1 - 25 of
131
results
for author:"Hunt S."
in Literature Citations
| Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins. Kollerits B., Coassin S., Beckmann N.D., Teumer A., Kiechl S., Doring A., Kavousi M., Hunt S.C., Lamina C., Paulweber B. et al. Hum. Mol. Genet. 18:4669-4676(2009) · Mapped (1) |
| A common variant in the adiponutrin gene influences liver enzyme levels. Kollerits B., Coassin S., Kiechl S., Hunt S.C., Paulweber B., Willeit J., Brandstatter A., Adams T.D., Kronenberg F. J. Med. Genet. 0:0-0(2009) · Mapped (1) |
| Localization of the endocannabinoid-degrading enzyme fatty acid amide hydrolase in rat dorsal root ganglion cells and its regulation after peripheral nerve injury. Lever I.J., Robinson M., Cibelli M., Paule C., Santha P., Yee L., Hunt S.P., Cravatt B.F., Elphick M.R., Nagy I. et al. J. Neurosci. 29:3766-3780(2009) · Mapped (1) |
| The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study. Franceschini N., North K.E., Arnett D., Pankow J.S., Chung J.H., Baird L., Leppert M.F., Eckfeldt J.H., Boerwinkle E., Gu C.C. et al. Am. J. Hypertens. 22:552-558(2009) · Mapped (4) |
| Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study. Freedman B.I., Kopp J.B., Winkler C.A., Nelson G.W., Rao D.C., Eckfeldt J.H., Leppert M.F., Hicks P.J., Divers J., Langefeld C.D. et al. Am. J. Nephrol. 29:626-632(2009) · Mapped (11) |
| Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype. Type 1 Diabetes Genetics Consortium Diabetes Obes Metab 11 Suppl 1:8-16(2009) · Mapped (884) |
| Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship. Wellcome Trust Case Control Consortium Gastroenterology 136:523-9.e3(2009) · Mapped (55) |
| Variants in MTNR1B influence fasting glucose levels. Prokopenko I., Langenberg C., Florez J.C., Saxena R., Soranzo N., Thorleifsson G., Loos R.J., Manning A.K., Jackson A.U., Aulchenko Y. et al. Nat. Genet. 41:77-81(2009) · Mapped (7) |
| A key role for autophagy and the autophagy gene Atg16l1 in mouse and human intestinal Paneth cells. Cadwell K., Liu J.Y., Brown S.L., Miyoshi H., Loh J., Lennerz J.K., Kishi C., Kc W., Carrero J.A., Hunt S. et al. Nature 456:259-263(2008) · Mapped (14) |
| Regulation of pain sensitivity in experimental osteoarthritis by the endogenous peripheral opioid system. Inglis J.J., McNamee K.E., Chia S.L., Essex D., Feldmann M., Williams R.O., Hunt S.P., Vincent T. Arthritis Rheum. 58:3110-3119(2008) · Mapped (44) |
| Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease. Lingenhel A., Kollerits B., Schwaiger J.P., Hunt S.C., Gress R., Hopkins P.N., Schoenborn V., Heid I.M., Kronenberg F. Exp. Gerontol. 43:1102-1107(2008) · Mapped (6) |
| Association of the melanocortin-4 receptor V103I polymorphism with dietary intake in severely obese persons. Pichler M., Kollerits B., Heid I.M., Hunt S.C., Adams T.D., Hopkins P.N., Kronenberg F. Am. J. Clin. Nutr. 88:797-800(2008) · Mapped (1) |
| Genetic association between aldehyde dehydrogenase 2 (ALDH2) variation and high-density lipoprotein cholesterol (HDL-C) among non-drinkers in two large population samples in Japan. Wada M., Daimon M., Emi M., Iijima H., Sato H., Koyano S., Tajima K., Kawanami T., Kurita K., Hunt S.C. et al. J. Atheroscler. Thromb. 15:179-184(2008) · Mapped (4) |
| Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies. Barroso I., Luan J., Wheeler E., Whittaker P., Wasson J., Zeggini E., Weedon M.N., Hunt S., Venkatesh R., Frayling T.M. et al. Diabetes 57:3161-3165(2008) · Mapped (8) |
| Deletion of the mouse RegIIIbeta (Reg2) gene disrupts ciliary neurotrophic factor signaling and delays myelination of mouse cranial motor neurons. Tebar L.A., Geranton S.M., Parsons-Perez C., Fisher A.S., Bayne R., Smith A.J., Turmaine M., Perez-Luz S., Sheasby A., De Felipe C. et al. Proc. Natl. Acad. Sci. U.S.A. 105:11400-11405(2008) · Mapped (5) |
| Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM. Daimon M., Sato H., Sasaki S., Toriyama S., Emi M., Muramatsu M., Hunt S.C., Hopkins P.N., Karasawa S., Wada K. et al. Biochem. Biophys. Res. Commun. 374:576-580(2008) · Mapped (4) |
| Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI. Brandstatter A., Kiechl S., Kollerits B., Hunt S.C., Heid I.M., Coassin S., Willeit J., Adams T.D., Illig T., Hopkins P.N. et al. Diabetes Care 31:1662-1667(2008) · Mapped (1) |
| Common variants near MC4R are associated with fat mass, weight and risk of obesity. Wellcome Trust Case Control Consortium Nat. Genet. 40:768-775(2008) · Mapped (1) |
| Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. Wellcome Trust Case Control Consortium Nat. Genet. 40:710-712(2008) · Mapped (54) |
| Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol. Love-Gregory L., Sherva R., Sun L., Wasson J., Schappe T., Doria A., Rao D.C., Hunt S.C., Klein S., Neuman R.J. et al. Hum. Mol. Genet. 17:1695-1704(2008) · Mapped (12) |
| Genetic background influences the behavioural and molecular consequences of neurokinin-1 receptor knockout. McCutcheon J.E., Fisher A.S., Guzdar E., Wood S.A., Lightman S.L., Hunt S.P. Eur. J. Neurosci. 27:683-690(2008) · Mapped (3) |
| Neurokinin 1 receptor antagonism as a possible therapy for alcoholism. George D.T., Gilman J., Hersh J., Thorsell A., Herion D., Geyer C., Peng X., Kielbasa W., Rawlings R., Brandt J.E. et al. Science 319:1536-1539(2008) · Mapped (3) |
| Association of the FTO gene with BMI. Hunt S.C., Stone S., Xin Y., Scherer C.A., Magness C.L., Iadonato S.P., Hopkins P.N., Adams T.D. Obesity (Silver Spring) 16:902-904(2008) · Mapped (4) |
| INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolism. Boes E., Kollerits B., Heid I.M., Hunt S.C., Pichler M., Paulweber B., Coassin S., Adams T.D., Hopkins P.N., Lingenhel A. et al. Obesity (Silver Spring) 16:827-833(2008) · Mapped (2) |
| Epithelial polarity requires septin coupling of vesicle transport to polyglutamylated microtubules. Spiliotis E.T., Hunt S.J., Hu Q., Kinoshita M., Nelson W.J. J. Cell Biol. 180:295-303(2008) · UniProtKB (1) |
