A conserved function of Pkhd1l1, a mammalian hair cell stereociliary coat protein, in regulating hearing in zebrafish-Reference-Cited by-同舟云学术

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A conserved function of Pkhd1l1, a mammalian hair cell stereociliary coat protein, in regulating hearing in zebrafish

Published:2023-03-24 Issue:3 Volume:37 Page:85-92
ISSN:0167-7063
Container-title:Journal of Neurogenetics
language:en
Short-container-title:Journal of Neurogenetics

Author:

Makrogkikas Stylianos¹²,Cheng Ruey-Kuang¹,Lu Hao¹,Roy Sudipto¹²³^ORCID

Affiliation:

1. Institute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore

2. Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore

3. Department of Biological Sciences, National University of Singapore, Singapore, Singapore

Funder

Singapore International Graduate Award

Agency for Science, Technology and Research (A*STAR) of Singapore

Publisher

Informa UK Limited

Subject

Cellular and Molecular Neuroscience,Genetics

Link

https://www.tandfonline.com/doi/pdf/10.1080/01677063.2023.2187792

Reference21 articles.

1. Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss

2. RNA-seq transcriptomic analysis of adult zebrafish inner ear hair cells

3. The habenula clock influences response to a stressor

4. Characterization of the Transcriptome of Nascent Hair Cells and Identification of Direct Targets of the Atoh1 Transcription Factor

5. Diagnosis and Treatment of Congenital Sensorineural Hearing Loss

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. PKHD1L1 is required for stereocilia bundle maintenance, durable hearing function and resilience to noise exposure;2024-03-04

2. PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss;Human Genetics;2024-03

3. PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss;2023-10-09

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