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Abbreviation : CER
Long Form : cholesterol esterification rate
No. Year Title Co-occurring Abbreviation
2018 Elevated level of lecithin:cholesterol acyltransferase (LCAT) is associated with reduced coronary atheroma burden. CAD, HDL, IVUS, LCAT, RCT
2016 Persistent changes in lipoprotein lipids after a single infusion of ascending doses of MDCO-216 (apoA-IMilano/POPC) in healthy volunteers and stable coronary artery disease patients. APOE, ASOI, CAD, CE, FC, HDL, LDL, PL, SR-BI, TG, VLDL
2006 LCAT deficiency: molecular and phenotypic characterization of an Italian family. LCAT, RCT
2005 Apolipoprotein E is the major physiological activator of lecithin-cholesterol acyltransferase (LCAT) on apolipoprotein B lipoproteins. CE, FC, FPLC, LCAT, LDL, VLDL
2005 Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes. LCAT, LDLR
2003 A novel LCAT mutation (Phe382-->Val) in a kindred with familial LCAT deficiency and defective apolipoprotein B-100. CHD, LCAT
2001 Plasma cholesteryl ester transfer protein and lipoprotein levels during treatment of growth hormone-deficient adult humans. CETP, GH, HDL2, hrGH, LDL-C
2000 High-density lipoprotein cholesterol esterification and transfer rates to lighter density lipoproteins mediated by cholesteryl ester transfer protein in the fasting and postprandial periods are not altered in type 1 diabetes mellitus. CETA, CETP, TG
1999 Plasma cholesterol esterification and transfer, the menopause, and hormone replacement therapy in women. NCET
10  1999 [Correlations of lipoprotein metabolism indicators in persons with low and high cholesterol ester transport activity]. CETA, CHD, HLP
11  1998 Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband. LCAT
12  1995 Triglycerides are major determinants of cholesterol esterification/transfer and HDL remodeling in human plasma. CE, CETP, CETR, LCAT, NL
13  1995 Two novel point mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in LCAT deficiency: LCAT (G873 deletion) and LCAT (Gly344-->Ser). GGT, LCAT