Related references
Note: Only part of the references are listed.A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient
Liang-Liang Fan et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2019)
A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family
Marianna Maranghi et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2019)
Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope
Liang-Liang Fan et al.
JOURNAL OF HUMAN GENETICS (2019)
Increased Reticulon 3 (RTN3) Leads to Obesity and Hypertriglyceridemia by Interacting With Heat Shock Protein Family A (Hsp70) Member 5 (HSPA5)
Rong Xiang et al.
CIRCULATION (2018)
ATP-Binding Cassette Transporter A Subfamily 8 Is a Sinusoidal Efflux Transporter for Cholesterol and Taurocholate in Mouse and Human Liver
Kazunari Sasaki et al.
MOLECULAR PHARMACEUTICS (2018)
Atherosclerosis A Chronic Inflammatory Disease With an Autoimmune Component
Kouji Kobiyama et al.
CIRCULATION RESEARCH (2018)
ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol Levels
Laia Trigueros-Motos et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2017)
The genetic spectrum of familial hypercholesterolemia in the central south region of China
Rong Xiang et al.
ATHEROSCLEROSIS (2017)
Atherosclerosis Successes, Surprises, and Future Challenges
Peter Libby et al.
CIRCULATION RESEARCH (2016)
Epidemiology of Atherosclerosis and the Potential to Reduce the Global Burden of Atherothrombotic Disease
William Herrington et al.
CIRCULATION RESEARCH (2016)
The Different Facets of Dyslipidemia and Hypertension in Atherosclerosis
Jessica Hurtubise et al.
CURRENT ATHEROSCLEROSIS REPORTS (2016)
Frequent down-regulation of ABC transporter genes in prostate cancer
Rita Demidenko et al.
BMC CANCER (2015)
The Agenda for Familial Hypercholesterolemia A Scientific Statement From the American Heart Association
Samuel S. Gidding et al.
CIRCULATION (2015)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Discovery of microarray-identified genes associated with ovarian cancer progression
Xia Liu et al.
INTERNATIONAL JOURNAL OF ONCOLOGY (2015)
ABCA Transporter Gene Expression and Poor Outcome in Epithelial Ovarian Cancer
Ellen L. Hedditch et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2014)
MutationTaster2: mutation prediction for the deep-sequencing age
Jana Marie Schwarz et al.
NATURE METHODS (2014)
ABCA8 stimulates sphingomyelin production in oligodendrocytes
Woojin Scott Kim et al.
BIOCHEMICAL JOURNAL (2013)
Increased Expression of ABCA8 in Multiple System Atrophy Brain is Associated with Changes in Pathogenic Proteins
Jonathan M. Bleasel et al.
JOURNAL OF PARKINSONS DISEASE (2013)
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia
R. P. Surendran et al.
JOURNAL OF INTERNAL MEDICINE (2012)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich et al.
NATURE (2010)
The Residual Risk Reduction Initiative: A Call to Action to Reduce Residual Vascular Risk in Patients with Dyslipidemia
Jean-Charles Fruchart et al.
AMERICAN JOURNAL OF CARDIOLOGY (2008)
Role of ATP-binding cassette transporters in brain lipid transport and neurological disease
Woojin Scott Kim et al.
JOURNAL OF NEUROCHEMISTRY (2008)
Functional analysis of ABCA8, a new drug transporter
S Tsuruoka et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2002)
ABCA6, a novel A subclass ABC transporter
WE Kaminski et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)
Share Paper
