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Ototoxicity among cisplatin, carboplatin, and oxaliplatin in zebrafish model

Environmental toxicology, 2024-07, Vol.39 (7), p.4058-4065

2024

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Protective mechanism of ferulic acid against neomycin‐induced ototoxicity in zebrafish

Environmental toxicology, 2023-03, Vol.38 (3), p.604-614

2023

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Cichoric Acid May Play a Role in Protecting Hair Cells from Ototoxic Drugs

International journal of molecular sciences, 2022-06, Vol.23 (12), p.6701

2022

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3-Bromofluoranthene-induced cardiotoxicity of zebrafish and apoptosis in the vascular endothelial cells via intrinsic and extrinsic caspase-dependent pathways

Ecotoxicology and environmental safety, 2021-12, Vol.228, p.112962, Article 112962

2021

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Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomes

Scientific reports, 2020-08, Vol.10 (1), p.13375, Article 13375

2020

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Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss

International journal of molecular sciences, 2020-03, Vol.21 (7), p.2382

2020

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Early Blood Glucose Level Post-Admission Correlates with the Outcomes and Oxidative Stress in Neonatal Hypoxic-Ischemic Encephalopathy

Antioxidants, 2021-12, Vol.11 (1), p.39

2021

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Parapyruvate Induces Neurodegeneration in C57BL/6JNarl Mice via Inhibition of the α‑Ketoglutarate Dehydrogenase Complex

ACS omega, 2024-02, Vol.9 (5), p.5919-5931

2024

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A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study

Journal of personalized medicine, 2020-12, Vol.10 (4), p.281

2020

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Evaluation of nephrotoxic effects of mycotoxins, citrinin and patulin, on zebrafish (Danio rerio) embryos

Food and chemical toxicology, 2012-12, Vol.50 (12), p.4398-4404

2012

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A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan

Journal of the Formosan Medical Association, 2017-09, Vol.116 (9), p.711-719

2017

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KCNQ2 Selectivity Filter Mutations Cause Kv7.2 M-Current Dysfunction and Configuration Changes Manifesting as Epileptic Encephalopathies and Autistic Spectrum Disorders

Cells (Basel, Switzerland), 2022-03, Vol.11 (5), p.894

2022

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Rutin decreases lipopolysaccharide-induced acute lung injury via inhibition of oxidative stress and the MAPK-NF-κB pathway

Free radical biology & medicine, 2014-04, Vol.69, p.249-257

2014

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KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization

Epilepsy & behavior, 2024-07, Vol.156, p.109798, Article 109798

2024

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Aflatoxin B1 interferes with embryonic liver development: Involvement of p53 signaling and apoptosis in zebrafish

Toxicology (Amsterdam), 2021-06, Vol.458, p.152844-152844, Article 152844

2021

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Mechanism of a novel missense mutation, p.V174M, of the human connexin31 (GJB3) in causing nonsyndromic hearing loss

Biochemistry and cell biology, 2014-08, Vol.92 (4), p.251

2014

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Ovatodiolide Inhibits Breast Cancer Stem/Progenitor Cells through SMURF2-Mediated Downregulation of Hsp27

Toxins, 2016-04, Vol.8 (5), p.127-127

2016

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The Functional Role of CONNEXIN 26 Mutation in Nonsyndromic Hearing Loss, Demonstrated by Zebrafish Connexin 30.3 Homologue Model

Cells (Basel, Switzerland), 2020-05, Vol.9 (5), p.1291

2020

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Ferulic acid-mediated protection against neomycin-induced hair cell loss in transgenic zebrafish

Journal of functional foods, 2017-01, Vol.28, p.157-167

2017

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Androgen excess down-regulates connexin43 in a human granulosa cell line

Fertility and sterility, 2010-12, Vol.94 (7), p.2938-2941

2010

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Advances and Applications of Ion Torrent Personal Genome Machine in Cutaneous Squamous Cell Carcinoma Reveal Novel Gene Mutations

Materials, 2016-06, Vol.9 (6), p.464

2016

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Lenticulostriate Vasculopathy in Brain Ultrasonography is Associated with Cytomegalovirus Infection in Newborns

Pediatrics and neonatology, 2015-12, Vol.56 (6), p.408-414

2015

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A novel missense mutation in the connexin30 causes nonsyndromic hearing loss

PloS one, 2011-06, Vol.6 (6), p.e21473-e21473

2011

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Vascular endothelial dysfunction induced by 3-bromofluoranthene via MAPK-mediated-NFκB pro-inflammatory pathway and intracellular ROS generation

Archives of toxicology, 2024-07, Vol.98 (7), p.2247-2259

2024

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Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30

European journal of human genetics : EJHG, 2010-09, Vol.18 (9), p.1061-1064

2010

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Ototoxicity among cisplatin, carboplatin, and oxaliplatin in zebrafish model

Protective mechanism of ferulic acid against neomycin‐induced ototoxicity in zebrafish

Cichoric Acid May Play a Role in Protecting Hair Cells from Ototoxic Drugs

3-Bromofluoranthene-induced cardiotoxicity of zebrafish and apoptosis in the vascular endothelial cells via intrinsic and extrinsic caspase-dependent pathways

Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomes

Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss

Early Blood Glucose Level Post-Admission Correlates with the Outcomes and Oxidative Stress in Neonatal Hypoxic-Ischemic Encephalopathy

Parapyruvate Induces Neurodegeneration in C57BL/6JNarl Mice via Inhibition of the α‑Ketoglutarate Dehydrogenase Complex

A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study

Evaluation of nephrotoxic effects of mycotoxins, citrinin and patulin, on zebrafish (Danio rerio) embryos

A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan

KCNQ2 Selectivity Filter Mutations Cause Kv7.2 M-Current Dysfunction and Configuration Changes Manifesting as Epileptic Encephalopathies and Autistic Spectrum Disorders

Rutin decreases lipopolysaccharide-induced acute lung injury via inhibition of oxidative stress and the MAPK-NF-κB pathway

KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization

Aflatoxin B1 interferes with embryonic liver development: Involvement of p53 signaling and apoptosis in zebrafish

Mechanism of a novel missense mutation, p.V174M, of the human connexin31 (GJB3) in causing nonsyndromic hearing loss

Ovatodiolide Inhibits Breast Cancer Stem/Progenitor Cells through SMURF2-Mediated Downregulation of Hsp27

The Functional Role of CONNEXIN 26 Mutation in Nonsyndromic Hearing Loss, Demonstrated by Zebrafish Connexin 30.3 Homologue Model

Ferulic acid-mediated protection against neomycin-induced hair cell loss in transgenic zebrafish

Androgen excess down-regulates connexin43 in a human granulosa cell line

Advances and Applications of Ion Torrent Personal Genome Machine in Cutaneous Squamous Cell Carcinoma Reveal Novel Gene Mutations

Lenticulostriate Vasculopathy in Brain Ultrasonography is Associated with Cytomegalovirus Infection in Newborns

A novel missense mutation in the connexin30 causes nonsyndromic hearing loss

Vascular endothelial dysfunction induced by 3-bromofluoranthene via MAPK-mediated-NFκB pro-inflammatory pathway and intracellular ROS generation

Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30

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