Gain-of-function Mutation in TRPML3 Causes the Mouse Varitint-Waddler Phenotype
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference9 articles.
1. TRP channels: An overview
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3. TRPpathies
4. Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice
5. TRPML3 and hearing loss in the varitint-waddler mouse
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2. TRPML1 gating modulation by allosteric mutations and lipids (Design of allosteric mutations that recapitulate the gating of TRPML1);2024-08-23
3. TRPML1 gating modulation by allosteric mutations and lipids (Design of allosteric mutations that recapitulate the gating of TRPML1);2024-07-07
4. TRPML3/BK complex promotes autophagy and bacterial clearance by providing a positive feedback regulation of mTOR via PI3P;Proceedings of the National Academy of Sciences;2023-08-16
5. Gene expression of TRPMLs and its regulation by pathogen stimulation;Gene;2023-05
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