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Apolipoprotein CI Measurement

Known as: APOC1, Apolipoprotein CI 
The determination of the apolipoprotein CI present in a sample.
National Institutes of Health

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3 relations
CDISC SDTM Laboratory Test Terminology by CodeCDISC SDTM Laboratory Test Terminology by NameClinical Data Interchange Standards Consortium Terminology

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
[Analysis of rs4420638A/G and -317H1/H2 polymorphisms of APOC1 gene among Chinese patients with pre-eclampsia].
OBJECTIVE To assess the association of apolipoprotein (apo) C1 (APOC1) gene rs4420638A/G and -317H1/H2 polymorphisms with the… 
2016
2016
Plasma apolipoprotein C1 concentration is associated with plasma triglyceride concentration, but not visceral fat, in patients with type 2 diabetes.
2015
2015
Abstract P2-03-11: Interaction between smoking history and gene expression levels impacts survival of breast carcinoma patients
Our investigations explore the association of cigarette smoking on breast cancer risk of recurrence and progression, in contrast… 
2014
2014
Association of APOC1 and APOE Polymorphism with Alzheimer’s disease: Findings from a Case-Control Study and Meta-Analysis.
2013
2013
Méthodes et kits pour le pronostic du cancer colorectal
L'invention concerne des methodes pour predire le risque de rechute des patients souffrant d'un cancer colorectal, ainsi que des… 
2010
2010
Análise de Polimorfismos nos Genes APOC1, APOC2 e APOC4 e sua Influência no Perfil Lipídico de Crianças e Adolescentes
2007
2007
Discovering multiple transcripts of human hepatocytes using massively parallel signature sequencing (MPSS)
BackgroundThe liver is the largest human internal organ – it is composed of multiple cell types and plays a vital role in… 
2002
2002
Relationship among 1H-magnetic resonance spectroscopy, brain volumetry and genetic polymorphisms in humans with memory impairment
1997
1997
Use of transgenic mice in lipoprotein metabolism and atherosclerosis research.
1989
1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19
SummaryLinkage analysis has been carried out in six German families with autosomal dominantly inherited myotonia congenita… 
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