Pages that link to "Q33222882"

The following pages link to Identification of novel lysosomal matrix proteins by proteome analysis (Q33222882):

Displaying 49 items.

• The neuronal ceroid lipofuscinosis protein CLN5: new insights into cellular maturation, transport, and consequences of mutations (Q24294224) (← links)
• Identification of sites of mannose 6-phosphorylation on lysosomal proteins (Q24300525) (← links)
• The proteome of lysosomes (Q24303943) (← links)
• Arylsulfatase G, a novel lysosomal sulfatase (Q24315039) (← links)
• Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1 (Q27316913) (← links)
• Initial insight into the function of the lysosomal 66.3 kDa protein from mouse by means of X-ray crystallography (Q27657154) (← links)
• Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins (Q28115540) (← links)
• Intracellular localization of p40, a protein identified in a preparation of lysosomal membranes (Q28507805) (← links)
• Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution (Q28508163) (← links)
• NCU-G1 is a highly glycosylated integral membrane protein of the lysosome (Q28509778) (← links)
• Biochemical characterization and lysosomal localization of the mannose-6-phosphate protein p76 (hypothetical protein LOC196463) (Q28588547) (← links)
• Demonstration of lysosomal localization for the mammalian ependymin-related protein using classical approaches combined with a novel density shift method (Q28589614) (← links)
• hLGDB: a database of human lysosomal genes and their regulation. (Q30486090) (← links)
• Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis (Q33558217) (← links)
• The Mycobacterium bovis bacille Calmette-Guerin phagosome proteome (Q33598006) (← links)
• The role of N-glycosylation in folding, trafficking, and functionality of lysosomal protein CLN5. (Q34994610) (← links)
• Potential pitfalls and solutions for use of fluorescent fusion proteins to study the lysosome (Q35106403) (← links)
• The Niemann-Pick type C2 protein loads isoglobotrihexosylceramide onto CD1d molecules and contributes to the thymic selection of NKT cells (Q36229257) (← links)
• TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways (Q36247028) (← links)
• Microtargeting cancer metabolism: opening new therapeutic windows based on lipid metabolism (Q36503853) (← links)
• An extended proteome map of the lysosomal membrane reveals novel potential transporters (Q36910788) (← links)
• Evolution of organelle-associated protein profiling (Q37188390) (← links)
• Proteomics of the lysosome (Q37196950) (← links)
• Hyaluronan, a crucial regulator of inflammation (Q37629440) (← links)
• The yeast protein sorting pathway as an experimental model for lysosomal trafficking (Q37754779) (← links)
• Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses (Q37944570) (← links)
• Transcriptional gene network inference from a massive dataset elucidates transcriptome organization and gene function. (Q38855841) (← links)
• Topology and membrane anchoring of the lysosomal storage disease-related protein CLN5. (Q39095656) (← links)
• Exacerbating and reversing lysosomal storage diseases: from yeast to humans (Q40038745) (← links)
• Intracellular Proteolysis of Progranulin Generates Stable, Lysosomal Granulins that Are Haploinsufficient in Patients with Frontotemporal Dementia Caused by GRN Mutations (Q41455989) (← links)
• The mannose 6-phosphate glycoprotein proteome (Q41820034) (← links)
• Proteomics Insights into Autophagy. (Q42514979) (← links)
• Arylsulfatase K, a novel lysosomal sulfatase (Q42771926) (← links)
• The human urine mannose 6-phosphate glycoproteome (Q42836499) (← links)
• Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. (Q46136561) (← links)
• Cellular repressor of E1A-stimulated genes is a bona fide lysosomal protein which undergoes proteolytic maturation during its biosynthesis. (Q46487767) (← links)
• Organellar Omics-A Reviving Strategy to Untangle the Biomolecular Complexity of the Cell (Q47975495) (← links)
• Stat3 mediated alterations in lysosomal membrane protein composition (Q48533476) (← links)
• Tissue expression of the novel serine carboxypeptidase Scpep1. (Q48660692) (← links)
• Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways (Q51547401) (← links)
• Molecular and cellular characterization of novel α-mannosidosis mutations (Q51768426) (← links)
• The transport of soluble lysosomal hydrolases from the Golgi complex to lysosomes (Q57201215) (← links)
• The Structure and Biological Function of CREG (Q58707931) (← links)
• Crystal structures of human lysosomal EPDR1 reveal homology with the superfamily of bacterial lipoprotein transporters (Q61799229) (← links)
• Identification and validation of mannose 6-phosphate glycoproteins in human plasma reveal a wide range of lysosomal and non-lysosomal proteins (Q83367020) (← links)
• Induction of endosomal/lysosomal pathways in differentiating osteoblasts as revealed by combined proteomic and transcriptomic analyses (Q84649365) (← links)
• Comprehensive draft of the mouse embryonic fibroblast lysosomal proteome by mass spectrometry based proteomics (Q89900259) (← links)
• Structures of three ependymin-related proteins suggest their function as a hydrophobic molecule binder (Q91974208) (← links)
• p67: A Cryptic Lysosomal Hydrolase in Trypanosoma brucei? (Q100724547) (← links)