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miR‐195 reduces age‐related blood–brain barrier leakage caused by thrombospondin‐1‐mediated selective autophagy

Aging cell, 2020-11, Vol.19 (11), p.e13236-n/a

2020

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TRPV4 Activation Contributes Functional Recovery from Ischemic Stroke via Angiogenesis and Neurogenesis

Molecular neurobiology, 2018-05, Vol.55 (5), p.4127-4135

2018

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microRNA let‐7g suppresses PDGF‐induced conversion of vascular smooth muscle cell into the synthetic phenotype

Journal of cellular and molecular medicine, 2017-12, Vol.21 (12), p.3592-3601

2017

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In-utero epigenetic factors are associated with early-onset myopia in young children

PloS one, 2019-05, Vol.14 (5), p.e0214791-e0214791

2019

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Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke

PloS one, 2015-09, Vol.10 (9), p.e0139608-e0139608

2015

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miR-195 Has a Potential to Treat Ischemic and Hemorrhagic Stroke through Neurovascular Protection and Neurogenesis

Molecular therapy. Methods & clinical development, 2019-06, Vol.13, p.121-132

2019

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MicroRNA let‐7g possesses a therapeutic potential for peripheral artery disease

Journal of cellular and molecular medicine, 2017-03, Vol.21 (3), p.519-529

2017

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PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese Population

Frontiers in genetics, 2022-01, Vol.12, p.775797-775797

2022

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Cerebral Semaphorin3D is a novel risk factor for age-associated cognitive impairment

Cell communication and signaling, 2023-06, Vol.21 (1), p.140-140, Article 140

2023

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LINE-1 methylation is associated with an increased risk of ischemic stroke in men

Current neurovascular research, 2014-02, Vol.11 (1), p.4-9

2014

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The risk of the metabolic syndrome on carotid thickness and stiffness: Sex and age specific effects

Atherosclerosis, 2010-05, Vol.210 (1), p.155-159

2010

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Early functional improvement after stroke correlates with cardiovascular fitness

The Kaohsiung journal of medical sciences, 2018-11, Vol.34 (11), p.643-649

2018

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HOXA9 is a novel myopia risk gene

BMC ophthalmology, 2019-01, Vol.19 (1), p.28-28, Article 28

2019

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Genetics of carotid atherosclerosis

Frontiers in bioscience, 2009-01, Vol.14 (12), p.4525-4534

Juo, Suh-Hang H

2009

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Carotid atherosclerosis among middle-aged individuals predicts cognition: A 10-year follow-up study

Atherosclerosis, 2020-12, Vol.314, p.27-32

2020

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miR-328-3p Affects Axial Length Via Multiple Routes and Anti-miR-328-3p Possesses a Potential to Control Myopia Progression

Investigative ophthalmology & visual science, 2022-11, Vol.63 (12), p.11-11

2022

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A microRNA-520 mirSNP at the MMP2 gene influences susceptibility to endometriosis in Chinese women

Journal of human genetics, 2013-04, Vol.58 (4), p.202-209

2013

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Determinants of arterial stiffness progression in a Han-Chinese population in Taiwan: a 4-year longitudinal follow-up

BMC cardiovascular disorders, 2015-09, Vol.15 (1), p.100-100, Article 100

2015

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MicroRNA Therapy for Dry Eye Disease

Journal of ocular pharmacology and therapeutics, 2022-03, Vol.38 (2), p.125-132

2022

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Methylation in the matrix metalloproteinase-2 gene is associated with cerebral ischemic stroke

Journal of investigative medicine, 2017-04, Vol.65 (4), p.794-799

2017

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Let-7g suppresses both canonical and non-canonical NF-κB pathways in macrophages leading to anti-atherosclerosis

Oncotarget, 2017-11, Vol.8 (60), p.101026-101041

2017

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A functional polymorphism of PON1 interferes with microRNA binding to increase the risk of ischemic stroke and carotid atherosclerosis

Atherosclerosis, 2013-05, Vol.228 (1), p.161-167

2013

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MicroRNA let-7g inhibits angiotensin II-induced endothelial senescence via the LOX-1-independent mechanism

International journal of molecular medicine, 2018-04, Vol.41 (4), p.2243-2251

2018

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SNPs in BRAP associated with risk of myocardial infarction in Asian populations

Nature genetics, 2009-03, Vol.41 (3), p.329-333

2009

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SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

Journal of human genetics, 2011-01, Vol.56 (1), p.47-51

2011

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miR‐195 reduces age‐related blood–brain barrier leakage caused by thrombospondin‐1‐mediated selective autophagy

TRPV4 Activation Contributes Functional Recovery from Ischemic Stroke via Angiogenesis and Neurogenesis

microRNA let‐7g suppresses PDGF‐induced conversion of vascular smooth muscle cell into the synthetic phenotype

In-utero epigenetic factors are associated with early-onset myopia in young children

Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke

miR-195 Has a Potential to Treat Ischemic and Hemorrhagic Stroke through Neurovascular Protection and Neurogenesis

MicroRNA let‐7g possesses a therapeutic potential for peripheral artery disease

PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese Population

Cerebral Semaphorin3D is a novel risk factor for age-associated cognitive impairment

LINE-1 methylation is associated with an increased risk of ischemic stroke in men

The risk of the metabolic syndrome on carotid thickness and stiffness: Sex and age specific effects

Early functional improvement after stroke correlates with cardiovascular fitness

HOXA9 is a novel myopia risk gene

Genetics of carotid atherosclerosis

Carotid atherosclerosis among middle-aged individuals predicts cognition: A 10-year follow-up study

miR-328-3p Affects Axial Length Via Multiple Routes and Anti-miR-328-3p Possesses a Potential to Control Myopia Progression

A microRNA-520 mirSNP at the MMP2 gene influences susceptibility to endometriosis in Chinese women

Determinants of arterial stiffness progression in a Han-Chinese population in Taiwan: a 4-year longitudinal follow-up

MicroRNA Therapy for Dry Eye Disease

Methylation in the matrix metalloproteinase-2 gene is associated with cerebral ischemic stroke

Let-7g suppresses both canonical and non-canonical NF-κB pathways in macrophages leading to anti-atherosclerosis

A functional polymorphism of PON1 interferes with microRNA binding to increase the risk of ischemic stroke and carotid atherosclerosis

MicroRNA let-7g inhibits angiotensin II-induced endothelial senescence via the LOX-1-independent mechanism

SNPs in BRAP associated with risk of myocardial infarction in Asian populations

SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population

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