scholarly article | Q13442814 |
P50 | author | Maurizio Molinari | Q37379667 |
P2093 | author name string | Carmela Galli | |
Silvia Olivari | |||
Heli Alanen | |||
Lloyd Ruddock | |||
P2860 | cites work | Cloning and expression of a specific human alpha 1,2-mannosidase that trims Man9GlcNAc2 to Man8GlcNAc2 isomer B during N-glycan biosynthesis | Q22010659 |
Plasma cell differentiation requires the transcription factor XBP-1 | Q24291453 | ||
Role of EDEM in the release of misfolded glycoproteins from the calnexin cycle | Q24296412 | ||
A novel ER alpha-mannosidase-like protein accelerates ER-associated degradation | Q24522524 | ||
Structural basis for catalysis and inhibition of N-glycan processing class I alpha 1,2-mannosidases | Q27627138 | ||
Improved prediction of signal peptides: SignalP 3.0 | Q27860548 | ||
Mnl1p, an alpha -mannosidase-like protein in yeast Saccharomyces cerevisiae, is required for endoplasmic reticulum-associated degradation of glycoproteins | Q27937049 | ||
Htm1p, a mannosidase-like protein, is involved in glycoprotein degradation in yeast | Q27939809 | ||
Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradation | Q28131669 | ||
EDEM as an acceptor of terminally misfolded glycoproteins released from calnexin | Q28212764 | ||
Plasma cell differentiation and the unfolded protein response intersect at the transcription factor XBP-1 | Q28507338 | ||
Lectin control of protein folding and sorting in the secretory pathway | Q28576042 | ||
XBP-1 Regulates a Subset of Endoplasmic Reticulum Resident Chaperone Genes in the Unfolded Protein Response | Q28585314 | ||
Impairment of the ubiquitin-proteasome system by protein aggregation | Q29614556 | ||
Roles of N-linked glycans in the endoplasmic reticulum | Q29616458 | ||
Database resources of the National Center for Biotechnology | Q29618892 | ||
Setting the standards: quality control in the secretory pathway | Q29620321 | ||
Elucidation of the molecular logic by which misfolded alpha 1-antitrypsin is preferentially selected for degradation. | Q30332997 | ||
Oligosaccharide modification in the early secretory pathway directs the selection of a misfolded glycoprotein for degradation by the proteasome | Q33852597 | ||
Role of N-oligosaccharide endoplasmic reticulum processing reactions in glycoprotein folding and degradation | Q33905603 | ||
A novel lectin in the secretory pathway. An elegant mechanism for glycoprotein elimination. | Q34330208 | ||
XBP1, downstream of Blimp-1, expands the secretory apparatus and other organelles, and increases protein synthesis in plasma cell differentiation | Q34345459 | ||
Dissecting glycoprotein quality control in the secretory pathway | Q34394333 | ||
IRE1: a role in UPREgulation of ER degradation | Q35065944 | ||
The contribution of N-glycans and their processing in the endoplasmic reticulum to glycoprotein biosynthesis | Q35123504 | ||
Quality Control and Protein Folding in the Secretory Pathway | Q35564863 | ||
Calnexin, calreticulin, and ERp57: teammates in glycoprotein folding | Q35625698 | ||
Sequential assistance of molecular chaperones and transient formation of covalent complexes during protein degradation from the ER. | Q36323835 | ||
Transport of protein between cytoplasmic membranes of fused cells: correspondence to processes reconstituted in a cell-free system | Q36510371 | ||
Enhancement of endoplasmic reticulum (ER) degradation of misfolded Null Hong Kong alpha1-antitrypsin by human ER mannosidase I. | Q38354843 | ||
Cystic fibrosis transmembrane conductance regulator degradation depends on the lectins Htm1p/EDEM and the Cdc48 protein complex in yeast | Q39968686 | ||
Quality control by proteases in the endoplasmic reticulum. Removal of a protease-sensitive site enhances expression of human P-glycoprotein. | Q40992489 | ||
Detecting and measuring cotranslational protein degradation in vivo | Q44397626 | ||
Cotranslational ubiquitination of cystic fibrosis transmembrane conductance regulator in vitro | Q46929811 | ||
In situ hybridization studies suggest a role for the basic region‐leucine zipper protein hXBP‐1 in exocrine gland and skeletal development during mouse embryogenesis | Q52224944 | ||
EDEM contributes to maintenance of protein folding efficiency and secretory capacity. | Q54352454 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | endoplasmic reticulum | Q79927 |
P304 | page(s) | 2424-2428 | |
P577 | publication date | 2004-12-03 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | A novel stress-induced EDEM variant regulating endoplasmic reticulum-associated glycoprotein degradation | |
P478 | volume | 280 |
Q27935416 | A Complex of Htm1 and the Oxidoreductase Pdi1 Accelerates Degradation of Misfolded Glycoproteins |
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Q42703690 | A new autophagy-related checkpoint in the degradation of an ERAD-M target |
Q35354864 | A review of the mammalian unfolded protein response. |
Q87927693 | Abnormal expression of ER quality control and ER associated degradation proteins in the dorsolateral prefrontal cortex in schizophrenia |
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Q33353825 | Phylogenetic analyses suggest multiple changes of substrate specificity within the glycosyl hydrolase 20 family |
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