|1.||Ng, Dominic S: 7 articles (12/2015 - 04/2002)|
|2.||Connelly, Philip W: 6 articles (06/2012 - 04/2002)|
|3.||Calabresi, Laura: 5 articles (01/2012 - 06/2004)|
|4.||Katoh, N: 5 articles (06/2001 - 01/2000)|
|5.||Maguire, Graham F: 4 articles (06/2012 - 04/2002)|
|6.||Franceschini, Guido: 4 articles (01/2012 - 06/2004)|
|7.||Santamarina-Fojo, S: 4 articles (12/2001 - 02/2000)|
|8.||Kuroda, Masayuki: 3 articles (08/2014 - 02/2011)|
|9.||Bujo, Hideaki: 3 articles (08/2014 - 02/2011)|
|10.||Schaefer, Ernst J: 3 articles (06/2014 - 08/2008)|
|1.||Lecithin Acyltransferase Deficiency (Lecithin:Cholesterol Acyltransferase Deficiency)
12/01/2013 - "Lecithin:cholesterol acyltransferase replacement therapy showed positive results in a patient with lecithin:cholesterol acyltransferase deficiency. "
12/04/1998 - "Two naturally occurring mutants of human lecithin-cholesterol acyltransferase (LCAT), T123I and N228K, were expressed in COS-1 and Chinese hamster ovary cells, overproduced, and purified to homogeneity in order to study the structural and functional defects that lead to the LCAT deficiency phenotypes of these mutations. "
01/01/1988 - "A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiency."
02/01/1980 - "Study of erythrocytes in a hereditary hemolytic syndrome (HHS): comparison with erythrocytes in lecithin:cholesterol acyltransferase (LCAT) deficiency."
12/01/2011 - "We trace the 34-year history of a member of the first Japanese family in which lecithin-cholesterol acyltransferase (LCAT) deficiency was diagnosed. "
05/01/2000 - "Overexpression of human lecithin:cholesterol acyltransferase in mice offers no protection against diet-induced atherosclerosis."
12/06/2011 - "The aim of this study was to investigate the role of reduced lecithin: cholesterol acyltransferase (LCAT) function on atherogenesis using 3.0-T carotid magnetic resonance imaging (MRI) and B-mode ultrasound. "
12/01/1994 - "This study grew out of observations of certain lecithin:cholesterol acyltransferase (LCAT) abnormalities in patients with atherosclerosis. "
09/01/2012 - "Lecithin:cholesterol acyltransferase: old friend or foe in atherosclerosis?"
12/06/2011 - "Carriers of lecithin cholesterol acyltransferase gene mutations have accelerated atherogenesis as assessed by carotid 3.0-T magnetic resonance imaging [corrected]."
10/01/2014 - "This study aims to evaluate the genetic basis and activity of lecithin cholesterol acyltransferase (LCAT) in a novel Mongolian gerbil model for hyperlipidemia. "
03/01/1979 - "Plasma lecithin:cholesterol acyltransferase (LCAT) activity is increased during the clearance phase of alimentary lipemia induced by a high-fat test meal in normal subjects. "
09/01/1972 - "[Hyperlipemia and plasma lecithin-cholesterol acyltransferase activity]."
11/01/1970 - "Hyperlipemia was also associated with an early increase in plasma lecithin:cholesterol acyltransferase (LCAT) activity in vitro. "
10/01/2002 - "Following consumption of a mixed meal (1200 kcal), plasma-mediated cellular free cholesterol (FC) efflux, lecithin:cholesterol acyltransferase (LCAT), and cholesteryl ester transfer protein (CETP) activities were determined in subjects (n = 12) displaying type IIB hyperlipidemia and compared with those in a normolipidemic control group (n = 14). "
01/01/2015 - "Familial lecithin-cholesterol acyltransferase (LCAT) deficiency; a differential of proteinuria."
01/01/1993 - "The molecular defects in the lecithin:cholesterol acyltransferase (LCAT) gene have been identified in a 52-year-old patient with classic LCAT deficiency, presenting with corneal clouding and proteinuria. "
05/03/1969 - "A WOMAN WITH FAMILIAL PLASMA LECITHIN: cholesterol acyltransferase (L.C.A.T.) deficiency showed, like the other reported cases, obvious corneal opacity, proteinuria, and moderate anaemia with a slight haemolytic component. "
01/01/2011 - "Sex dimorphism in serum lecithin: cholesterol acyltransferase and lipoprotein lipase activities in adult sickle cell anaemia patients with proteinuria."
03/01/1987 - "Familial lecithin: cholesterol acyltransferase (LCAT) deficiency is an inborn error of lipid metabolism clinically characterized by anemia, proteinuria, and corneal opacification. "
04/01/2003 - "(3) A predictive value of the ratios of fast to slow H-components as an indicator of lecithin:cholesterol acyltransferase activity was demonstrated which tended to decrease at hypertriglyceridemia. "
03/15/1978 - "Lecithin-cholesterol acyltransferase activity in carbohydrate-induced hypertriglyceridemia in mice."
01/01/2006 - "Complete lecithin:cholesterol acyltransferase (LCAT) deficiency is associated with fasting hypertriglyceridemia (HTG). "
04/03/1978 - "Using exogenous substrate for its assay, lecithin:cholesterol acyltransferase (LCAT) was found to be decreased in liver disease and higher than normal in endogenous hypertriglyceridemia. "
02/27/2004 - "Hypertriglyceridemia in lecithin-cholesterol acyltransferase-deficient mice is associated with hepatic overproduction of triglycerides, increased lipogenesis, and improved glucose tolerance."
|2.||Apolipoprotein A-I (Apolipoprotein A1)
|4.||Apolipoproteins E (ApoE)
|5.||Phospholipid Transfer Proteins
|6.||Scavenger Receptors (Scavenger Receptor)
|7.||ATP-Binding Cassette Transporters (ABC Transporters)
|10.||Lipoprotein Receptors (Lipoprotein Receptor)
|1.||Fat-Restricted Diet (Diet, Fat Restricted)
|3.||Renal Dialysis (Hemodialysis)