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Page 1
Activity of the anthelmintic benzimidazoles against Giardia lamblia in vitro.
Edlind TD, Hang TL, Chakraborty PR. Edlind TD, et al. Among authors: hang tl. J Infect Dis. 1990 Dec;162(6):1408-11. doi: 10.1093/infdis/162.6.1408. J Infect Dis. 1990. PMID: 2230276
Effect of the hypoglycaemic drug (-)-AZ-DF-265 on ATP-sensitive potassium channels in rat pancreatic beta-cells.
Ronner P, Hang TL, Kraebber MJ, Higgins TJ. Ronner P, et al. Among authors: hang tl. Br J Pharmacol. 1992 Jun;106(2):250-5. doi: 10.1111/j.1476-5381.1992.tb14324.x. Br J Pharmacol. 1992. PMID: 1393260 Free PMC article.
Variation in the gene for muscle-specific AMP deaminase is associated with insulin clearance, a highly heritable trait.
Goodarzi MO, Taylor KD, Guo X, QuiƱones MJ, Cui J, Li X, Hang T, Yang H, Holmes E, Hsueh WA, Olefsky J, Rotter JI. Goodarzi MO, et al. Diabetes. 2005 Apr;54(4):1222-7. doi: 10.2337/diabetes.54.4.1222. Diabetes. 2005. PMID: 15793265
Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease.
Abreu MT, Taylor KD, Lin YC, Hang T, Gaiennie J, Landers CJ, Vasiliauskas EA, Kam LY, Rojany M, Papadakis KA, Rotter JI, Targan SR, Yang H. Abreu MT, et al. Gastroenterology. 2002 Sep;123(3):679-88. doi: 10.1053/gast.2002.35393. Gastroenterology. 2002. PMID: 12198692
A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews.
Sugimura K, Taylor KD, Lin YC, Hang T, Wang D, Tang YM, Fischel-Ghodsian N, Targan SR, Rotter JI, Yang H. Sugimura K, et al. Am J Hum Genet. 2003 Mar;72(3):509-18. doi: 10.1086/367848. Epub 2003 Feb 7. Am J Hum Genet. 2003. PMID: 12577202 Free PMC article.
Candidate locus for a nuclear modifier gene for maternally inherited deafness.
Bykhovskaya Y, Estivill X, Taylor K, Hang T, Hamon M, Casano RA, Yang H, Rotter JI, Shohat M, Fischel-Ghodsian N. Bykhovskaya Y, et al. Am J Hum Genet. 2000 Jun;66(6):1905-10. doi: 10.1086/302914. Epub 2000 Apr 27. Am J Hum Genet. 2000. PMID: 10788333 Free PMC article.
A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14.
Steiner C, Ehtesham N, Taylor KD, Sebald E, Cantor R, King LM, Guo X, Hang T, Hu MS, Cui JR, Friedman B, Norato D, Allanson J, Honeywell C, Mettler G, Field F, Lachman R, Cohn DH, Krakow D. Steiner C, et al. J Med Genet. 2004 Apr;41(4):266-9. doi: 10.1136/jmg.2003.012252. J Med Genet. 2004. PMID: 15060099 Free PMC article.
Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness.
Bykhovskaya Y, Yang H, Taylor K, Hang T, Tun RY, Estivill X, Casano RA, Majamaa K, Shohat M, Fischel-Ghodsian N. Bykhovskaya Y, et al. Genet Med. 2001 May-Jun;3(3):177-80. doi: 10.1097/00125817-200105000-00005. Genet Med. 2001. PMID: 11388757
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