Solute carrier family 4 member 1 might participate in the pathogenesis of Meniere's disease in a murine endolymphatic hydrop model
Author:
Affiliation:
1. Department of Otolaryngology-Head and Neck Surgery, Shandong Provincial ENT Hospital Affiliated to Shandong University, Jinan 250022, P.R. China
Publisher
Informa UK Limited
Subject
Otorhinolaryngology,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/00016489.2019.1663365
Reference20 articles.
1. Prevalence of Menière's Disease in General Population of Southern Finland
2. RNA-sequencing study of peripheral blood mononuclear cells in sporadic Ménière's disease patients: possible contribution of immunologic dysfunction to the development of this disorder
3. Early Hearing Loss upon Disruption of Slc4a10 in C57BL/6 Mice
4. Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context
5. Mis-trafficking of bicarbonate transporters: implications to human diseasesThis paper is one of a selection of papers published in a Special Issue entitled CSBMCB 53rd Annual Meeting — Membrane Proteins in Health and Disease, and has undergone the Journal’s usual peer review process.
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1. Potential Theranostic Roles of SLC4 Molecules in Human Diseases;International Journal of Molecular Sciences;2023-10-13
2. New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s Disease;Genes;2022-06-01
3. Characterization of the microRNA transcriptomes and proteomics of cochlear tissue-derived small extracellular vesicles from mice of different ages after birth;Cellular and Molecular Life Sciences;2022-02-26
4. Planar Cell Polarity Defects and Hearing Loss in Sperm-Associated Antigen 6 (Spag6)-Deficient Mice;American Journal of Physiology-Cell Physiology;2020-11-11
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