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Cadmium-induced apoptosis in primary rat cerebral cortical neurons culture is mediated by a calcium signaling pathway

PloS one, 2013-05, Vol.8 (5), p.e64330

2013

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ROS-Mediated Cell Cycle Arrest and Apoptosis Induced by Zearalenone in Mouse Sertoli Cells via ER Stress and the ATP/AMPK Pathway

Toxins, 2018-01, Vol.10 (1), p.24

2018

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Current concepts in the pathogenesis and treatment of chronic suppurative otitis media

Journal of medical microbiology, 2015-10, Vol.64 (10), p.1103-1116

2015

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The Effects of Autophagy and PI3K/AKT/m-TOR Signaling Pathway on the Cell-Cycle Arrest of Rats Primary Sertoli Cells Induced by Zearalenone

Toxins, 2018-09, Vol.10 (10), p.398

2018

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Tumor-Associated Macrophages in Vestibular Schwannoma and Relationship to Hearing

OTO open : the official open access journal of the American Academy of Otolaryngology--Head and Neck Surgery Foundation, 2021-10, Vol.5 (4), p.2473974X211059111-n/a

2021

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The genetic basis of deafness in populations of African descent

Journal of genetics and genomics, 2017-06, Vol.44 (6), p.285-294

2017

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Oxidative Stress and Apoptotic Changes of Rat Cerebral Cortical Neurons Exposed to Cadmium in Vitro

Biomedical and environmental sciences, 2012-04, Vol.25 (2), p.172-181

2012

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Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2–associated schwannomas reveals differences in efficacy and drug resistance development

Neuro-oncology (Charlottesville, Va.), 2019-03, Vol.21 (4), p.486-497

2019

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Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A

Stem cell research, 2022-01, Vol.58, p.102599-102599, Article 102599

2022

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Elucidation of repeat motifs R1‐ and R2‐related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals

Molecular genetics & genomic medicine, 2022-10, Vol.10 (10), p.e2015-n/a

2022

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Characterization of an induced pluripotent stem cell line (UMi040-A) bearing an auditory neuropathy spectrum disorder-associated variant in TMEM43

Stem cell research, 2022-05, Vol.61, p.102758-102758, Article 102758

2022

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PDZD7-MYO7A complex identified in enriched stereocilia membranes

eLife, 2016-08, Vol.5

2016

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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

Nature genetics, 2000-09, Vol.26 (1), p.51-55

2000

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Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss

Journal of human genetics, 2017-02, Vol.62 (2), p.317-320

2017

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Characterization of UMi028-A-1 stem cell line that contains a CRISPR/Cas9 induced hearing loss-associated variant (V60L (c.178G > T)) in the P2RX2 gene

Stem cell research, 2020-12, Vol.49, p.102017-102017, Article 102017

2020

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Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

Human genetics, 2009-02, Vol.125 (1), p.53-62

2009

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Neurotransmitters: The Critical Modulators Regulating Gut–Brain Axis

Journal of cellular physiology, 2017-09, Vol.232 (9), p.2359-2372

2017

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Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

Human molecular genetics, 2008-08, Vol.17 (15), p.2405-2415

2008

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Immunity Genes and Susceptibility to Otitis Media： A Comprehensive Review

Journal of genetics and genomics, 2014-11, Vol.41 (11), p.567-581

2014

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Effect of Cadmium on Rat Leydig Cell Testosterone Production and DNA Integrity in vitro

Biomedical and environmental sciences, 2013-09, Vol.26 (9), p.769-773

2013

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Cadmium-induced autophagy promotes survival of rat cerebral cortical neurons by activating class III phosphoinositide 3-kinase/beclin-1/B-cell lymphoma 2 signaling pathways

Molecular medicine reports, 2015-08, Vol.12 (2), p.2912-2918

2015

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Oxygen Saturation in Closed-Globe Blunt Ocular Trauma

BioMed research international, 2016-01, Vol.2016, p.8232468-5

2016

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Audioprofiles and antioxidant enzyme genotypes in presbycusis

The Laryngoscope, 2012-11, Vol.122 (11), p.2539-2542

2012

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Intricate Functions of Matrix Metalloproteinases in Physiological and Pathological Conditions

Journal of cellular physiology, 2016-12, Vol.231 (12), p.2599-2621

2016

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Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueduct

Otolaryngology-head and neck surgery, 2009-10, Vol.141 (4), p.502-508

2009

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Cadmium-induced apoptosis in primary rat cerebral cortical neurons culture is mediated by a calcium signaling pathway

ROS-Mediated Cell Cycle Arrest and Apoptosis Induced by Zearalenone in Mouse Sertoli Cells via ER Stress and the ATP/AMPK Pathway

Current concepts in the pathogenesis and treatment of chronic suppurative otitis media

The Effects of Autophagy and PI3K/AKT/m-TOR Signaling Pathway on the Cell-Cycle Arrest of Rats Primary Sertoli Cells Induced by Zearalenone

Tumor-Associated Macrophages in Vestibular Schwannoma and Relationship to Hearing

The genetic basis of deafness in populations of African descent

Oxidative Stress and Apoptotic Changes of Rat Cerebral Cortical Neurons Exposed to Cadmium in Vitro

Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2–associated schwannomas reveals differences in efficacy and drug resistance development

Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A

Elucidation of repeat motifs R1‐ and R2‐related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals

Characterization of an induced pluripotent stem cell line (UMi040-A) bearing an auditory neuropathy spectrum disorder-associated variant in TMEM43

PDZD7-MYO7A complex identified in enriched stereocilia membranes

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss

Characterization of UMi028-A-1 stem cell line that contains a CRISPR/Cas9 induced hearing loss-associated variant (V60L (c.178G > T)) in the P2RX2 gene

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

Neurotransmitters: The Critical Modulators Regulating Gut–Brain Axis

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

Immunity Genes and Susceptibility to Otitis Media： A Comprehensive Review

Effect of Cadmium on Rat Leydig Cell Testosterone Production and DNA Integrity in vitro

Cadmium-induced autophagy promotes survival of rat cerebral cortical neurons by activating class III phosphoinositide 3-kinase/beclin-1/B-cell lymphoma 2 signaling pathways

Oxygen Saturation in Closed-Globe Blunt Ocular Trauma

Audioprofiles and antioxidant enzyme genotypes in presbycusis

Intricate Functions of Matrix Metalloproteinases in Physiological and Pathological Conditions

Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueduct

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