Engineered Pendrin Protein, an Anion Transporter and Molecular Motor
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference44 articles.
1. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
2. Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes
3. Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification
4. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4
5. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
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1. Single particle cryo-EM structure of the outer hair cell motor protein prestin;Nature Communications;2022-01-12
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3. Low-Intensity Ultrasound Causes Direct Excitation of Auditory Cortical Neurons;Neural Plasticity;2021-04-04
4. The extracellular loop of pendrin and prestin modulates their voltage-sensing property;Journal of Biological Chemistry;2018-06
5. Auditory Brainstem Response and Outer Hair Cell Whole-cell Patch Clamp Recording in Postnatal Rats;Journal of Visualized Experiments;2018-05-24
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