| scholarly article | Q13442814 |
| P2093 | author name string | Daniel N Hebert | |
| James H Cormier | |||
| Taku Tamura | |||
| P2860 | cites work | Role of EDEM in the release of misfolded glycoproteins from the calnexin cycle | Q24296412 |
| Derlin-2 and Derlin-3 are regulated by the mammalian unfolded protein response and are required for ER-associated degradation | Q24302539 | ||
| Human EDEM2, a novel homolog of family 47 glycosidases, is involved in ER-associated degradation of glycoproteins | Q24313639 | ||
| Human XTP3-B forms an endoplasmic reticulum quality control scaffold with the HRD1-SEL1L ubiquitin ligase complex and BiP | Q24316328 | ||
| A dual role for EDEM1 in the processing of rod opsin | Q24320047 | ||
| Cotranslational and posttranslational N-glycosylation of polypeptides by distinct mammalian OST isoforms | Q24321464 | ||
| EDEM1 recognition and delivery of misfolded proteins to the SEL1L-containing ERAD complex | Q24338144 | ||
| A novel ER alpha-mannosidase-like protein accelerates ER-associated degradation | Q24522524 | ||
| The concept of translocational regulation | Q24654677 | ||
| One step at a time: endoplasmic reticulum-associated degradation | Q24658302 | ||
| EDEM1 reveals a quality control vesicular transport pathway out of the endoplasmic reticulum not involving the COPII exit sites | Q24683239 | ||
| N-linked glycans direct the cotranslational folding pathway of influenza hemagglutinin. | Q27863759 | ||
| Defining the glycan destruction signal for endoplasmic reticulum-associated degradation | Q27932810 | ||
| Roles of protein-disulfide isomerase-mediated disulfide bond formation of yeast Mnl1p in endoplasmic reticulum-associated degradation | Q27934273 | ||
| Htm1 protein generates the N-glycan signal for glycoprotein degradation in the endoplasmic reticulum | Q27939524 | ||
| Distinct retrieval and retention mechanisms are required for the quality control of endoplasmic reticulum protein folding | Q27939944 | ||
| In and Out of the ER: Protein Folding, Quality Control, Degradation, and Related Human Diseases | Q28109625 | ||
| EDEM as an acceptor of terminally misfolded glycoproteins released from calnexin | Q28212764 | ||
| Determination of the distance between the oligosaccharyltransferase active site and the endoplasmic reticulum membrane | Q28267028 | ||
| A novel stress-induced EDEM variant regulating endoplasmic reticulum-associated glycoprotein degradation | Q28296585 | ||
| EDEM1 accelerates the trimming of alpha1,2-linked mannose on the C branch of N-glycans | Q28510507 | ||
| ERdj5 is required as a disulfide reductase for degradation of misfolded proteins in the ER | Q28512215 | ||
| EDEM3, a soluble EDEM homolog, enhances glycoprotein endoplasmic reticulum-associated degradation and mannose trimming | Q28593084 | ||
| Locating proteins in the cell using TargetP, SignalP and related tools | Q29547300 | ||
| Roles of N-linked glycans in the endoplasmic reticulum | Q29616458 | ||
| Stringent requirement for HRD1, SEL1L, and OS-9/XTP3-B for disposal of ERAD-LS substrates | Q33615098 | ||
| Signal sequence insufficiency contributes to neurodegeneration caused by transmembrane prion protein | Q33689595 | ||
| Oligosaccharide modification in the early secretory pathway directs the selection of a misfolded glycoprotein for degradation by the proteasome | Q33852597 | ||
| Quality and quantity control at the endoplasmic reticulum | Q34090425 | ||
| The organizing principle in the formation of the T cell receptor-CD3 complex. | Q34167740 | ||
| Transient, lectin-like association of calreticulin with folding intermediates of cellular and viral glycoproteins | Q34451461 | ||
| The molecular chaperone calnexin facilitates folding and assembly of class I histocompatibility molecules | Q35846706 | ||
| Posttranscriptional regulation of hepatitis B virus replication by the precore protein | Q35874866 | ||
| The glycan code of the endoplasmic reticulum: asparagine-linked carbohydrates as protein maturation and quality-control tags | Q36153965 | ||
| Stage- and ribosome-specific alterations in nascent chain-Sec61p interactions accompany translocation across the ER membrane | Q36235677 | ||
| The number and location of glycans on influenza hemagglutinin determine folding and association with calnexin and calreticulin | Q36276590 | ||
| Intracellular protein topogenesis | Q36360251 | ||
| In vitro translation and assembly of a complete T cell receptor-CD3 complex | Q36380431 | ||
| The surprising complexity of signal sequences | Q36571413 | ||
| SEL1L nucleates a protein complex required for dislocation of misfolded glycoproteins | Q36858538 | ||
| Protein-protein interactions in the membrane: sequence, structural, and biological motifs | Q37210616 | ||
| The mammalian UPR boosts glycoprotein ERAD by suppressing the proteolytic downregulation of ER mannosidase I. | Q37289488 | ||
| Glycoprotein folding, quality control and ER-associated degradation | Q37555655 | ||
| ERAD substrates: which way out? | Q37660718 | ||
| Chaperone function of calreticulin when expressed in the endoplasmic reticulum as the membrane-anchored and soluble forms. | Q38292055 | ||
| Basal autophagy is involved in the degradation of the ERAD component EDEM1. | Q39876239 | ||
| Segregation and rapid turnover of EDEM1 by an autophagy-like mechanism modulates standard ERAD and folding activities | Q39985945 | ||
| EDEM1 regulates ER-associated degradation by accelerating de-mannosylation of folding-defective polypeptides and by inhibiting their covalent aggregation. | Q40229528 | ||
| Regulation of protein compartmentalization expands the diversity of protein function | Q40366867 | ||
| The cotranslational maturation of the type I membrane glycoprotein tyrosinase: the heat shock protein 70 system hands off to the lectin-based chaperone system | Q40409191 | ||
| Degradation of trafficking-defective long QT syndrome type II mutant channels by the ubiquitin-proteasome pathway. | Q40448063 | ||
| Calnexin and calreticulin promote folding, delay oligomerization and suppress degradation of influenza hemagglutinin in microsomes. | Q41065377 | ||
| Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies | Q41854466 | ||
| Translation rate of human tyrosinase determines its N-linked glycosylation level | Q43509483 | ||
| Carbohydrates act as sorting determinants in ER-associated degradation of tyrosinase | Q44909736 | ||
| Coronaviruses Hijack the LC3-I-positive EDEMosomes, ER-derived vesicles exporting short-lived ERAD regulators, for replication | Q44986570 | ||
| Signal sequences initiate the pathway of maturation in the endoplasmic reticulum lumen. | Q46274296 | ||
| A frameshift mutation results in a truncated alpha 1-antitrypsin that is retained within the rough endoplasmic reticulum | Q68093404 | ||
| The alpha chain of the T cell antigen receptor is degraded in the cytosol | Q73574925 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 28 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 24906-24915 | |
| P577 | publication date | 2011-06-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Characterization of early EDEM1 protein maturation events and their functional implications | |
| P478 | volume | 286 |
| Q30360183 | A Golgi-localized mannosidase (MAN1B1) plays a non-enzymatic gatekeeper role in protein biosynthetic quality control. |
| Q42827982 | A shared endoplasmic reticulum-associated degradation pathway involving the EDEM1 protein for glycosylated and nonglycosylated proteins |
| Q48316566 | Arabidopsis Class I α-Mannosidases MNS4 and MNS5 Are Involved in Endoplasmic Reticulum-Associated Degradation of Misfolded Glycoproteins |
| Q28078319 | Arms Race between Enveloped Viruses and the Host ERAD Machinery |
| Q28078736 | Co- and Post-Translational Protein Folding in the ER |
| Q41720457 | Dual control of pcdh8l/PCNS expression and function in Xenopus laevis neural crest cells by adam13/33 via the transcription factors tfap2α and arid3a |
| Q57705922 | EDEM1's mannosidase-like domain binds ERAD client proteins in a redox-sensitive manner and possesses catalytic activity |
| Q39012161 | ERADication of EDEM1 occurs by selective autophagy and requires deglycosylation by cytoplasmic peptide N-glycanase. |
| Q36732745 | Extreme C-terminal sites are posttranslocationally glycosylated by the STT3B isoform of the OST. |
| Q36282189 | Flagging and docking: dual roles for N-glycans in protein quality control and cellular proteostasis |
| Q38606832 | Glycosylation-directed quality control of protein folding |
| Q37583253 | Lipid disequilibrium disrupts ER proteostasis by impairing ERAD substrate glycan trimming and dislocation |
| Q92192855 | Profiling Optimal Conditions for Capturing EDEM Proteins Complexes in Melanoma Using Mass Spectrometry |
| Q38103530 | Protein folding in the endoplasmic reticulum |
| Q24295118 | TMTC1 and TMTC2 are novel endoplasmic reticulum tetratricopeptide repeat-containing adapter proteins involved in calcium homeostasis |
| Q38507330 | The Role of Lectin-Carbohydrate Interactions in the Regulation of ER-Associated Protein Degradation. |
| Q24339440 | The role of EDEM2 compared with EDEM1 in ricin transport from the endoplasmic reticulum to the cytosol |
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