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Kölliker’s organ-supporting cells and cochlear auditory development

Frontiers in molecular neuroscience, 2022-10, Vol.15, p.1031989-1031989

2022

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Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing

Frontiers in neurology, 2022-12, Vol.13, p.1026695-1026695

2022

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Pathological mechanisms of connexin26-related hearing loss: Potassium recycling, ATP-calcium signaling, or energy supply?

Frontiers in molecular neuroscience, 2022-09, Vol.15, p.976388-976388

2022

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Molecular etiology study of hearing loss in 13 Chinese Han families

Frontiers in neurology, 2022-11, Vol.13, p.1048218-1048218

2022

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Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca2+ Signaling in Kölliker’s Organ

Frontiers in cellular neuroscience, 2022-03, Vol.16, p.816079-816079

2022

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Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss

PloS one, 2015-05, Vol.10 (5), p.e0127879-e0127879

2015

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Pseudo-Temporal Analysis of Single-Cell RNA Sequencing Reveals Trans -Differentiation Potential of Greater Epithelial Ridge Cells Into Hair Cells During Postnatal Development of Cochlea in Rats

Frontiers in molecular neuroscience, 2022-03, Vol.15, p.832813-832813

2022

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Distinct Expression Patterns of Apoptosis and Autophagy-Associated Proteins and Genes during Postnatal Development of Spiral Ganglion Neurons in Rat

Neural plasticity, 2020-10, Vol.2020, p.1-9

2020

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Characterization of spectrum, de novo rate and genotype-phenotype correlation of dominant GJB2 mutations in Chinese hans

PloS one, 2014-06, Vol.9 (6), p.e100483-e100483

2014

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A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability

PloS one, 2015-03, Vol.10 (3), p.e0120816-e0120816

2015

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Mutation spectrum and differential gene expression in cystic and solid vestibular schwannoma

Genetics in medicine, 2014-03, Vol.16 (3), p.264-270

2014

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Single-Cell RNA Sequencing Analysis Reveals Greater Epithelial Ridge Cells Degeneration During Postnatal Development of Cochlea in Rats

Frontiers in cell and developmental biology, 2021-09, Vol.9, p.719491-719491

2021

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Molecular etiology of non-dominant, non-syndromic, mild-to-moderate childhood hearing impairment in Chinese Hans

American journal of medical genetics. Part A, 2014-12, Vol.164A (12), p.3115-3119

2014

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A liquid chromatography-mass spectroscopy-based untargeted metabolomic study of the rat cochlear nucleus at various stages of maturity

Hearing research, 2022-12, Vol.426, p.108645-108645, Article 108645

2022

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YTHDF1 Protects Auditory Hair Cells from Cisplatin-Induced Damage by Activating Autophagy via the Promotion of ATG14 Translation

Molecular neurobiology, 2022-12, Vol.59 (12), p.7134-7151

2022

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Molecular etiology and genotype-phenotype correlation of Chinese Han deaf patients with type I and type II Waardenburg Syndrome

Scientific reports, 2016-10, Vol.6 (1), p.35498-35498, Article 35498

2016

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Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencing

International journal of pediatric otorhinolaryngology, 2020-01, Vol.128, p.109689-109689, Article 109689

2020

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Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca 2+ Signaling in Kölliker's Organ

Frontiers in cellular neuroscience, 2022, Vol.16, p.816079

2022

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Potential biomarkers in peripheral blood mononuclear cells of patients with sporadic Ménière’s disease based on proteomics

Acta oto-laryngologica, 2023, Vol.143 (8), p.636-646

2023

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A Novel Missense Mutation of NOG Interferes With the Dimerization of NOG and Causes Proximal Symphalangism Syndrome in a Chinese Family

Annals of otology, rhinology & laryngology, 2015-09, Vol.124 (9), p.745-751

2015

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Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing loss

International journal of pediatric otorhinolaryngology, 2014-04, Vol.78 (4), p.614-617

2014

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Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing loss

International journal of pediatric otorhinolaryngology, 2015-10, Vol.79 (10), p.1654-1657

2015

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A 1.6-Mb Microdeletion in Chromosome 17q22 Leads to NOG-Related Symphalangism Spectrum Disorder without Intellectual Disability: e0120816

PloS one, 2015-03, Vol.10 (3)

2015

Volltextzugriff (PDF)

Microbial Energy Conversion

Yuan, Zhenhong

1st edition., 2018

Volltextzugriff (PDF)

The roles of Mesp family proteins： functional diversity and redundancy in differentiation of pluripotent stem cells and mammalian mesodermal development

Protein & cell, 2015-08, Vol.6 (8), p.553-561

2015

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Kölliker’s organ-supporting cells and cochlear auditory development

Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing

Pathological mechanisms of connexin26-related hearing loss: Potassium recycling, ATP-calcium signaling, or energy supply?

Molecular etiology study of hearing loss in 13 Chinese Han families

Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca2+ Signaling in Kölliker’s Organ

Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss

Pseudo-Temporal Analysis of Single-Cell RNA Sequencing Reveals Trans -Differentiation Potential of Greater Epithelial Ridge Cells Into Hair Cells During Postnatal Development of Cochlea in Rats

Distinct Expression Patterns of Apoptosis and Autophagy-Associated Proteins and Genes during Postnatal Development of Spiral Ganglion Neurons in Rat

Characterization of spectrum, de novo rate and genotype-phenotype correlation of dominant GJB2 mutations in Chinese hans

A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability

Mutation spectrum and differential gene expression in cystic and solid vestibular schwannoma

Single-Cell RNA Sequencing Analysis Reveals Greater Epithelial Ridge Cells Degeneration During Postnatal Development of Cochlea in Rats

Molecular etiology of non-dominant, non-syndromic, mild-to-moderate childhood hearing impairment in Chinese Hans

A liquid chromatography-mass spectroscopy-based untargeted metabolomic study of the rat cochlear nucleus at various stages of maturity

YTHDF1 Protects Auditory Hair Cells from Cisplatin-Induced Damage by Activating Autophagy via the Promotion of ATG14 Translation

Molecular etiology and genotype-phenotype correlation of Chinese Han deaf patients with type I and type II Waardenburg Syndrome

Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencing

Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca 2+ Signaling in Kölliker's Organ

Potential biomarkers in peripheral blood mononuclear cells of patients with sporadic Ménière’s disease based on proteomics

A Novel Missense Mutation of NOG Interferes With the Dimerization of NOG and Causes Proximal Symphalangism Syndrome in a Chinese Family

Identification of both MT-RNR1 m.1555A>G and bi-allelic GJB2 mutations in probands with non-syndromic hearing loss

Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing loss

A 1.6-Mb Microdeletion in Chromosome 17q22 Leads to NOG-Related Symphalangism Spectrum Disorder without Intellectual Disability: e0120816

Microbial Energy Conversion

The roles of Mesp family proteins： functional diversity and redundancy in differentiation of pluripotent stem cells and mammalian mesodermal development

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