Found: 21
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Ototoxicity among cisplatin, carboplatin, and oxaliplatin in zebrafish model.
- Published in:
- Environmental Toxicology, 2024, v. 39, n. 7, p. 4058, doi. 10.1002/tox.24285
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- Publication type:
- Article
Protective mechanism of ferulic acid against neomycin‐induced ototoxicity in zebrafish.
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- Environmental Toxicology, 2023, v. 38, n. 3, p. 604, doi. 10.1002/tox.23707
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- Publication type:
- Article
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.
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- Journal of Personalized Medicine, 2020, v. 10, n. 4, p. 281, doi. 10.3390/jpm10040281
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- Article
KCNQ2-Associated Neonatal Epilepsy: Phenotype Might Correlate With Genotype.
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- Journal of Child Neurology, 2017, v. 32, n. 8, p. 704, doi. 10.1177/0883073817701873
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- Publication type:
- Article
Cichoric Acid May Play a Role in Protecting Hair Cells from Ototoxic Drugs.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 12, p. 6701, doi. 10.3390/ijms23126701
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- Publication type:
- Article
Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 7, p. 2382, doi. 10.3390/ijms21072382
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- Publication type:
- Article
Vascular endothelial dysfunction induced by 3-bromofluoranthene via MAPK-mediated-NFκB pro-inflammatory pathway and intracellular ROS generation.
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- Archives of Toxicology, 2024, v. 98, n. 7, p. 2247, doi. 10.1007/s00204-024-03751-0
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- Publication type:
- Article
Mechanism of Two Novel Human GJC3 Missense Mutations in Causing Non-Syndromic Hearing Loss.
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- Cell Biochemistry & Biophysics, 2013, v. 66, n. 2, p. 277, doi. 10.1007/s12013-012-9481-8
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- Publication type:
- Article
Human Connexin30.2/31.3 (GJC3) does not Form Functional Gap Junction Channels but Causes Enhanced ATP Release in HeLa Cells.
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- Cell Biochemistry & Biophysics, 2011, v. 61, n. 1, p. 189, doi. 10.1007/s12013-011-9188-2
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- Article
Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.
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- 2007
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- Publication type:
- journal article
Identification of Novel Mutations in the KCNQ4 Gene of Patients with Nonsyndromic Deafness from Taiwan.
- Published in:
- Audiology & Neurotology, 2007, v. 12, n. 1, p. 20, doi. 10.1159/000096154
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- Publication type:
- Article
Effects of Human Parvovirus B19 and Bocavirus VP1 Unique Region on Tight Junction of Human Airway Epithelial A549 Cells.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107970
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- Publication type:
- Article
Transglutaminase 2 Contributes to Apoptosis Induction in Jurkat T Cells by Modulating Ca<sup>2+</sup> Homeostasis via Cross-Linking RAP1GDS1.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0081516
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- Publication type:
- Article
Erratum to: Novel mutations in the connexin43 ( GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss.
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- 2010
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- Publication type:
- Correction Notice
Mycotoxin ochratoxin A disrupts renal development via a miR-731/prolactin receptor axis in zebrafish.
- Published in:
- Toxicology Research, 2016, v. 5, n. 2, p. 519, doi. 10.1039/c5tx00360a
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- Publication type:
- Article
Early Blood Glucose Level Post-Admission Correlates with the Outcomes and Oxidative Stress in Neonatal Hypoxic-Ischemic Encephalopathy.
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- Antioxidants, 2022, v. 11, n. 1, p. 39, doi. 10.3390/antiox11010039
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- Publication type:
- Article
Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomes.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70212-w
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- Publication type:
- Article
KCNQ2 Selectivity Filter Mutations Cause Kv7.2 M-Current Dysfunction and Configuration Changes Manifesting as Epileptic Encephalopathies and Autistic Spectrum Disorders.
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- Cells (2073-4409), 2022, v. 11, n. 5, p. 894, doi. 10.3390/cells11050894
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- Publication type:
- Article
The Functional Role of CONNEXIN 26 Mutation in Nonsyndromic Hearing Loss, Demonstrated by Zebrafish Connexin 30.3 Homologue Model.
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- Cells (2073-4409), 2020, v. 9, n. 5, p. 1291, doi. 10.3390/cells9051291
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- Publication type:
- Article
Cardiotoxicity of Mycotoxin Citrinin and Involvement of MicroRNA-138 in Zebrafish Embryos.
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- Toxicological Sciences, 2013, v. 136, n. 2, p. 402, doi. 10.1093/toxsci/kft206
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- Publication type:
- Article
Mechanism of a novel missense mutation, p.V174M, of the human connexin31 ( GJB3) in causing nonsyndromic hearing loss.
- Published in:
- Biochemistry & Cell Biology, 2014, v. 92, n. 4, p. 251, doi. 10.1139/bcb-2013-0126
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- Publication type:
- Article