21 results for author:"Adams S.M." in Literature citations
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| Decorin expression is important for age-related changes in tendon structure and mechanical properties. Dunkman A.A., Buckley M.R., Mienaltowski M.J., Adams S.M., Thomas S.J., Satchell L., Kumar A., Pathmanathan L., Beason D.P., Iozzo R.V. et al. Matrix Biol. 32:3-13(2013) · Mapped (10) |
| High throughput mass spectrometry-based mutation profiling of primary uveal melanoma. Daniels A.B., Lee J.E., MacConaill L.E., Palescandolo E., Van Hummelen P., Adams S.M., DeAngelis M.M., Hahn W.C., Gragoudas E.S., Harbour J.W. et al. Invest. Ophthalmol. Vis. Sci. 53:6991-6996(2012) · Mapped (9) |
| Collagen V is a dominant regulator of collagen fibrillogenesis: dysfunctional regulation of structure and function in a corneal-stroma-specific Col5a1-null mouse model. Sun M., Chen S., Adams S.M., Florer J.B., Liu H., Kao W.W., Wenstrup R.J., Birk D.E. J. Cell. Sci. 124:4096-4105(2011) · Mapped (2) |
| Genome sequence of Streptomyces griseus strain XylebKG-1, an ambrosia beetle-associated actinomycete. Grubbs K.J., Biedermann P.H., Suen G., Adams S.M., Moeller J.A., Klassen J.L., Goodwin L.A., Woyke T., Munk A.C., Bruce D. et al. J. Bacteriol. 193:2890-2891(2011) · UniProtKB (7,193) |
| Prospective study of common variants in the retinoic acid receptor-related orphan receptor alpha gene and risk of neovascular age-related macular degeneration. Schaumberg D.A., Chasman D., Morrison M.A., Adams S.M., Guo Q., Hunter D.J., Hankinson S.E., DeAngelis M.M. Arch. Ophthalmol. 128:1462-1471(2010) · Mapped (3) |
| Peroxisome proliferator-activated receptor delta agonists inhibit T helper type 1 (Th1) and Th17 responses in experimental allergic encephalomyelitis. Kanakasabai S., Chearwae W., Walline C.C., Iams W., Adams S.M., Bright J.J. Immunology 130:572-588(2010) · Mapped (4) |
| Comprehensive analysis of complement factor H and LOC387715/ARMS2/HTRA1 variants with respect to phenotype in advanced age-related macular degeneration. Andreoli M.T., Morrison M.A., Kim B.J., Chen L., Adams S.M., Miller J.W., DeAngelis M.M., Kim I.K. Am. J. Ophthalmol. 148:869-874(2009) · Mapped (9) |
| Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: a systems biology based approach. Silveira A.C., Morrison M.A., Ji F., Xu H., Reinecke J.B., Adams S.M., Arneberg T.M., Janssian M., Lee J.E., Yuan Y. et al. Vision Res. 50:698-715(2010) · Mapped (3) |
| Stat4 isoforms differentially regulate inflammation and demyelination in experimental allergic encephalomyelitis. Mo C., Chearwae W., O'Malley J.T., Adams S.M., Kanakasabai S., Walline C.C., Stritesky G.L., Good S.R., Perumal N.B., Kaplan M.H. et al. J. Immunol. 181:5681-5690(2008) · Mapped (7) |
| Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y. Jobling M.A., Lo I.C., Turner D.J., Bowden G.R., Lee A.C., Xue Y., Carvalho-Silva D., Hurles M.E., Adams S.M., Chang Y.M. et al. Hum. Mol. Genet. 16:307-316(2007) · Mapped (1) |
| Teleost fish genomes contain a diverse array of L1 retrotransposon lineages that exhibit a low copy number and high rate of turnover. Duvernell D.D., Pryor S.R., Adams S.M. J. Mol. Evol. 59:298-308(2004) · UniProtKB (73) |
| Limited role of developmental programmed cell death pathways in Drosophila norpA retinal degeneration. Hsu C.D., Whaley M.A., Frazer K., Miller D.A., Mitchell K.A., Adams S.M., O'Tousa J.E. J. Neurosci. 24:500-507(2004) · Mapped (14) |
| An evolutionarily conserved N-terminal acetyltransferase complex associated with neuronal development. Sugiura N., Adams S.M., Corriveau R.A. J. Biol. Chem. 278:40113-40120(2003) · UniProtKB (3) · Mapped (16) |
| Rpr- and hid-driven cell death in Drosophila photoreceptors. Hsu C.D., Adams S.M., O'Tousa J.E. Vision Res. 42:507-516(2002) · Mapped (2) |
| Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1). Berson E.L., Grimsby J.L., Adams S.M., McGee T.L., Sweklo E., Pierce E.A., Sandberg M.A., Dryja T.P. Invest. Ophthalmol. Vis. Sci. 42:2217-2224(2001) · UniProtKB (1) |
| Null RPGRIP1 alleles in patients with Leber congenital amaurosis. Dryja T.P., Adams S.M., Grimsby J.L., McGee T.L., Hong D.H., Li T., Andreasson S., Berson E.L. Am. J. Hum. Genet. 68:1295-1298(2001) · Mapped (2) |
| The Drosophila melanogaster homologue of the human BBC1 gene is highly expressed during embryogenesis. Helps N.R., Adams S.M., Brammar W.J., Varley J.M. |
| A sequence previously identified as metastasis-related encodes an acidic ribosomal phosphoprotein, P2. Sharp M.G.F., Adams S.M., Elvin P., Walker R.A., Brammar W.J., Varley J.M. Br. J. Cancer 61:83-88(1990) · UniProtKB (1) |
| Genetic organization of the KpnI restriction-modification system. Chatterjee D.K., Hammond A.W., Blakesley R.W., Adams S.M., Gerard G.F. Nucleic Acids Res. 19:6505-6509(1991) · UniProtKB (2) |
| Differential expression of translation-associated genes in benign and malignant human breast tumours. Adams S.M., Sharp M.G., Walker R.A., Brammar W.J., Varley J.M. Br. J. Cancer 65:65-71(1992) · UniProtKB (1) |
| Isolation and characterization of a novel gene with differential expression in benign and malignant human breast tumours. Adams S.M., Helps N.R., Sharp M.G.F., Brammar W.J., Walker R.A., Varley J.M. Hum. Mol. Genet. 1:91-96(1992) · UniProtKB (1) |