|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0015576,
umls-concept:C0023195,
umls-concept:C0039082,
umls-concept:C0205474,
umls-concept:C0337810,
umls-concept:C0445356,
umls-concept:C1521991,
umls-concept:C1853126,
umls-concept:C1880156,
umls-concept:C2603343,
umls-concept:C2607943,
umls-concept:C2926606
|
|
pubmed:issue |
9
|
|
pubmed:dateCreated |
2005-8-29
|
|
pubmed:abstractText |
To better understand the role of lecithin:cholesterol acyltransferase (LCAT) in lipoprotein metabolism through the genetic and biochemical characterization of families carrying mutations in the LCAT gene.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
1524-4636
|
|
pubmed:author |
pubmed-author:AlessandriniPaolaP,
pubmed-author:ArcaMarcelloM,
pubmed-author:BertoliniStefanoS,
pubmed-author:BonGabriele BittoloGB,
pubmed-author:BoscuttiGiulianoG,
pubmed-author:Brisson-CarrollGiseleG,
pubmed-author:BusnachGhilG,
pubmed-author:CalabresiLauraL,
pubmed-author:CalandraSebastianoS,
pubmed-author:CantaforaAlfredoA,
pubmed-author:CostantinAnnaA,
pubmed-author:EberiniIvanoI,
pubmed-author:FranceschiniGuidoG,
pubmed-author:FrascàGiovanniG,
pubmed-author:GesualdoLoretoL,
pubmed-author:GiganteMaddalenaM,
pubmed-author:LupattelliGrazianaG,
pubmed-author:MontaliAnnaA,
pubmed-author:PisciottaLiviaL,
pubmed-author:PizzolittoStefanoS,
pubmed-author:RabboneIvanaI,
pubmed-author:RolleriMarinaM,
pubmed-author:RuotoloGiacomoG,
pubmed-author:SampietroTizianaT,
pubmed-author:SessaAdalbertoA,
pubmed-author:VaudoGaetanoG,
pubmed-author:VegliaFabrizioF
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
25
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1972-8
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:15994445-Adult,
pubmed-meshheading:15994445-Aged,
pubmed-meshheading:15994445-Atherosclerosis,
pubmed-meshheading:15994445-Cholesterol,
pubmed-meshheading:15994445-Corneal Opacity,
pubmed-meshheading:15994445-Diagnosis, Differential,
pubmed-meshheading:15994445-Esterification,
pubmed-meshheading:15994445-Family Health,
pubmed-meshheading:15994445-Female,
pubmed-meshheading:15994445-Gene Dosage,
pubmed-meshheading:15994445-Genotype,
pubmed-meshheading:15994445-Humans,
pubmed-meshheading:15994445-Italy,
pubmed-meshheading:15994445-Lecithin Acyltransferase Deficiency,
pubmed-meshheading:15994445-Lipoproteins,
pubmed-meshheading:15994445-Male,
pubmed-meshheading:15994445-Middle Aged,
pubmed-meshheading:15994445-Mutation,
pubmed-meshheading:15994445-Pedigree,
pubmed-meshheading:15994445-Phosphatidylcholine-Sterol O-Acyltransferase,
pubmed-meshheading:15994445-Triglycerides
|
|
pubmed:year |
2005
|
|
pubmed:articleTitle |
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families.
|
|
pubmed:affiliation |
Center E. Grossi Paoletti, Department of Pharmacological Sciences, University of Milano, 20133 Milan, Italy.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
