Opening the TRPML Gates
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry
Reference13 articles.
1. Identification of the gene causing mucolipidosis type IV
2. Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice
3. A helix-breaking mutation in TRPML3 leads to constitutive activity underlying deafness in the varitint-waddler mouse
4. Small Molecule Activators of TRPML3
5. Gain-of-function Mutation in TRPML3 Causes the Mouse Varitint-Waddler Phenotype
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1. (S)‐ML‐SA1 Activates Autophagy via TRPML1‐TFEB Pathway;ChemBioChem;2024-08-12
2. A novel BRET-based assay to investigate binding and residence time of unmodified ligands to the human lysosomal ion channel TRPML1 in intact cells;Journal of Biological Chemistry;2023-06
3. Expanding the Toolbox: Novel Modulators of Endolysosomal Cation Channels;Handbook of Experimental Pharmacology;2022
4. TRP Channels as Interior Designers: Remodeling the Endolysosomal Compartment in Natural Killer Cells;Frontiers in Immunology;2020-04-28
5. An overview on transient receptor potential channels superfamily;Behavioural Pharmacology;2019-12-10
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