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ADTRP regulates TFPI expression via transcription factor POU1F1 involved in coronary artery disease

Gene, 2020-08, Vol.753, p.144805-144805, Article 144805

2020

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Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy

Human genetics, 2018-10, Vol.137 (10), p.779-794

2018

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Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies

Journal of the American Heart Association, 2020-04, Vol.9 (7), p.e014146-e014146

2020

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Comparative gene expression analysis between coronary arteries and internal mammary arteries identifies a role for the TES gene in endothelial cell functions relevant to coronary artery disease

Human molecular genetics, 2012-03, Vol.21 (6), p.1364-1373

2012

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Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family

Gene, 2012-01, Vol.491 (2), p.246-250

2012

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Proteomic approach to coronary atherosclerosis shows ferritin light chain as a significant marker: evidence consistent with iron hypothesis in atherosclerosis

Physiological genomics, 2003-03, Vol.13 (1), p.25-30

2003

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Induction of high STAT1 expression in transgenic mice with LQTS and heart failure

Biochemical and biophysical research communications, 2007-06, Vol.358 (2), p.449-454

2007

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Identification of new genes differentially expressed in coronary artery disease by expression profiling

Physiological genomics, 2003-09, Vol.15 (1), p.65-74

2003

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Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes

The Journal of biological chemistry, 2019-03, Vol.294 (11), p.3881-3898

2019

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Abstract 527: The Functional Significance of the Adenosine A 2b Receptor in the Internal Mammary Artery

Arteriosclerosis, thrombosis, and vascular biology, 2017-05, Vol.37 (suppl_1)

2017

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Splice variants of lncRNA RNA ANRIL exert opposing effects on endothelial cell activities associated with coronary artery disease

RNA biology, 2020-10, Vol.17 (10), p.1391-1401

2020

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Expression profiling of cardiovascular disease

Human genomics, 2004-08, Vol.1 (5), p.355-370

2004

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Role of epigenetic m6A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR‐AKT signaling

The FASEB journal, 2021-05, Vol.35 (5), p.n/a

2021

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Role of epigenetic m 6 A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signaling

The FASEB journal, 2021-05, Vol.35 (5), p.e21465

2021

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Identification of three mutations in the MVK gene in six patients associated with disseminated superficial actinic porokeratosis

Clinica chimica acta, 2016-02, Vol.454, p.124-129

2016

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Correction: Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes

The Journal of biological chemistry, 2019-05, Vol.294 (22), p.8715-8715

2019

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Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria

Journal of investigative dermatology, 2013-09, Vol.133 (9), p.2221-2228

2013

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Microarray analysis of cardiovascular diseases

Methods in molecular medicine, 2006, Vol.129, p.1

2006

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pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradation

Cellular signalling, 2015-11, Vol.27 (11), p.2314-2323

2015

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Analysis of causal effect of APOA5 variants on premature coronary artery disease

Annals of human genetics, 2018-11, Vol.82 (6), p.437-447

2018

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Role of epigenetic m6 A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signaling

The FASEB journal, 2021-05, Vol.35 (5), p.e21465-e21465

2021

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HSF4 is involved in DNA damage repair through regulation of Rad51

Biochimica et biophysica acta, 2012-08, Vol.1822 (8), p.1308-1315

2012

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Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa

Molecular vision, 2016-03, Vol.22, p.234-242

2016

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A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene

Circulation. Cardiovascular genetics, 2014-08, Vol.7 (4), p.514-520

2014

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A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family

Neuroscience letters, 2011-09, Vol.503 (1), p.27-30

2011

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ADTRP regulates TFPI expression via transcription factor POU1F1 involved in coronary artery disease

Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy

Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies

Comparative gene expression analysis between coronary arteries and internal mammary arteries identifies a role for the TES gene in endothelial cell functions relevant to coronary artery disease

Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family

Proteomic approach to coronary atherosclerosis shows ferritin light chain as a significant marker: evidence consistent with iron hypothesis in atherosclerosis

Induction of high STAT1 expression in transgenic mice with LQTS and heart failure

Identification of new genes differentially expressed in coronary artery disease by expression profiling

Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes

Abstract 527: The Functional Significance of the Adenosine A 2b Receptor in the Internal Mammary Artery

Splice variants of lncRNA RNA ANRIL exert opposing effects on endothelial cell activities associated with coronary artery disease

Expression profiling of cardiovascular disease

Role of epigenetic m6A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR‐AKT signaling

Role of epigenetic m 6 A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signaling

Identification of three mutations in the MVK gene in six patients associated with disseminated superficial actinic porokeratosis

Correction: Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes

Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria

Microarray analysis of cardiovascular diseases

pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradation

Analysis of causal effect of APOA5 variants on premature coronary artery disease

Role of epigenetic m6 A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signaling

HSF4 is involved in DNA damage repair through regulation of Rad51

Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa

A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family

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