A., Schmid S., Gertz J., Myers R.M., Tenoever B.R., Maniatis T. Proc. Natl. Acad. Sci. U.S.A. 108:21170-21175(2011) · Mapped (6) |
| Research resource: enhanced genome-wide occupancy of estrogen receptor alpha by the cochaperone p23 in breast cancer cells. Simpson N.E., Gertz J., Imberg K., Myers R.M., Garabedian M.J. Mol. Endocrinol. 26:194-202(2012) · Mapped (6) |
| Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Psychiatric GWAS Consortium Bipolar Disorder Working Group Nat. Genet. 43:977-983(2011) · Mapped (16) |
| Lack of association to a NRG1 missense polymorphism in schizophrenia or bipolar disorder in a Costa Rican population. Moon E., Rollins B., Mesen A., Sequeira A., Myers R.M., Akil H., Watson S.J., Barchas J., Jones E.G., Schatzberg A. et al. Schizophr. Res. 131:52-57(2011) · Mapped (30) |
| Association of DRD2 and DRD3 polymorphisms with Parkinson's disease in a multiethnic consortium. McGuire V., Van Den Eeden S.K., Tanner C.M., Kamel F., Umbach D.M., Marder K., Mayeux R., Ritz B., Ross G.W., Petrovitch H. et al. J. Neurol. Sci. 307:22-29(2011) · Mapped (4) |
| DNA methylation profiling reveals novel biomarkers and important roles for DNA methyltransferases in prostate cancer. Kobayashi Y., Absher D.M., Gulzar Z.G., Young S.R., McKenney J.K., Peehl D.M., Brooks J.D., Myers R.M., Sherlock G. Genome Res. 21:1017-1027(2011) · Mapped (7) |
| A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia. Mendoza-Fandino G.A., Gee J.M., Ben-Dor S., Gonzalez-Quevedo C., Lee K., Kobayashi Y., Hartiala J., Myers R.M., Leal S.M., Allayee H. et al. Clin. Genet. 80:265-272(2011) · Mapped (6) |
| Allosteric modulation of hormone release from thyroxine and corticosteroid-binding globulins. Qi X., Loiseau F., Chan W.L., Yan Y., Wei Z., Milroy L.G., Myers R.M., Ley S.V., Read R.J., Carrell R.W. et al. J. Biol. Chem. 286:16163-16173(2011) · Mapped (4) |
| Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson's disease. Popat R.A., Van Den Eeden S.K., Tanner C.M., Kamel F., Umbach D.M., Marder K., Mayeux R., Ritz B., Ross G.W., Petrovitch H. et al. Eur. J. Neurol. 18:756-765(2011) · Mapped (6) |
| Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. Myocardial Infarction Genetics Consortium J. Am. Coll. Cardiol. 56:1552-1563(2010) · Mapped (6) |
| Complete HOX cluster characterization of the coelacanth provides further evidence for slow evolution of its genome. Amemiya C.T., Powers T.P., Prohaska S.J., Grimwood J., Schmutz J., Dickson M., Miyake T., Schoenborn M.A., Myers R.M., Ruddle F.H. et al. Proc. Natl. Acad. Sci. U.S.A. 107:3622-3627(2010) · UniProtKB (45) |
| Adaptive evolution of pelvic reduction in sticklebacks by recurrent deletion of a Pitx1 enhancer. Chan Y.F., Marks M.E., Jones F.C., Villarreal G. Jr., Shapiro M.D., Brady S.D., Southwick A.M., Absher D.M., Grimwood J., Schmutz J. et al. Science 327:302-305(2010) · UniProtKB (2) |
| Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging. Wheeler H.E., Metter E.J., Tanaka T., Absher D., Higgins J., Zahn J.M., Wilhelmy J., Davis R.W., Singleton A., Myers R.M. et al. PLoS Genet. 5:e1000685-e1000685(2009) · Mapped (343) |
| Genomic determination of the glucocorticoid response reveals unexpected mechanisms of gene regulation. Reddy T.E., Pauli F., Sprouse R.O., Neff N.F., Newberry K.M., Garabedian M.J., Myers R.M. Genome Res. 19:2163-2171(2009) · Mapped (12) |
| Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. Scott L.J., Muglia P., Kong X.Q., Guan W., Flickinger M., Upmanyu R., Tozzi F., Li J.Z., Burmeister M., Absher D. et al. Proc. Natl. Acad. Sci. U.S.A. 106:7501-7506(2009) · Mapped (20) |
| Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder. Rollins B., Martin M.V., Sequeira P.A., Moon E.A., Morgan L.Z., Watson S.J., Schatzberg A., Akil H., Myers R.M., Jones E.G. et al. PLoS ONE 4:e4913-e4913(2009) · Mapped (4) |
| Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. McGowan K.A., Li J.Z., Park C.Y., Beaudry V., Tabor H.K., Sabnis A.J., Zhang W., Fuchs H., de Angelis M.H., Myers R.M. et al. Nat. Genet. 40:963-970(2008) · Mapped (19) |
| Multiple transcription start sites for FOXP2 with varying cellular specificities. Schroeder D.I., Myers R.M. Gene 413:42-48(2008) · Mapped (9) |
| Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction. Knowles J.W., Wang H., Itakura H., Southwick A., Myers R.M., Iribarren C., Fortmann S.P., Go A.S., Quertermous T., Hlatky M.A. Am. Heart J. 154:1052-1058(2007) · Mapped (26) |
| Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease. Hlatky M.A., Ashley E., Quertermous T., Boothroyd D.B., Ridker P., Southwick A., Myers R.M., Iribarren C., Fortmann S.P., Go A.S. Am. Heart J. 154:1043-1051(2007) · Mapped (23) |