| Association of sequence variations in vitamin K epoxide reductase and gamma-glutamyl carboxylase genes with biochemical measures of vitamin K status. Crosier M.D., Peter I., Booth S.L., Bennett G., Dawson-Hughes B., Ordovas J.M.
J. Nutr. Sci. Vitaminol. 55:112-119(2009) · Mapped (9) |
| Mclk1+/- mice are not resistant to the development of atherosclerosis. Hughes B.G., Hekimi S.
Lipids Health Dis 8:16-16(2009) · Mapped (9) |
| Steroid production and excretion by the pregnant mouse, particularly in relation to pregnancies with fetuses deficient in Delta7-sterol reductase (Dhcr7), the enzyme associated with Smith-Lemli-Opitz syndrome. Matabosch X., Rahman M., Hughes B., Patel S.B., Watson G., Shackleton C.
J. Steroid Biochem. Mol. Biol. 116:61-70(2009) · Mapped (4) |
| Matrix Gla protein polymorphisms are associated with coronary artery calcification in men. Crosier M.D., Booth S.L., Peter I., Dawson-Hughes B., Price P.A., O'Donnell C.J., Hoffmann U., Williamson M.K., Ordovas J.M.
J. Nutr. Sci. Vitaminol. 55:59-65(2009) · Mapped (1) |
| Association between serum osteocalcin and markers of metabolic phenotype. Pittas A.G., Harris S.S., Eliades M., Stark P., Dawson-Hughes B.
J. Clin. Endocrinol. Metab. 94:827-832(2009) · Mapped (1) |
| Hepatic 11beta-HSD1 mRNA expression in fatty liver and nonalcoholic steatohepatitis. Konopelska S., Kienitz T., Hughes B., Pirlich M., Bauditz J., Lochs H., Strasburger C.J., Stewart P.M., Quinkler M.
Clin. Endocrinol. (Oxf) 70:554-560(2009) · Mapped (2) |
| Impaired glucose tolerance and insulin resistance are associated with increased adipose 11beta-hydroxysteroid dehydrogenase type 1 expression and elevated hepatic 5alpha-reductase activity. Tomlinson J.W., Finney J., Gay C., Hughes B.A., Hughes S.V., Stewart P.M.
Diabetes 57:2652-2660(2008) · Mapped (1) |
| Further support for association of the mitochondrial complex I subunit gene NDUFV2 with bipolar disorder. Xu C., Li P.P., Kennedy J.L., Green M., Hughes B., Cooke R.G., Parikh S.V., Warsh J.J.
Bipolar Disord 10:105-110(2008) · Mapped (6) |
| Modulation of the Kir7.1 potassium channel by extracellular and intracellular pH. Hughes B.A., Swaminathan A.
Am. J. Physiol., Cell Physiol. 294:C423-31(2008) · Mapped (3) |
| Expression of Kir7.1 and a novel Kir7.1 splice variant in native human retinal pigment epithelium. Yang D., Swaminathan A., Zhang X., Hughes B.A.
Exp. Eye Res. 86:81-91(2008) · UniProtKB (2) · Mapped (1) |
| Reduced 11beta-hydroxysteroid dehydrogenase type 1 activity in obese boys. Wiegand S., Richardt A., Remer T., Wudy S.A., Tomlinson J.W., Hughes B., Gruters A., Stewart P.M., Strasburger C.J., Quinkler M.
Eur. J. Endocrinol. 157:319-324(2007) · Mapped (1) |
| 11beta-Hydroxysteroid Dehydrogenase Type 1 Regulation by Intracellular Glucose 6-Phosphate Provides Evidence for a Novel Link between Glucose Metabolism and Hypothalamo-Pituitary-Adrenal Axis Function. Walker E.A., Ahmed A., Lavery G.G., Tomlinson J.W., Kim S.Y., Cooper M.S., Ride J.P., Hughes B.A., Shackleton C.H., McKiernan P. et al.
J. Biol. Chem. 282:27030-27036(2007) · Mapped (9) |
| Specific expression of lacZ and cre recombinase in fetal thymic epithelial cells by multiplex gene targeting at the Foxn1 locus. Gordon J., Xiao S., Hughes B., Su D.M., Navarre S.P., Condie B.G., Manley N.R.
BMC Dev. Biol. 7:69-69(2007) · Mapped (7) |
| Spatial and temporal expression of MFRP and its interaction with CTRP5. Mandal M.N., Vasireddy V., Jablonski M.M., Wang X., Heckenlively J.R., Hughes B.A., Reddy G.B., Ayyagari R.
Invest. Ophthalmol. Vis. Sci. 47:5514-5521(2006) · Mapped (2) |
| CTRP5 is a membrane-associated and secretory protein in the RPE and ciliary body and the S163R mutation of CTRP5 impairs its secretion. Mandal M.N., Vasireddy V., Reddy G.B., Wang X., Moroi S.E., Pattnaik B.R., Hughes B.A., Heckenlively J.R., Hitchcock P.F., Jablonski M.M. et al.
Invest. Ophthalmol. Vis. Sci. 47:5505-5513(2006) · Mapped (15) |
| Matrix Gla protein is associated with risk factors for atherosclerosis but not with coronary artery calcification. O'Donnell C.J., Shea M.K., Price P.A., Gagnon D.R., Wilson P.W., Larson M.G., Kiel D.P., Hoffmann U., Ferencik M., Clouse M.E. et al.
Arterioscler. Thromb. Vasc. Biol. 26:2769-2774(2006) · Mapped (2) |
| Genetic and molecular characterization of CLK-1/mCLK1, a conserved determinant of the rate of aging. Stepanyan Z., Hughes B., Cliche D.O., Camp D., Hekimi S.
Exp. Gerontol. 41:940-951(2006) · Mapped (1) |
| Functional complementation of truncated human skeletal-muscle chloride channel (hClC-1) using carboxyl tail fragments. Wu W., Rychkov G.Y., Hughes B.P., Bretag A.H.
Biochem. J. 395:89-97(2006) · Mapped (2) |
| Functional genomic analysis of the AUXIN/INDOLE-3-ACETIC ACID gene family members in Arabidopsis thaliana. Overvoorde P.J., Okushima Y., Alonso J.M., Chan A., Chang C., Ecker J.R., Hughes B., Liu A., Onodera C., Quach H. et al.
Plant Cell 17:3282-3300(2005) · UniProtKB (2) · Mapped (16) |
| Association of the putative susceptibility gene, transient receptor potential protein melastatin type 2, with bipolar disorder. Xu C., Macciardi F., Li P.P., Yoon I.S., Cooke R.G., Hughes B., Parikh S.V., McIntyre R.S., Kennedy J.L., Warsh J.J.
Am. J. Med. Genet. B Neuropsychiatr. Genet. 141B:36-43(2006) · Mapped (5) |
| Evolutionary conservation of the clk-1-dependent mechanism of longevity: loss of mclk1 increases cellular fitness and lifespan in mice. Liu X., Jiang N., Hughes B., Bigras E., Shoubridge E., Hekimi S.
Genes Dev. 19:2424-2434(2005) · Mapped (3) |
| Functional genomic analysis of the AUXIN RESPONSE FACTOR gene family members in Arabidopsis thaliana: unique and overlapping functions of ARF7 and ARF19. Okushima Y., Overvoorde P.J., Arima K., Alonso J.M., Chan A., Chang C., Ecker J.R., Hughes B., Lui A., Nguyen D. et al.
Plant Cell 17:444-463(2005) · UniProtKB (14) · Mapped (14) |
| Toll-like receptor 4 (TLR4) of retinal pigment epithelial cells participates in transmembrane signaling in response to photoreceptor outer segments. Kindzelskii A.L., Elner V.M., Elner S.G., Yang D., Hughes B.A., Petty H.R.
J. Gen. Physiol. 124:139-149(2004) · Mapped (1) |
| Characterization of three myotonia-associated mutations of the CLCN1 chloride channel gene via heterologous expression. Simpson B.J., Height T.A., Rychkov G.Y., Nowak K.J., Laing N.G., Hughes B.P., Bretag A.H.
Hum. Mutat. 24:185-185(2004) · Mapped (2) |
| Preliminary investigation into the expression of proton-coupled oligopeptide transporters in neural retina and retinal pigment epithelium (RPE): lack of functional activity in RPE plasma membranes. Ocheltree S.M., Keep R.F., Shen H., Yang D., Hughes B.A., Smith D.E.
Pharm. Res. 20:1364-1372(2003) · UniProtKB (1) |
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