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69 related items for PubMed ID: 1301939
1. Human hepatic lipase mutations and polymorphisms. Hegele RA, Tu L, Connelly PW. Hum Mutat; 1992; 1(4):320-4. PubMed ID: 1301939 [Abstract] [Full Text] [Related]
2. Relationship between a novel polymorphism of hepatic lipase gene and coronary artery disease. Su ZG, Zhang SZ, Hou YP, Zhang L, Huang DJ, Liao LC, Xiao CY. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai); 2002 Nov; 34(6):780-5. PubMed ID: 12417924 [Abstract] [Full Text] [Related]
3. Molecular characterization of human hepatic lipase deficiency. In vitro expression of two naturally occurring mutations. Durstenfeld A, Ben-Zeev O, Reue K, Stahnke G, Doolittle MH. Arterioscler Thromb; 1994 Mar; 14(3):381-5. PubMed ID: 8123642 [Abstract] [Full Text] [Related]
4. Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels. de Knijff P, van den Maagdenberg AM, Frants RR, Havekes LM. Hum Mutat; 1994 Mar; 4(3):178-94. PubMed ID: 7833947 [Abstract] [Full Text] [Related]
12. Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia. Evans D, Arzer J, Aberle J, Beil FU. Atherosclerosis; 2011 Feb; 214(2):386-90. PubMed ID: 21159338 [Abstract] [Full Text] [Related]
13. C-514T polymorphism in hepatic lipase gene promoter is associated with elevated triglyceride levels and decreasing insulin sensitivity in nondiabetic Japanese subjects. Yabu Y, Noma K, Nakatani K, Nishioka J, Suematsu M, Katsuki A, Hori Y, Yano Y, Sumida Y, Wada H, Nobori T. Int J Mol Med; 2005 Sep; 16(3):421-5. PubMed ID: 16077949 [Abstract] [Full Text] [Related]
16. Effects of hepatic lipase gene promoter nucleotide variations on serum HDL cholesterol concentration in the general Japanese population. Inazu A, Nishimura Y, Terada Y, Mabuchi H. J Hum Genet; 2001 Sep; 46(4):172-7. PubMed ID: 11322655 [Abstract] [Full Text] [Related]
17. Transient induction of a variant hepatic lipase messenger RNA by corticotropic hormone in rat adrenals. Botma GJ, Vieira D, Heuveling M, Jansen H, Verhoeven AJ. Metabolism; 2006 Apr; 55(4):467-77. PubMed ID: 16546477 [Abstract] [Full Text] [Related]
18. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene. Wang D, Wu B, Li Y, Heng W, Zhong H, Mu Y, Wang J. J Hum Genet; 2001 Apr; 46(3):152-4. PubMed ID: 11310584 [Abstract] [Full Text] [Related]
19. Mutations of the human hepatic lipase gene in patients with combined hypertriglyceridemia/hyperalphalipoproteinemia and in patients with familial combined hyperlipidemia. Gehrisch S, Kostka H, Tiebel M, Patzak A, Paetzold A, Julius U, Schroeder HE, Hanefeld M, Jaross W. J Mol Med (Berl); 1999 Oct; 77(10):728-34. PubMed ID: 10606208 [Abstract] [Full Text] [Related]
20. Improved detection of cystic fibrosis mutations in infertility patients with DNA sequence analysis. Danziger KL, Black LD, Keiles SB, Kammesheidt A, Turek PJ. Hum Reprod; 2004 Mar; 19(3):540-6. PubMed ID: 14998948 [Abstract] [Full Text] [Related] Page: [Next] [New Search]