Lista de obras -

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

artículo científico publicado el 21 de febrero de 2013

A novel DNAJB6 mutation causes dominantly inherited distal-onset myopathy and compromises DNAJB6 function

artículo científico publicado en 2017

ABCA7 gene and the risk of Alzheimer's disease in Han Chinese in Taiwan

artículo científico publicado en 2014

Characterization of Heterozygous HTRA1 Mutations in Taiwanese Patients With Cerebral Small Vessel Disease

artículo científico publicado en 2018

Chromosome 9p21 Genetic Variants are Associated with Myocardial Infarction but Not with Ischemic Stroke in a Taiwanese Population ⬇️

artículo científico publicado el 1 de agosto de 2011

Circulating microRNAs have a sex-specific association with metabolic syndrome

artículo científico publicado en 2013

Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy.

artículo científico publicado en 2017

Clinical and biophysical characterization of 19 GJB1 mutations.

scientific article published on September 2016

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

scientific article published on 09 April 2019

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

scientific article published on 22 March 2020

Comparable progression of spinocerebellar ataxias between Caucasians and Chinese

artículo científico publicado en 2018

Decreased MicroRNA-221 is Associated with High Levels of TNF-a in Human Adipose Tissue-Derived Mesenchymal Stem Cells From Obese Woman ⬇️

artículo científico publicado el 12 de julio de 2013

Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Elevated circulating endothelial-specific microRNAs in migraine patients: A pilot study.

artículo científico publicado en 2017

Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan

artículo científico publicado en 2018

Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant

artículo científico publicado en 2020

Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis.

artículo científico publicado en 2017

Investigating CYP2C19 loss-of-function allele statuses and their association with stroke of different etiologies in a Taiwanese population

scientific article published on 01 June 2019

Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia

artículo científico publicado en 2019

Juvenile Huntington's disease presenting as difficult-to-treat seizure and the first episode of psychosis ⬇️

artículo científico publicado el 27 de marzo de 2012

Lack of association between a functional genetic variant of connexin 37 and ischemic stroke in a Taiwanese population ⬇️

artículo científico publicado el 2 de febrero de 2012

Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke ⬇️

artículo científico publicado el 28 de enero de 2013

Lack of association between the IL-10 gene polymorphisms and features of the metabolic syndrome

artículo científico publicado el 1 de febrero de 2011

Let-7g improves multiple endothelial functions through targeting transforming growth factor-beta and SIRT-1 signaling

artículo científico publicado en 2013

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

artículo científico publicado en 2017

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

MicroRNA-195 regulates vascular smooth muscle cell phenotype and prevents neointimal formation ⬇️

artículo científico publicado el 16 de julio de 2012

MicroRNA-765 influences arterial stiffness through modulating apelin expression

artículo científico publicado en 2015

Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in Taiwan.

artículo científico publicado en 2019

Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese cohort with multiple cerebral cavernous malformations in Taiwan

artículo científico publicado en 2018

Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias

artículo científico publicado en 2017

Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis

artículo científico publicado en 2015

NOTCH3 cysteine-altering variant is an important risk factor for stroke in the Taiwanese population

scientific article published on 02 December 2019

Oxidized low-density lipoprotein is a common risk factor for cardiovascular diseases and gastroenterological cancers via epigenomical regulation of microRNA-210

artículo científico publicado en 2015

PDD-5S: A useful screening tool for Parkinson's disease dementia

artículo científico publicado en 2016

Plasma MCP-1 and Cognitive Decline in Patients with Alzheimer's Disease and Mild Cognitive Impairment: A Two-year Follow-up Study

artículo científico publicado en 2018

Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia

scientific article published on 10 December 2019

Plasma biomarkers are associated with agitation and regional brain atrophy in Alzheimer's disease

artículo científico publicado en 2017

Real-world evaluation of compliance and preference in Alzheimer's disease treatment: an observational study in Taiwan.

artículo científico publicado en 2016

Reply: A novel WARS mutation causes distal hereditary motor neuropathy in a Chinese family

scientific article published on 01 September 2019

SORL1 gene, plasma biomarkers, and the risk of Alzheimer's disease for the Han Chinese population in Taiwan

artículo científico publicado en 2016

Serum microRNA-21 and microRNA-221 as Potential Biomarkers for Cerebrovascular Disease ⬇️

artículo científico publicado el 13 de julio de 2013

Spinocerebellar ataxia type 36 in the Han Chinese

artículo científico publicado en 2016

Summative Effects of Vascular Risk Factors on the Progression of Alzheimer Disease

artículo científico publicado en 2019

The clinical significance of plasma clusterin and Aβ in the longitudinal follow-up of patients with Alzheimer's disease.

artículo científico publicado en 2017

Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease

artículo científico publicado en 2015

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia.

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2017

Lista de obras de

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

A novel DNAJB6 mutation causes dominantly inherited distal-onset myopathy and compromises DNAJB6 function

ABCA7 gene and the risk of Alzheimer's disease in Han Chinese in Taiwan

Characterization of Heterozygous HTRA1 Mutations in Taiwanese Patients With Cerebral Small Vessel Disease

Chromosome 9p21 Genetic Variants are Associated with Myocardial Infarction but Not with Ischemic Stroke in a Taiwanese Population ⬇️

Circulating microRNAs have a sex-specific association with metabolic syndrome

Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy.

Clinical and biophysical characterization of 19 GJB1 mutations.

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

Comparable progression of spinocerebellar ataxias between Caucasians and Chinese

Decreased MicroRNA-221 is Associated with High Levels of TNF-a in Human Adipose Tissue-Derived Mesenchymal Stem Cells From Obese Woman ⬇️

Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke

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

Elevated circulating endothelial-specific microRNAs in migraine patients: A pilot study.

Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan

Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant

Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis.

Investigating CYP2C19 loss-of-function allele statuses and their association with stroke of different etiologies in a Taiwanese population

Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia

Juvenile Huntington's disease presenting as difficult-to-treat seizure and the first episode of psychosis ⬇️

Lack of association between a functional genetic variant of connexin 37 and ischemic stroke in a Taiwanese population ⬇️

Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke ⬇️

Lack of association between the IL-10 gene polymorphisms and features of the metabolic syndrome

Let-7g improves multiple endothelial functions through targeting transforming growth factor-beta and SIRT-1 signaling

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

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

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

MicroRNA-195 regulates vascular smooth muscle cell phenotype and prevents neointimal formation ⬇️

MicroRNA-765 influences arterial stiffness through modulating apelin expression

Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in Taiwan.

Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese cohort with multiple cerebral cavernous malformations in Taiwan

Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias

Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis

NOTCH3 cysteine-altering variant is an important risk factor for stroke in the Taiwanese population

Oxidized low-density lipoprotein is a common risk factor for cardiovascular diseases and gastroenterological cancers via epigenomical regulation of microRNA-210

PDD-5S: A useful screening tool for Parkinson's disease dementia

Plasma MCP-1 and Cognitive Decline in Patients with Alzheimer's Disease and Mild Cognitive Impairment: A Two-year Follow-up Study

Plasma Transthyretin as a Predictor of Amnestic Mild Cognitive Impairment Conversion to Dementia

Plasma biomarkers are associated with agitation and regional brain atrophy in Alzheimer's disease

Real-world evaluation of compliance and preference in Alzheimer's disease treatment: an observational study in Taiwan.

Reply: A novel WARS mutation causes distal hereditary motor neuropathy in a Chinese family

SORL1 gene, plasma biomarkers, and the risk of Alzheimer's disease for the Han Chinese population in Taiwan

Serum microRNA-21 and microRNA-221 as Potential Biomarkers for Cerebrovascular Disease ⬇️

Spinocerebellar ataxia type 36 in the Han Chinese

Summative Effects of Vascular Risk Factors on the Progression of Alzheimer Disease

The clinical significance of plasma clusterin and Aβ in the longitudinal follow-up of patients with Alzheimer's disease.

Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia.

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

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