Normal lysosomal morphology and function in LAMP-1-deficient mice - Test2 - elhamkhani - TriplyDB

Normal lysosomal morphology and function in LAMP-1-deficient mice

Normal lysosomal morphology and function in LAMP-1-deficient mice

http://www.wikidata.org/entity/Q28142071

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Virus entry. Lassa virus entry requires a trigger-induced receptor switch LAMP1/CD107a is required for efficient perforin delivery to lytic granules and NK-cell cytotoxicity Role of adaptor complex AP-3 in targeting wild-type and mutated CD63 to lysosomes VAMP7 regulates constitutive membrane incorporation of the cold-activated channel TRPM8.SLC26A Gene Family Participate in pH Regulation during Enamel Maturation Crystal structure of the conserved domain of the DC lysosomal associated membrane protein: implications for the lysosomal glycocalyx Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissue Syntaxin 7 mediates endocytic trafficking to late endosomes LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice Expression of the lysosomal-associated membrane protein-1 (LAMP-1) in astrocytomas Impaired glucose tolerance in a mouse model of sidt2 deficiency Specific Endocytosis Blockade of Trypanosoma cruzi Exposed to a Poly-LAcNAc Binding Lectin Suggests that Lectin-Sugar Interactions Participate to Receptor-Mediated Endocytosis Identification of Putative Receptors for the Novel Adipokine CTRP3 Using Ligand-Receptor Capture Technology Role of LAMP-2 in lysosome biogenesis and autophagy Neuraminidase 1 is a negative regulator of lysosomal exocytosis Expression and vesicular localization of mouse Trpml3 in stria vascularis, hair cells, and vomeronasal and olfactory receptor neurons "Late" macroendosomes and acidic endosomes in vertebrate motor nerve terminals.Effects of lysosomal membrane protein depletion on the Salmonella-containing vacuole.Impact of chronic alcohol ingestion on cardiac muscle protein expression The mTOR kinase inhibitor Everolimus decreases S6 kinase phosphorylation but fails to reduce mutant huntingtin levels in brain and is not neuroprotective in the R6/2 mouse model of Huntington's disease.Signals from the lysosome: a control centre for cellular clearance and energy metabolism.Endolysosomal proteolysis and its regulation.Impaired autophagosome clearance contributes to cardiomyocyte death in ischemia/reperfusion injury.Autophagy-mediated clearance of huntingtin aggregates triggered by the insulin-signaling pathway.LAMP-2 absence interferes with plasma membrane repair and decreases T. cruzi host cell invasion Adaptor protein complex 2-mediated, clathrin-dependent endocytosis, and related gene activities, are a prominent feature during maturation stage amelogenesis Role of TSPAN9 in Alphavirus Entry and Early Endosomes LAMP-3 (Lysosome-Associated Membrane Protein 3) Promotes the Intracellular Proliferation of Salmonella typhimurium Role for LAMP-2 in endosomal cholesterol transport.Functional analysis of lysosomes during mouse preimplantation embryo development.Visualization of cholesterol deposits in lysosomes of Niemann-Pick type C fibroblasts using recombinant perfringolysin O.Determination of protein regions responsible for interactions of amelogenin with CD63 and LAMP1.Deletion of Slc26a1 and Slc26a7 Delays Enamel Mineralization in Mice.Kinetic evidence that newly-synthesized endogenous lysosome-associated membrane protein-1 (LAMP-1) first transits early endosomes before it is delivered to lysosomes.Asparagine-linked oligosaccharides protect Lamp-1 and Lamp-2 from intracellular proteolysis.Disturbed cholesterol traffic but normal proteolytic function in LAMP-1/LAMP-2 double-deficient fibroblasts.LAMP proteins are required for fusion of lysosomes with phagosomes Regional deficiencies in chaperone-mediated autophagy underlie α-synuclein aggregation and neurodegeneration.Autophagy proteins LC3B, ATG5 and ATG12 participate in quality control after mitochondrial damage and influence lifespan.Regulation of lamp2a levels in the lysosomal membrane.

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Normal lysosomal morphology and function in LAMP-1-deficient mice

http://www.wikidata.org/entity/Q28142071

description

1999 nî lūn-bûn

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1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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1999 թվականի ապրիլին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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Normal lysosomal morphology and function in LAMP-1-deficient mice

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Normal lysosomal morphology and function in LAMP-1-deficient mice

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Normal lysosomal morphology and function in LAMP-1-deficient mice

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type

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Normal lysosomal morphology and function in LAMP-1-deficient mice

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Normal lysosomal morphology and function in LAMP-1-deficient mice

@en

Normal lysosomal morphology and function in LAMP-1-deficient mice

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prefLabel

Normal lysosomal morphology and function in LAMP-1-deficient mice

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Normal lysosomal morphology and function in LAMP-1-deficient mice

@en

Normal lysosomal morphology and function in LAMP-1-deficient mice

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Journal of Biological Chemistry

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Normal lysosomal morphology and function in LAMP-1-deficient mice

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Derived protein sequence, oligosaccharides, and membrane insertion of the 120-kDa lysosomal membrane glycoprotein (lgp120): identification of a highly conserved family of lysosomal membrane glycoproteins

The lysosomal membrane glycoproteins Lamp-1 and Lamp-2 are present in mobilizable organelles, but are absent from the azurophil granules of human neutrophils

Molecular cloning of cDNAs encoding lamp A, a human lysosomal membrane glycoprotein with apparent Mr approximately equal to 120,000

Cytotoxic T lymphocyte granules are secretory lysosomes, containing both perforin and granzymes

Purification of two glycoproteins expressing beta 1-6 branched Asn-linked oligosaccharides from metastatic tumour cells

HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system

Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells

Interrelationships of the pathways of mRNA decay and translation in eukaryotic cells

Vgr-1, a mammalian gene related to Xenopus Vg-1, is a member of the transforming growth factor beta gene superfamily

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