Complete and Partial LCAT Deficiency Are Differentially Associated With Atherosclerosis

Circulation - United States
doi 10.1161/circulationaha.118.034706
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Ovid Technologies (Wolters Kluwer Health)

Related search

Familial LCAT Deficiency

2020English

Partial and Complete SPINK1 Deficiency Cause Distinct Pancreatic Phenotypes

Human Mutation
Genetics
2017English

Two Novel Molecular Defects in the LCAT Gene Are Associated With Fish Eye Disease

Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular MedicineCardiology
1996English

Japanese Family With a Deficiency of Lecithin: Cholesterol Acyltransferase (LCAT).

Internal Medicine
Internal MedicineMedicine
1994English

Presumptive Mosaic Partial Trisomy Associated With Congenital Anomalies and Mental Deficiency

Journal of Medical Genetics
Genetics
1974English

The Analysis of Plasma Apo E in Normal, LPL Deficiency and Lcat Deficiency

The Journal of Japan Atherosclerosis Society
1982English

A Proteomic Approach to Identify Novel Disease Biomarkers in LCAT Deficiency

Journal of Proteomics
BiochemistryBiophysics
2019English

Differentially Methylated Loci in NAFLD Cirrhosis Are Associated With Key Signaling Pathways

Clinical Epigenetics
GeneticsDevelopmental BiologyMolecular Biology
2018English

Cognitive-Affective Depression and Somatic Symptoms Clusters Are Differentially Associated With Maternal Parenting and Coparenting

Journal of Affective Disorders
PsychiatryClinical PsychologyMental Health
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy