| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/PMIC.201000196 |
| P953 | full work available online at | https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpmic.201000196 |
| https://onlinelibrary.wiley.com/doi/full/10.1002/pmic.201000196 | ||
| P3181 | OpenCitations bibliographic resource ID | 2103445 |
| P698 | PubMed publication ID | 20957757 |
| P50 | author | Paul Saftig | Q28468939 |
| Bernd Schröder | Q89671442 | ||
| P2093 | author name string | Andrej Hasilik | |
| Christian Wrocklage | |||
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| Functional characterization of wild-type and mutant human sialin | Q37671844 | ||
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| 2-D DIGE analyses of enriched secretory lysosomes reveal heterogeneous profiles of functionally relevant proteins in leukemic and activated human NK cells | Q39957412 | ||
| Vesicular localization of the rat ATP-binding cassette half-transporter rAbcb6. | Q40030659 | ||
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| Organelle proteomics: identification of the exocytic machinery associated with the natural killer cell secretory lysosome | Q40175915 | ||
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| Proteasome inhibition by lipofuscin/ceroid during postmitotic aging of fibroblasts | Q40864003 | ||
| Mouse transporter protein, a membrane protein that regulates cellular multidrug resistance, is localized to lysosomes | Q40923295 | ||
| Lipofuscin (aging) pigment granules of the newborn human liver | Q41106603 | ||
| The discovery of lysosomes | Q41438482 | ||
| Sorting of endocytosed transferrin and asialoglycoprotein occurs immediately after internalization in HepG2 cells | Q41517247 | ||
| Two species of lysosomal organelles in cultured human fibroblasts | Q41674466 | ||
| The mannose 6-phosphate glycoprotein proteome | Q41820034 | ||
| LAMP proteins are required for fusion of lysosomes with phagosomes | Q41876261 | ||
| Cd2+, Mn2+, Ni2+ and Se2+ toxicity to Saccharomyces cerevisiae lacking YPK9p the orthologue of human ATP13A2 | Q41899742 | ||
| Lysosome-associated protein transmembrane 4 alpha (LAPTM4 alpha) requires two tandemly arranged tyrosine-based signals for sorting to lysosomes | Q42157567 | ||
| The human urine mannose 6-phosphate glycoproteome | Q42836499 | ||
| Rate of accumulation of cardiac lipofuscin in the aging canine | Q43989340 | ||
| Potential role of retinal pigment epithelial lipofuscin accumulation in age-related macular degeneration | Q44756796 | ||
| Functional characterization of novel human and mouse equilibrative nucleoside transporters (hENT3 and mENT3) located in intracellular membranes | Q45258087 | ||
| Quantitative and dynamic assessment of the contribution of the ER to phagosome formation | Q45345589 | ||
| A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases | Q22010865 | ||
| Human NRAMP2/DMT1, which mediates iron transport across endosomal membranes, is localized to late endosomes and lysosomes in HEp-2 cells | Q22253465 | ||
| Identification of HE1 as the second gene of Niemann-Pick C disease | Q24290663 | ||
| Combinatorial SNARE complexes with VAMP7 or VAMP8 define different late endocytic fusion events. | Q24292734 | ||
| Integral and associated lysosomal membrane proteins | Q24295014 | ||
| SPPL2a and SPPL2b promote intramembrane proteolysis of TNFalpha in activated dendritic cells to trigger IL-12 production | Q24296666 | ||
| Molecular and functional characterization of SLC26A11, a sodium-independent sulfate transporter from high endothelial venules | Q24297211 | ||
| Identification of a lysosomal peptide transport system induced during dendritic cell development | Q24299256 | ||
| The identification and characterization of two phosphatidylinositol-4,5-bisphosphate 4-phosphatases | Q24299329 | ||
| Zinc transporter 2 (SLC30A2) can suppress the vesicular zinc defect of adaptor protein 3-depleted fibroblasts by promoting zinc accumulation in lysosomes | Q24299648 | ||
| Identification of sites of mannose 6-phosphorylation on lysosomal proteins | Q24300525 | ||
| LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase | Q24300793 | ||
| Proteomic characterization of the human centrosome by protein correlation profiling | Q24301045 | ||
| Novel small GTPase subfamily capable of associating with tubulin is required for chromosome segregation | Q24302007 | ||
| Identification of a mammalian mitochondrial porphyrin transporter | Q24305008 | ||
| Molecular characterisation of 'transmembrane protein 192' (TMEM192), a novel protein of the lysosomal membrane | Q24305928 | ||
| Biosynthesis and Intracellular Targeting of the CLN3 Protein Defective in Batten Disease | Q24310339 | ||
| Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes | Q24311444 | ||
| Association of Mutations in a Lysosomal Protein with Classical Late-Infantile Neuronal Ceroid Lipofuscinosis | Q24311617 | ||
| Human ABC transporter isoform B6 (ABCB6) localizes primarily in the Golgi apparatus | Q24314379 | ||
| Transport of LAPTM5 to lysosomes requires association with the ubiquitin ligase Nedd4, but not LAPTM5 ubiquitination | Q24318243 | ||
| Human ABCB6 localizes to both the outer mitochondrial membrane and the plasma membrane | Q24322981 | ||
| A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis | Q24322985 | ||
| A gene network regulating lysosomal biogenesis and function | Q24339409 | ||
| The lysosomal trafficking of sphingolipid activator proteins (SAPs) is mediated by sortilin | Q24594134 | ||
| Identification and characterization of a lysosomal transporter for small neutral amino acids | Q24631129 | ||
| Identification of a vesicular aspartate transporter | Q24646582 | ||
| Natural resistance to infection with intracellular pathogens: the Nramp1 protein is recruited to the membrane of the phagosome | Q24670206 | ||
| Identification of the gene encoding the enzyme deficient in mucopolysaccharidosis IIIC (Sanfilippo disease type C) | Q24671695 | ||
| Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome) | Q24672287 | ||
| The phagosome proteome: insight into phagosome functions | Q24674883 | ||
| Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8 | Q24676012 | ||
| The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter | Q24676713 | ||
| Initial insight into the function of the lysosomal 66.3 kDa protein from mouse by means of X-ray crystallography | Q27657154 | ||
| Autophagy in the Pathogenesis of Disease | Q27860558 | ||
| Cystinosin, the protein defective in cystinosis, is a H(+)-driven lysosomal cystine transporter | Q27937730 | ||
| TMEM74, a lysosome and autophagosome protein, regulates autophagy | Q28114954 | ||
| Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase | Q28116395 | ||
| Proteomic analysis of early melanosomes: identification of novel melanosomal proteins | Q28184384 | ||
| Lysosomal membrane proteins | Q28190556 | ||
| Quantitative mass spectrometry in proteomics: a critical review | Q28238800 | ||
| Roles of LAMP-1 and LAMP-2 in lysosome biogenesis and autophagy | Q28263676 | ||
| Isolation of a novel gene underlying Batten disease, CLN3. The International Batten Disease Consortium | Q28288921 | ||
| Cloning of a lymphatic peptide/histidine transporter | Q28364223 | ||
| Isolation of the major subcellular organelles from mouse liver using Nycodenz gradients without the use of an ultracentrifuge | Q45366480 | ||
| "Subcellular proteomics" of neuromelanin granules isolated from the human brain | Q46455513 | ||
| Comparison of label-free methods for quantifying human proteins by shotgun proteomics. | Q46568113 | ||
| Isolation of Golgi membranes from tissues and cells by differential and density gradient centrifugation | Q46785503 | ||
| Isolation of lysosomes from tissues and cells by differential and density gradient centrifugation | Q46785510 | ||
| A method to assess the lysosomal residence of proteins in cultured cells | Q46848913 | ||
| Characterisation of lipofuscin-like lysosomal inclusion bodies from human placenta | Q52575698 | ||
| Processing of human cathepsin D in lysosomes in vitro. | Q54453142 | ||
| Neuronal ceroid lipofuscinoses | Q56566989 | ||
| Isolation of a novel gene underlying batten disease, CLN3 | Q56804260 | ||
| A Proteomic Analysis of Lysosomal Integral Membrane Proteins Reveals the Diverse Composition of the Organelle | Q57372787 | ||
| Chaperone-Mediated Autophagy | Q57376122 | ||
| Two-dimensional mapping and microsequencing of lysosomal proteins from human placenta | Q58039502 | ||
| Proteomic Analysis of Membrane-Associated Proteins from Rat Liver Autophagosomes | Q63313636 | ||
| Stimulation of the biosynthesis of lactosamine repeats in glycoproteins in differentiating U937 cells and its suppression in the presence of NH4Cl | Q67901622 | ||
| Rupture of rat liver lysosomes mediated by L-amino acid esters | Q69595430 | ||
| Isolation of highly purified rat liver lysosomal membranes using two Percoll gradients | Q69810866 | ||
| Method for the isolation of iron-loaded lysosomes from rat liver | Q70037544 | ||
| Purification of lysosomal membrane proteins from human placenta | Q71757470 | ||
| The preparation of subcellular organelles from mouse liver in self-generated gradients of iodixanol | Q72851806 | ||
| Lysosomal proteolysis of prosaposin, the precursor of saposins (sphingolipid activator proteins): its mechanism and inhibition by ganglioside | Q73323611 | ||
| Lysosomal membranes from beige mice contain higher than normal levels of endoplasmic reticulum proteins | Q79491764 | ||
| The lysosomal trafficking of acid sphingomyelinase is mediated by sortilin and mannose 6-phosphate receptor | Q79759115 | ||
| A protocol for combined delipidation and subfractionation of membrane proteins using organic solvents | Q80139032 | ||
| Proteomics analysis of serum from mutant mice reveals lysosomal proteins selectively transported by each of the two mannose 6-phosphate receptors | Q81234547 | ||
| Identification and validation of mannose 6-phosphate glycoproteins in human plasma reveal a wide range of lysosomal and non-lysosomal proteins | Q83367020 | ||
| An ascorbate-reducible cytochrome b561 is localized in macrophage lysosomes | Q28505660 | ||
| Intracellular localization of p40, a protein identified in a preparation of lysosomal membranes | Q28507805 | ||
| Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution | Q28508163 | ||
| NCU-G1 is a highly glycosylated integral membrane protein of the lysosome | Q28509778 | ||
| ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function | Q28512374 | ||
| Presenilin-1, Nicastrin, Amyloid Precursor Protein, and γ-Secretase Activity Are Co-localized in the Lysosomal Membrane | Q28568133 | ||
| Rat brain contains high levels of mannose-6-phosphorylated glycoproteins including lysosomal enzymes and palmitoyl-protein thioesterase, an enzyme implicated in infantile neuronal lipofuscinosis | Q28570730 | ||
| Biochemical characterization and lysosomal localization of the mannose-6-phosphate protein p76 (hypothetical protein LOC196463) | Q28588547 | ||
| A model for random sampling and estimation of relative protein abundance in shotgun proteomics | Q29547316 | ||
| Signals for sorting of transmembrane proteins to endosomes and lysosomes | Q29547469 | ||
| Comparative Bioinformatics Analyses and Profiling of Lysosome-Related Organelle Proteomes | Q30445187 | ||
| Towards a human repertoire of monocytic lysosomal proteins | Q30962551 | ||
| High throughput two-dimensional blue-native electrophoresis: a tool for functional proteomics of mitochondria and signaling complexes | Q31106305 | ||
| The human brain mannose 6-phosphate glycoproteome: a complex mixture composed of multiple isoforms of many soluble lysosomal proteins | Q31155960 | ||
| Proteome analysis of lipofuscin in human retinal pigment epithelial cells | Q33184588 | ||
| Identification of novel lysosomal matrix proteins by proteome analysis | Q33222882 | ||
| Proteomic analysis of lysosomal acid hydrolases secreted by osteoclasts: implications for lytic enzyme transport and bone metabolism | Q33224913 | ||
| Examining the proteins of functional retinal lipofuscin using proteomic analysis as a guide for understanding its origin | Q33230359 | ||
| High-throughput functional screening for autophagy-related genes and identification of TM9SF1 as an autophagosome-inducing gene | Q33386723 | ||
| Mucolipins: Intracellular TRPML1-3 channels | Q33838349 | ||
| Lysosomal transport disorders | Q33948573 | ||
| A mammalian organelle map by protein correlation profiling | Q33995084 | ||
| The structure and function of the Niemann-Pick C1 protein | Q34043087 | ||
| The large-scale separation of peroxisomes, mitochondria, and lysosomes from the livers of rats injected with triton WR-1339. Improved isolation procedures, automated analysis, biochemical and morphological properties of fractions | Q34205999 | ||
| ??? | Q22254154 | ||
| GEE MV: Rate and magnitude of age pigment accumulation in the human myocardium | Q34250756 | ||
| Lipofuscin | Q34321294 | ||
| An N-terminally acetylated Arf-like GTPase is localised to lysosomes and affects their motility | Q34502171 | ||
| The Arf-family protein, Arl8b, is involved in the spatial distribution of lysosomes | Q34519744 | ||
| TMEM166, a novel transmembrane protein, regulates cell autophagy and apoptosis | Q34626965 | ||
| Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism | Q34919649 | ||
| Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function | Q34996827 | ||
| ER-mediated phagocytosis: a new membrane for new functions | Q35096184 | ||
| Lysosomal storage disorders | Q36027312 | ||
| Isolation and preliminary characterization of the major membrane boundaries of the endocytic pathway in lymphocytes. | Q36223921 | ||
| The dynamic phagosomal proteome and the contribution of the endoplasmic reticulum | Q36276856 | ||
| You say lipofuscin, we say ceroid: defining autofluorescent storage material | Q36385244 | ||
| The lysosomal-mitochondrial axis theory of postmitotic aging and cell death | Q36493763 | ||
| TRPML and lysosomal function | Q36738367 | ||
| Lysosome-related organelles: driving post-Golgi compartments into specialisation | Q36880252 | ||
| Lysosomes: fusion and function | Q36885390 | ||
| Membrane proteomics of phagosomes suggests a connection to autophagy | Q36964264 | ||
| V-ATPase functions in normal and disease processes | Q37008545 | ||
| Autophagy, amyloidogenesis and Alzheimer disease | Q37011121 | ||
| The role of autophagy-lysosome pathway in neurodegeneration associated with Parkinson's disease | Q37054679 | ||
| Proteomic and phototoxic characterization of melanolipofuscin: correlation to disease and model for its origin | Q37097697 | ||
| Deficiency of the tetraspanin CD63 associated with kidney pathology but normal lysosomal function | Q37099908 | ||
| Molecular physiology and pathophysiology of lysosomal membrane transporters | Q37143215 | ||
| Autophagy in atherosclerosis. | Q37167775 | ||
| Proteomics of the lysosome | Q37196950 | ||
| P433 | issue | 22 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Solute carrier family 35 member F6 | Q21104967 |
| Transmembrane protein 63A | Q21112036 | ||
| Solute carrier family 26 member 11 | Q21121330 | ||
| P304 | page(s) | 4053-76 | |
| P577 | publication date | 2010-10-19 | |
| 2010-11-01 | |||
| P1433 | published in | Proteomics | Q15614164 |
| P1476 | title | The proteome of lysosomes | |
| P478 | volume | 10 |
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| Q39125906 | Accounting for Protein Subcellular Localization: A Compartmental Map of the Rat Liver Proteome. |
| Q36910788 | An Extended Proteome Map of the Lysosomal Membrane Reveals Novel Potential Transporters |
| Q46020421 | Analysis of N- and O-Glycosylation of Lysosomal Glycoproteins. |
| Q28551083 | Analysis of the Proteolytic Processing of ABCA3: Identification of Cleavage Site and Involved Proteases |
| Q50503440 | Analyzing Lysosomes in Live Cells |
| Q26774998 | Antimicrobial Mechanisms of Macrophages and the Immune Evasion Strategies of Staphylococcus aureus |
| Q36506704 | Atg9 is required for intraluminal vesicles in amphisomes and autolysosomes |
| Q37659097 | Autophagy and Schizophrenia: A Closer Look at How Dysregulation of Neuronal Cell Homeostasis Influences the Pathogenesis of Schizophrenia |
| Q28659840 | Boning up on autophagy: the role of autophagy in skeletal biology |
| Q39237735 | Cathepsins in digestive cancers |
| Q38080980 | Cell biology and function of neuronal ceroid lipofuscinosis-related proteins |
| Q36847458 | Cell healing: Calcium, repair and regeneration |
| Q51547401 | Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways |
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| Q49914916 | Co-deficiency of Lysosomal Mucolipins 3 and 1 in Cochlear Hair Cells Diminishes Outer Hair Cell Longevity and Accelerates Age-Related Hearing Loss. |
| Q37121962 | Complementation of Arginine Auxotrophy for Genetic Transformation of Coxiella burnetii by Use of a Defined Axenic Medium |
| Q37702538 | Comprehensive proteome analysis of lysosomes reveals the diverse function of macrophages in immune responses |
| Q44612676 | Control of Phagocytosis by Microbial Pathogens. |
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| Q38974926 | Emerging connections between RNA and autophagy. |
| Q39524168 | ErbB2-associated changes in the lysosomal proteome. |
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