Results 31 to 40 of about 29,691,692 (162)

The RA11 and RA12 antibodies recognize a peptide of the D. discoideum Mucolipin protein by western blot

open access: yes, 2020
The recombinant antibodies RA11 and RA12 detect by western blot a peptide of the Dictyostelium discoideum Mucolipin protein fused to a GST ...
Blanc, Cédric, Zufferey, Madeleine
core   +2 more sources

TRPML1 as a potential therapeutic target for triple-negative breast cancer: a review

open access: yesFrontiers in Oncology, 2023
Triple-negative breast cancer (TNBC) is the most refractory subtype of breast cancer, and effective treatments are urgently needed owing to its poor prognosis.
Ying Pan   +6 more
doaj   +1 more source

Identification of the Penta-EF-hand Protein ALG-2 as a Ca2+-dependent Interactor of Mucolipin-1 [PDF]

open access: yesJournal of Biological Chemistry, 2009
Loss of function mutations in mucolipin-1 (MCOLN1) have been linked to mucolipidosis type IV (MLIV), a recessive lysosomal storage disease characterized by severe neurological and ophthalmological abnormalities. MCOLN1 is an ion channel that regulates membrane transport along the endolysosomal pathway.
Silvia, Vergarajauregui   +2 more
openaire   +2 more sources

miR-204 silencing reduces mitochondrial autophagy and ROS production in a murine AD model via the TRPML1-activated STAT3 pathway

open access: yesMolecular Therapy: Nucleic Acids, 2021
Mitochondrial dysfunction is an early feature of Alzheimer’s disease (AD), whereby accumulation of damaged mitochondria in conjunction with impaired mitophagy contributes to neurodegeneration.
Lu Zhang   +7 more
doaj   +1 more source

Structural basis for PtdInsP2-mediated human TRPML1 regulation

open access: yesNature Communications, 2018
Transient receptor potential mucolipin 1 (TRPML1) is a lysosomal channel which maintains the low pH and calcium levels for lysosomal function. Here authors use structural biology and electrophysiology to show how lipids bind and allosterically activate ...
Michael Fine   +2 more
doaj   +1 more source

Abnormal Lysosomal Positioning and Small Extracellular Vesicle Secretion in Arterial Stiffening and Calcification of Mice Lacking Mucolipin 1 Gene [PDF]

open access: yesInternational Journal of Molecular Sciences, 2020
Recent studies have shown that arterial medial calcification is mediated by abnormal release of exosomes/small extracellular vesicles from vascular smooth muscle cells (VSMCs) and that small extracellular vesicle (sEV) secretion from cells is associated with lysosome activity.
Bhat, Owais M.   +4 more
openaire   +2 more sources

Induction of lysosomal exocytosis and biogenesis via TRPML1 activation for the treatment of uranium-induced nephrotoxicity

open access: yesNature Communications, 2023
Uranium (U) is a well-known nephrotoxicant which forms precipitates in the lysosomes of renal proximal tubular epithelial cells (PTECs) after U-exposure at a cytotoxic dose.
Dengqin Zhong   +5 more
doaj   +1 more source

Transcriptome dataset of light-dependent expression in the early onset retinal degeneration model, Mcoln1−/− mouse

open access: yesData in Brief, 2023
Retinal degenerative diseases (RDDs) are a diverse group of retinal disorders that cause visual impairment. While RDD prevalence is high, little is known about the molecular mechanisms underlying the pathogenesis within many of these disorders.
Rebecca Cistulli   +3 more
doaj   +1 more source

Endo-lysosomal TRP mucolipin-1 channels trigger global ER Ca2+ release and Ca2+ influx [PDF]

open access: yesJournal of Cell Science, 2016
ABSTRACT Transient receptor potential (TRP) mucolipins (TRPMLs), encoded by the MCOLN genes, are patho-physiologically relevant endo-lysosomal ion channels crucial for membrane trafficking. Several lines of evidence suggest that TRPMLs mediate localised Ca2+ release but their role in Ca2+ signalling is not clear.
Bethan S. Kilpatrick   +4 more
openaire   +3 more sources

Caenorhabditis elegans functional orthologue of human protein h-mucolipin-1 is required for lysosome biogenesis [PDF]

open access: yesProceedings of the National Academy of Sciences, 2004
Mucolipidosis type IV (MLIV) is an autosomal recessive lysosomal storage disease characterized by severe psychomotor retardation, achlorhydria, and ophthalmological abnormalities. Cells from several tissues in MLIV patients accumulate large vacuoles that are presumed to be lysosomes, but whose exact nature remains to be determined.
Sebastian, Treusch   +5 more
openaire   +2 more sources

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