14
results
for author:"Palmer N."
in Literature Citations
| Association of SSTR2 polymorphisms and glucose homeostasis phenotypes: the Insulin Resistance Atherosclerosis Family Study. Sutton B.S., Palmer N.D., Langefeld C.D., Xue B., Proctor A., Ziegler J.T., Haffner S.M., Norris J.M., Bowden D.W. Diabetes 58:1457-1462(2009) · Mapped (2) |
| Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N. Tsui I., Chou C.L., Palmer N., Lin C.S., Tsang S.H. Curr. Eye Res. 33:1014-1022(2008) · Mapped (1) |
| Comprehensive dissection of PDGF-PDGFR signaling pathways in PDGFR genetically defined cells. Wu E., Palmer N., Tian Z., Moseman A.P., Galdzicki M., Wang X., Berger B., Zhang H., Kohane I.S. PLoS ONE 3:e3794-e3794(2008) · Mapped (5) |
| Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans. Palmer N.D., Langefeld C.D., Bryer-Ash M., Rotter J.I., Taylor K.D., Bowden D.W. J. Clin. Endocrinol. Metab. 93:4979-4983(2008) · Mapped (7) |
| Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1. Bento J.L., Palmer N.D., Zhong M., Roh B., Lewis J.P., Wing M.R., Pandya H., Freedman B.I., Langefeld C.D., Rich S.S. et al. Genomics 92:226-234(2008) · Mapped (34) |
| Association analysis of the ephrin-B2 gene in African-Americans with end-stage renal disease. Hicks P.J., Staten J.L., Palmer N.D., Langefeld C.D., Ziegler J.T., Keene K.L., Sale M.M., Bowden D.W., Freedman B.I. Am. J. Nephrol. 28:914-920(2008) · Mapped (2) |
| Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies. Lewis J.P., Palmer N.D., Hicks P.J., Sale M.M., Langefeld C.D., Freedman B.I., Divers J., Bowden D.W. Diabetes 57:2220-2225(2008) · Mapped (41) |
| Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study. Palmer N.D., Goodarzi M.O., Langefeld C.D., Ziegler J., Norris J.M., Haffner S.M., Bryer-Ash M., Bergman R.N., Wagenknecht L.E., Taylor K.D. et al. Diabetes 57:1093-1100(2008) · Mapped (4) |
| Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans. Palmer N.D., Lehtinen A.B., Langefeld C.D., Campbell J.K., Haffner S.M., Norris J.M., Bergman R.N., Goodarzi M.O., Rotter J.I., Bowden D.W. J. Clin. Endocrinol. Metab. 93:304-309(2008) · Mapped (26) |
| The uncoupling protein 1 gene, UCP1, is expressed in mammalian islet cells and associated with acute insulin response to glucose in African American families from the IRAS Family Study. Sale M.M., Hsu F.C., Palmer N.D., Gordon C.J., Keene K.L., Borgerink H.M., Sharma A.J., Bergman R.N., Taylor K.D., Saad M.F. et al. BMC Endocr Disord 7:1-1(2007) · Mapped (3) |
| Association of protein tyrosine phosphatase 1B gene polymorphisms with measures of glucose homeostasis in Hispanic Americans: the insulin resistance atherosclerosis study (IRAS) family study. Palmer N.D., Bento J.L., Mychaleckyj J.C., Langefeld C.D., Campbell J.K., Norris J.M., Haffner S.M., Bergman R.N., Bowden D.W. Diabetes 53:3013-3019(2004) · Mapped (4) |
| Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes. Bento J.L., Palmer N.D., Mychaleckyj J.C., Lange L.A., Langefeld C.D., Rich S.S., Freedman B.I., Bowden D.W. Diabetes 53:3007-3012(2004) · Mapped (4) |
| A bacterial genome in flux: the twelve linear and nine circular extrachromosomal DNAs in an infectious isolate of the Lyme disease spirochete Borrelia burgdorferi. Casjens S., Palmer N., van Vugt R., Huang W.M., Stevenson B., Rosa P., Lathigra R., Sutton G.G., Peterson J.D., Dodson R.J. et al. Mol. Microbiol. 35:490-516(2000) · UniProtKB (312) |
| Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi. Fraser C.M., Casjens S., Huang W.M., Sutton G.G., Clayton R.A., Lathigra R., White O., Ketchum K.A., Dodson R.J., Hickey E.K. et al. Nature 390:580-586(1997) · UniProtKB (1,556) |
