Dysregulated PIKfyve-dependent inhibition of ClC-7 causes ammonium-dependent endolysosomal vacuolization and autophagic flux impairment: Rescue by glutaminase inhibition

This publication has 60 references indexed in Scilit:

• An SLC12A9-dependent ion transport mechanism maintains lysosomal osmolarity
  Developmental Cell, 2024
• A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl−/H+-Exchanger, Causes Early-Onset Neurodegeneration
  The American Journal of Human Genetics, 2020
• PNU-120596, a positive allosteric modulator of α7 nicotinic acetylcholine receptor, directly inhibits p38 MAPK
  Biochemical Pharmacology, 2020
• Liver-Type Glutaminase GLS2 Is a Druggable Metabolic Node in Luminal-Subtype Breast Cancer
  Cell Reports, 2019
• Severe Consequences of SAC3/FIG4 Phosphatase Deficiency to Phosphoinositides in Patients with Charcot-Marie-Tooth Disease Type-4J
  Molecular Neurobiology, 2019
• Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification
  The American Journal of Human Genetics, 2019
• Disorders of lysosomal acidification—The emerging role of v-ATPase in aging and neurodegenerative disease
  Ageing Research Reviews, 2016
• Activation of muscarinic cholinoceptor ameliorates tumor necrosis factor‐α‐induced barrier dysfunction in intestinal epithelial cells
  FEBS Letters, 2015
• SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity
  Journal of Bone and Mineral Research, 2012
• Osmotic Regulation of Rab-Mediated Organelle Docking
  Current Biology, 2008