11
results
for author:"Boright A.P."
in Literature Citations
| Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. Paterson A.D., Lopes-Virella M.F., Waggott D., Boright A.P., Hosseini S.M., Carter R.E., Shen E., Mirea L., Bharaj B., Sun L. et al. Arterioscler. Thromb. Vasc. Biol. 29:1958-1967(2009) · Mapped (118) |
| Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes. Pezzolesi M.G., Poznik G.D., Mychaleckyj J.C., Paterson A.D., Barati M.T., Klein J.B., Ng D.P., Placha G., Canani L.H., Bochenski J. et al. Diabetes 58:1403-1410(2009) · Mapped (10) |
| Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study. Al-Kateb H., Boright A.P., Mirea L., Xie X., Sutradhar R., Mowjoodi A., Bharaj B., Liu M., Bucksa J.M., Arends V.L. et al. Diabetes 57:218-228(2008) · Mapped (3) |
| Multiple variants in vascular endothelial growth factor (VEGFA) are risk factors for time to severe retinopathy in type 1 diabetes: the DCCT/EDIC genetics study. Al-Kateb H., Mirea L., Xie X., Sun L., Liu M., Chen H., Bull S.B., Boright A.P., Paterson A.D. Diabetes 56:2161-2168(2007) · Mapped (7) |
| LDL composition in E2/2 subjects and LDL distribution by Apo E genotype in type 1 diabetes. Murdoch S.J., Boright A.P., Paterson A.D., Zinman B., Steffes M., Cleary P., Edwards K., Marcovina S.S., Purnell J.Q., Brunzell J.D. Atherosclerosis 192:138-147(2007) · Mapped (6) |
| Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics Study. Boright A.P., Paterson A.D., Mirea L., Bull S.B., Mowjoodi A., Scherer S.W., Zinman B. Diabetes 54:1238-1244(2005) · Mapped (7) |
| Human chromosome 7: DNA sequence and biology. Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R. et al. Science 300:767-772(2003) · UniProtKB (658) |
| Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome. Petek E., Windpassinger C., Vincent J.B., Cheung J., Boright A.P., Scherer S.W., Kroisel P.M., Wagner K. Am. J. Hum. Genet. 68:848-858(2001) · UniProtKB (2) |
| Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5. Wilson M.D., Riemer C., Martindale D.W., Schnupf P., Boright A.P., Cheung T.L., Hardy D.M., Schwartz S., Scherer S.W., Tsui L.-C. et al. Nucleic Acids Res. 29:1352-1365(2001) · UniProtKB (20) · Mapped (17) |
| The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. Kobayashi K., Sinasac D.S., Iijima M., Boright A.P., Begum L., Lee J.R., Yasuda T., Ikeda S., Hirano R., Terazono H. et al. Nat. Genet. 22:159-163(1999) · UniProtKB (2) |
| Large-scale sequencing of two regions in human chromosome 7q22: analysis of 650 kb of genomic sequence around the EPO and CUTL1 loci reveals 17 genes. Gloeckner G., Scherer S., Schattevoy R., Boright A.P., Weber J., Tsui L.-C., Rosenthal A. Genome Res. 8:1060-1073(1998) · UniProtKB (11) |
