Year |
Citation |
Score |
2009 |
White CH, Ohmen JD, Sheth S, Zebboudj AF, McHugh RK, Hoffman LF, Lusis AJ, Davis RC, Friedman RA. Genome-wide screening for genetic loci associated with noise-induced hearing loss. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 20: 207-13. PMID 19337678 DOI: 10.1007/S00335-009-9178-5 |
0.462 |
|
2006 |
Sheth SS, Bodnar JS, Ghazalpour A, Thipphavong CK, Tsutsumi S, Tward AD, Demant P, Kodama T, Aburatani H, Lusis AJ. Hepatocellular carcinoma in Txnip-deficient mice. Oncogene. 25: 3528-36. PMID 16607285 DOI: 10.1038/Sj.Onc.1209394 |
0.629 |
|
2005 |
Ghazalpour A, Doss S, Sheth SS, Ingram-Drake LA, Schadt EE, Lusis AJ, Drake TA. Genomic analysis of metabolic pathway gene expression in mice. Genome Biology. 6: R59. PMID 15998448 DOI: 10.1186/Gb-2005-6-7-R59 |
0.722 |
|
2005 |
Sheth SS, Castellani LW, Chari S, Wagg C, Thipphavong CK, Bodnar JS, Tontonoz P, Attie AD, Lopaschuk GD, Lusis AJ. Thioredoxin-interacting protein deficiency disrupts the fasting-feeding metabolic transition. Journal of Lipid Research. 46: 123-34. PMID 15520447 DOI: 10.1194/Jlr.M400341-Jlr200 |
0.694 |
|
2004 |
Donnelly KL, Margosian MR, Sheth SS, Lusis AJ, Parks EJ. Increased lipogenesis and fatty acid reesterification contribute to hepatic triacylglycerol stores in hyperlipidemic Txnip-/- mice. The Journal of Nutrition. 134: 1475-80. PMID 15173414 DOI: 10.1093/Jn/134.6.1475 |
0.536 |
|
2004 |
Hui TY, Sheth SS, Diffley JM, Potter DW, Lusis AJ, Attie AD, Davis RA. Mice lacking thioredoxin-interacting protein provide evidence linking cellular redox state to appropriate response to nutritional signals. The Journal of Biological Chemistry. 279: 24387-93. PMID 15047687 DOI: 10.1074/Jbc.M401280200 |
0.532 |
|
2002 |
Sheth SS, Deluna A, Allayee H, Lusis AJ. Understanding atherosclerosis through mouse genetics. Current Opinion in Lipidology. 13: 181-9. PMID 11891421 DOI: 10.1097/00041433-200204000-00010 |
0.487 |
|
2002 |
Bodnar JS, Chatterjee A, Castellani LW, Ross DA, Ohmen J, Cavalcoli J, Wu C, Dains KM, Catanese J, Chu M, Sheth SS, Charugundla K, Demant P, West DB, de Jong P, et al. Positional cloning of the combined hyperlipidemia gene Hyplip1. Nature Genetics. 30: 110-6. PMID 11753387 DOI: 10.1038/Ng811 |
0.687 |
|
2001 |
Pajukanta P, Bodnar JS, Sallinen R, Chu M, Airaksinen T, Xiao Q, Castellani LW, Sheth SS, Wessman M, Palotie A, Sinsheimer JS, Demant P, Lusis AJ, Peltonen L. Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 238-45. PMID 11252174 DOI: 10.1007/S003350010265 |
0.664 |
|
Show low-probability matches. |