about
Loss of PINK1 function promotes mitophagy through effects on oxidative stress and mitochondrial fissionAutophagy in lysosomal storage disordersThe cell biology of disease: lysosomal storage disorders: the cellular impact of lysosomal dysfunctionClarifying lysosomal storage diseasesNeurologic, gastric, and opthalmologic pathologies in a murine model of mucolipidosis type IVThe role of TRPMLs in endolysosomal trafficking and functionAfter the banquet: mitochondrial biogenesis, mitophagy, and cell survivalDefective Autophagy, Mitochondrial Clearance and Lipophagy in Niemann-Pick Type B LymphocytesATP13A2 regulates mitochondrial bioenergetics through macroautophagyMucolipidosis type IV: an updateA block of autophagy in lysosomal storage disordersSystematic screens for proteins that interact with the mucolipidosis type IV protein TRPML1Macroautophagy is defective in mucolipin-1-deficient mouse neuronsReduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1Mitochondria and quality control defects in a mouse model of Gaucher disease--links to Parkinson's diseaseMitotic slippage in non-cancer cells induced by a microtubule disruptor, disorazole C1.Aberrant Ca2+ handling in lysosomal storage disordersMucolipins: Intracellular TRPML1-3 channelsCommon and uncommon pathogenic cascades in lysosomal storage diseasesZinc dyshomeostasis is linked with the loss of mucolipidosis IV-associated TRPML1 ion channel.Neuropathology of the Mcoln1(-/-) knockout mouse model of mucolipidosis type IV.A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletionsDiversity in the regulation of autophagy and mitophagy: lessons from Parkinson's disease.TRPML: transporters of metals in lysosomes essential for cell survival?Defects in calcium homeostasis and mitochondria can be reversed in Pompe disease.Loss of lysosomal ion channel transient receptor potential channel mucolipin-1 (TRPML1) leads to cathepsin B-dependent apoptosis.Role of TRP channels in the regulation of the endosomal pathway.Pompe disease: Shared and unshared features of lysosomal storage disordersThe mucolipin-2 (TRPML2) ion channel: a tissue-specific protein crucial to normal cell function.Eaten alive: autophagy and neuronal cell death after hypoxia-ischemia.Different molecular mechanisms involved in spontaneous and oxidative stress-induced mitochondrial fragmentation in tripeptidyl peptidase-1 (TPP-1)-deficient fibroblasts.Membrane traffic and turnover in TRP-ML1-deficient cells: a revised model for mucolipidosis type IV pathogenesisLysosomal Storage Diseases-Regulating Neurodegeneration.Autophagic dysfunction in mucolipidosis type IV patients.Autophagy in neuroprotection and neurodegeneration: A question of balance.Monitoring mitophagy in neuronal cell cultures.Mitochondrially localized ERK2 regulates mitophagy and autophagic cell stress: implications for Parkinson's disease.Membrane trafficking in neuronal maintenance and degeneration.Mucolipidosis type IV: the importance of functional lysosomes for efficient autophagyMitochondrial Ca2+ homeostasis in lysosomal storage diseases.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Mitochondrial aberrations in mucolipidosis Type IV.
@en
Mitochondrial aberrations in mucolipidosis Type IV.
@nl
type
label
Mitochondrial aberrations in mucolipidosis Type IV.
@en
Mitochondrial aberrations in mucolipidosis Type IV.
@nl
prefLabel
Mitochondrial aberrations in mucolipidosis Type IV.
@en
Mitochondrial aberrations in mucolipidosis Type IV.
@nl
P2093
P2860
P356
P1476
Mitochondrial aberrations in mucolipidosis Type IV.
@en
P2093
Jian-Hui Zhu
John J Jennings
Kirill Kiselyov
Youssef Rbaibi
P2860
P304
39041-39050
P356
10.1074/JBC.M607982200
P407
P577
2006-10-20T00:00:00Z