Genetic Diseases of PIEZO1 and PIEZO2 Dysfunction
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Publisher
Elsevier
Reference121 articles.
1. Plug-N-Play: Mechanotransduction goes modular;Akyuz;Neuron,2016
2. Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay;Al-Sayed;American Journal of Human Genetics,2013
3. Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels;Albuisson;Nature Communications,2013
4. Screening for mutations in PIEZO2 that cause Distal Arthrogryposis Type 5;Almanza,2014
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1. The Piezo channel is a mechano-sensitive complex component in the mammalian inner ear hair cell;Nature Communications;2024-01-16
2. Transmembrane protein 120A (TMEM-120A/TACAN) coordinates with PIEZO channel during Caenorhabditis elegans reproductive regulation;G3: Genes, Genomes, Genetics;2023-12-05
3. Good vibrations;Science;2023-08-25
4. Piezo1 in Digestive System Function and Dysfunction;International Journal of Molecular Sciences;2023-08-19
5. Mutation in F-actin Polymerization Factor Suppresses Distal Arthrogryposis Type 5 (DA5) PIEZO2 Pathogenic Variant inCaenorhabditis elegans;2023-07-24
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