| P50 | author | Pirjo M Apaja | Q57051463 |
| | Gergely L Lukacs | Q38322272 |
| P2093 | author name string | Haijin Xu | |
| P2860 | cites work | The co-chaperone CHIP regulates protein triage decisions mediated by heat-shock proteins | Q24290709 |
| | c-Cbl mediates ubiquitination, degradation, and down-regulation of human protease-activated receptor 2 | Q24294848 |
| | Folding efficiency is rate-limiting in dopamine D4 receptor biogenesis | Q24297696 |
| | VHS domains of ESCRT-0 cooperate in high-avidity binding to polyubiquitinated cargo | Q24299091 |
| | The E3 ubiquitin ligase AIP4 mediates ubiquitination and sorting of the G protein-coupled receptor CXCR4 | Q24299260 |
| | CHIP is associated with Parkin, a gene responsible for familial Parkinson's disease, and enhances its ubiquitin ligase activity | Q24302505 |
| | Itch/AIP4 mediates Deltex degradation through the formation of K29-linked polyubiquitin chains | Q24306305 |
| | Protein quality control: U-box-containing E3 ubiquitin ligases join the fold | Q44061660 |
| | Demonstration of two distinct high molecular weight proteases in rabbit reticulocytes, one of which degrades ubiquitin conjugates | Q47198618 |
| | Dual degradation mechanisms ensure disposal of NHE6 mutant protein associated with neurological disease. | Q50335672 |
| | Structure and interactions of the helical and U-box domains of CHIP, the C terminus of HSP70 interacting protein. | Q51586726 |
| | Vasopressin V2 receptor mutants that cause X-linked nephrogenic diabetes insipidus: analysis of expression, processing, and function. | Q54580161 |
| | Oxytocin and Vasopressin V1a and V2 Receptors Form Constitutive Homo- and Heterodimers during Biosynthesis | Q56648628 |
| | Endocytosis | Q57374715 |
| | Quality control of a mutant plasma membrane ATPase: ubiquitylation prevents cell-surface stability | Q57375268 |
| | The structural stability of a protein is an important determinant of its proteolytic susceptibility in Escherichia coli | Q69496214 |
| | The stabilization mechanism of mutant-type p53 by impaired ubiquitination: the loss of wild-type p53 function and the hsp90 association | Q73171130 |
| | The ubiquitin-protein ligases Nedd4 and Nedd4-2 show similar ubiquitin-conjugating enzyme specificities | Q81594841 |
| | Nedd4 mediates agonist-dependent ubiquitination, lysosomal targeting, and degradation of the beta2-adrenergic receptor | Q24320318 |
| | Molecular pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts: mutations in MLC1 cause folding defects | Q24642920 |
| | Quantitative proteomics reveals the function of unconventional ubiquitin chains in proteasomal degradation | Q24643067 |
| | Misfolding diverts CFTR from recycling to degradation: quality control at early endosomes | Q24676764 |
| | Ubiquitin chain editing revealed by polyubiquitin linkage-specific antibodies | Q27651780 |
| | Mechanisms underlying ubiquitination | Q27860656 |
| | A transmembrane ubiquitin ligase required to sort membrane proteins into multivesicular bodies | Q27931399 |
| | ESCRT ubiquitin-binding domains function cooperatively during MVB cargo sorting | Q27931999 |
| | Cytoplasmic protein quality control degradation mediated by parallel actions of the E3 ubiquitin ligases Ubr1 and San1 | Q27932129 |
| | Ubiquitin-dependent sorting into the multivesicular body pathway requires the function of a conserved endosomal protein sorting complex, ESCRT-I. | Q27939053 |
| | Arrestin-related ubiquitin-ligase adaptors regulate endocytosis and protein turnover at the cell surface. | Q27939550 |
| | Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants | Q28115855 |
| | ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration | Q28117494 |
| | Sensitivity of mature Erbb2 to geldanamycin is conferred by its kinase domain and is mediated by the chaperone protein Hsp90 | Q28143497 |
| | Identification of the ubiquitin carrier proteins, E2s, involved in signal-induced conjugation and subsequent degradation of IkappaBalpha | Q28144122 |
| | Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus | Q28183211 |
| | Regulation of receptor fate by ubiquitination of activated beta 2-adrenergic receptor and beta-arrestin | Q28190513 |
| | ErbB2 degradation mediated by the co-chaperone protein CHIP | Q28208008 |
| | Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus | Q28208115 |
| | Luteinizing hormone receptor ectodomain splice variant misroutes the full-length receptor into a subcompartment of the endoplasmic reticulum. | Q28573360 |
| | Derlin-dependent accumulation of integral membrane proteins at cell surfaces | Q28588156 |
| | Ubiquitin-binding domains - from structures to functions | Q29614829 |
| | The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation | Q29616141 |
| | Biological and chemical approaches to diseases of proteostasis deficiency | Q29616633 |
| | The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins | Q29617399 |
| | Pathways of chaperone-mediated protein folding in the cytosol | Q29618887 |
| | Quality control in the endoplasmic reticulum | Q29619929 |
| | Chaperone functions of the E3 ubiquitin ligase CHIP. | Q30362083 |
| | Clathrin-independent endocytosis of ErbB2 in geldanamycin-treated human breast cancer cells | Q30439237 |
| | Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartments. | Q31742906 |
| | Inefficient quality control of thermosensitive proteins on the plasma membrane | Q33425200 |
| | Ubiquitin-mediated targeting of a mutant plasma membrane ATPase, Pma1-7, to the endosomal/vacuolar system in yeast | Q33693280 |
| | Evasion of endoplasmic reticulum surveillance makes Wsc1p an obligate substrate of Golgi quality control | Q33761462 |
| | ER protein quality control and proteasome-mediated protein degradation | Q33794243 |
| | Down-regulation of cell surface receptors is modulated by polar residues within the transmembrane domain | Q33912615 |
| | A mutant plasma membrane ATPase, Pma1-10, is defective in stability at the yeast cell surface | Q33929848 |
| | Yeast mutants affecting possible quality control of plasma membrane proteins | Q33957947 |
| | Identification of residues on Hsp70 and Hsp90 ubiquitinated by the cochaperone CHIP | Q34048681 |
| | Cellular defenses against unfolded proteins: a cell biologist thinks about neurodegenerative diseases | Q34142252 |
| | Chaperone-dependent E3 ubiquitin ligase CHIP mediates a degradative pathway for c-ErbB2/Neu | Q34190181 |
| | ER quality control: towards an understanding at the molecular level | Q34309048 |
| | A new ticket for entry into budding vesicles-ubiquitin | Q34365247 |
| | Constitutive arrestin-mediated desensitization of a human vasopressin receptor mutant associated with nephrogenic diabetes insipidus | Q34584278 |
| | Certain pairs of ubiquitin-conjugating enzymes (E2s) and ubiquitin-protein ligases (E3s) synthesize nondegradable forked ubiquitin chains containing all possible isopeptide linkages. | Q34617875 |
| | Detecting cAMP-induced Epac activation by fluorescence resonance energy transfer: Epac as a novel cAMP indicator | Q34650064 |
| | Recognition of a single transmembrane degron by sequential quality control checkpoints | Q34814483 |
| | Secretory pathway quality control operating in Golgi, plasmalemmal, and endosomal systems | Q34970141 |
| | ER-associated degradation in protein quality control and cellular regulation | Q34970862 |
| | Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention | Q35693428 |
| | CHIP: a link between the chaperone and proteasome systems | Q35759085 |
| | High-resolution mapping of the protein interaction network for the human transcription machinery and affinity purification of RNA polymerase II-associated complexes | Q35822226 |
| | Evidence for coupled biogenesis of yeast Gap1 permease and sphingolipids: essential role in transport activity and normal control by ubiquitination | Q35942358 |
| | Plasticity of polyubiquitin recognition as lysosomal targeting signals by the endosomal sorting machinery | Q36017039 |
| | Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease | Q36119653 |
| | Site-specific ubiquitination exposes a linear motif to promote interferon-alpha receptor endocytosis | Q36176561 |
| | Retrograde transport of Golgi-localized proteins to the ER. | Q36254921 |
| | Aggregation as a determinant of protein fate in post-Golgi compartments: role of the luminal domain of furin in lysosomal targeting | Q36255053 |
| | COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments | Q36326371 |
| | Subcellular imaging of dynamic protein interactions by bioluminescence resonance energy transfer | Q36345018 |
| | ATP-dependent conjugation of reticulocyte proteins with the polypeptide required for protein degradation | Q36359536 |
| | Polyubiquitination of prolactin receptor stimulates its internalization, postinternalization sorting, and degradation via the lysosomal pathway | Q36846031 |
| | Ubiquitin-dependent sorting of integral membrane proteins for degradation in lysosomes | Q36906047 |
| | N-glycans are direct determinants of CFTR folding and stability in secretory and endocytic membrane traffic | Q37234365 |
| | Arrestins as adaptors for ubiquitination in endocytosis and sorting | Q37341630 |
| | The ubiquitylation machinery of the endoplasmic reticulum | Q37424805 |
| | Regulation of Hsp90 client proteins by a Cullin5-RING E3 ubiquitin ligase | Q37453413 |
| | Short-chain ubiquitination is associated with the degradation rate of a cell-surface-resident bile salt export pump (BSEP/ABCB11). | Q39933453 |
| | Analysis of endocytic trafficking by single-cell fluorescence ratio imaging | Q39935449 |
| | Demonstration of improvements to the bioluminescence resonance energy transfer (BRET) technology for the monitoring of G protein-coupled receptors in live cells | Q39936620 |
| | Levels of plasma membrane expression in progressive and benign mutations of the bile salt export pump (Bsep/Abcb11) correlate with severity of cholestatic diseases | Q40080714 |
| | Curcumin-induced degradation of ErbB2: A role for the E3 ubiquitin ligase CHIP and the Michael reaction acceptor activity of curcumin | Q40180822 |
| | Molecular basis of oligoubiquitin-dependent internalization of membrane proteins in Mammalian cells | Q40312393 |
| | Epsin 1 is a polyubiquitin-selective clathrin-associated sorting protein. | Q40312400 |
| | Geldanamycin stimulates internalization of ErbB2 in a proteasome-dependent way. | Q40340333 |
| | Characterization of vasopressin V2 receptor mutants in nephrogenic diabetes insipidus in a polarized cell model | Q40399721 |
| | Real-time monitoring of ubiquitination in living cells by BRET. | Q40443828 |
| | Identification of molecular determinants that modulate trafficking of DeltaF508 CFTR, the mutant ABC transporter associated with cystic fibrosis. | Q40464949 |
| | A progressive familial intrahepatic cholestasis type 2 mutation causes an unstable, temperature-sensitive bile salt export pump. | Q40607981 |
| | Regulation of V2 vasopressin receptor degradation by agonist-promoted ubiquitination | Q40636866 |
| | The role of a conserved inter-transmembrane domain interface in regulating alpha(2a)-adrenergic receptor conformational stability and cell-surface turnover | Q40819594 |
| | Peripheral protein quality control removes unfolded CFTR from the plasma membrane | Q41111670 |
| | The ubiquitin-activating enzyme is required for lysosomal degradation of cellular proteins under stress | Q41705356 |
| | Empty MHC class I molecules come out in the cold | Q41725383 |
| | CHIP is a chaperone-dependent E3 ligase that ubiquitylates unfolded protein | Q41776375 |
| | Efficient internalization of MHC I requires lysine-11 and lysine-63 mixed linkage polyubiquitin chains. | Q41825273 |
| | Arrestin-mediated endocytosis of yeast plasma membrane transporters | Q42931930 |
| | Lysine-63-linked ubiquitination is required for endolysosomal degradation of class I molecules | Q43077741 |
| | Arrestin-like proteins mediate ubiquitination and endocytosis of the yeast metal transporter Smf1. | Q43240938 |
| | Multiple roles for Rsp5p-dependent ubiquitination at the internalization step of endocytosis | Q43610822 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | quality control | Q827792 |
| P1104 | number of pages | 18 | |
| P304 | page(s) | 553-570 | |
| P577 | publication date | 2010-10-25 | |
| P1433 | published in | Journal of Cell Biology | Q1524550 |
| P1476 | title | Quality control for unfolded proteins at the plasma membrane | |
| P478 | volume | 191 | |