Detalhe da pesquisa
1.
KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization.
Epilepsy Behav
; 156: 109798, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38788659
2.
Vascular endothelial dysfunction induced by 3-bromofluoranthene via MAPK-mediated-NFκB pro-inflammatory pathway and intracellular ROS generation.
Arch Toxicol
; 98(7): 2247-2259, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38635053
3.
Ototoxicity among cisplatin, carboplatin, and oxaliplatin in zebrafish model.
Environ Toxicol
; 39(7): 4058-4065, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38661261
4.
Protective mechanism of ferulic acid against neomycin-induced ototoxicity in zebrafish.
Environ Toxicol
; 38(3): 604-614, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36367326
5.
Cichoric Acid May Play a Role in Protecting Hair Cells from Ototoxic Drugs.
Int J Mol Sci
; 23(12)2022 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35743144
6.
3-Bromofluoranthene-induced cardiotoxicity of zebrafish and apoptosis in the vascular endothelial cells via intrinsic and extrinsic caspase-dependent pathways.
Ecotoxicol Environ Saf
; 228: 112962, 2021 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34775346
7.
Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss.
Int J Mol Sci
; 21(7)2020 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32235586
8.
An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma.
Int J Med Sci
; 14(12): 1251-1256, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29104481
9.
Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene.
Int J Med Sci
; 14(3): 246-256, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28367085
10.
A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan.
J Formos Med Assoc
; 116(9): 711-719, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28038823
11.
Mechanism of a novel missense mutation, p.V174M, of the human connexin31 (GJB3) in causing nonsyndromic hearing loss.
Biochem Cell Biol
; 92(4): 251-7, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24913888
12.
Parapyruvate Induces Neurodegeneration in C57BL/6JNarl Mice via Inhibition of the α-Ketoglutarate Dehydrogenase Complex.
ACS Omega
; 9(5): 5919-5931, 2024 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38343944
13.
KCNQ2 Selectivity Filter Mutations Cause Kv7.2 M-Current Dysfunction and Configuration Changes Manifesting as Epileptic Encephalopathies and Autistic Spectrum Disorders.
Cells
; 11(5)2022 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35269516
14.
Early Blood Glucose Level Post-Admission Correlates with the Outcomes and Oxidative Stress in Neonatal Hypoxic-Ischemic Encephalopathy.
Antioxidants (Basel)
; 11(1)2021 Dec 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35052543
15.
Aflatoxin B1 interferes with embryonic liver development: Involvement of p53 signaling and apoptosis in zebrafish.
Toxicology
; 458: 152844, 2021 06 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34214637
16.
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss.
Hum Genet
; 127(2): 191-9, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19876648
17.
Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss.
Hum Genet
; 127(5): 545-51, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20130915
18.
Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.
Hum Genet
; 128(3): 303-13, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20593197
19.
Identification of novel variants in the Cx29 gene of nonsyndromic hearing loss patients using buccal cells and restriction fragment length polymorphism method.
Audiol Neurootol
; 15(2): 81-7, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-19657183
20.
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.
J Pers Med
; 10(4)2020 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33333793