| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Ludwig Eichinger | Q60849131 |
| P2093 | author name string | Wenjing Li | |
| Changxin Wu | |||
| Ping Li | |||
| Min Yang | |||
| Qiuhong Xiong | |||
| P2860 | cites work | The plasma membrane brings autophagosomes to life | Q57082945 |
| The ATG5-binding and coiled coil domains of ATG16L1 maintain autophagy and tissue homeostasis in mice independently of the WD domain required for LC3-associated phagocytosis | Q58592514 | ||
| An ATG16L1-dependent pathway promotes plasma membrane repair and limits Listeria monocytogenes cell-to-cell spread | Q60222378 | ||
| Macroautophagy is required for multicellular development of the social amoeba Dictyostelium discoideum | Q73100649 | ||
| Crohn's disease-associated ATG16L1 polymorphism modulates pro-inflammatory cytokine responses selectively upon activation of NOD2 | Q83619372 | ||
| ATG16L1 polymorphisms are associated with NOD2-induced hyperinflammation | Q84361988 | ||
| ATG16L1 contributes to Crohn's disease susceptibility in Koreans: overmuch concern for ethnic difference? | Q85273629 | ||
| ATG5 is required for B cell polarization and presentation of particulate antigens | Q91344147 | ||
| α-Synuclein Is Degraded by Both Autophagy and the Proteasome | Q44420467 | ||
| LC3-Associated Phagocytosis Is Required for Dendritic Cell Inflammatory Cytokine Response to Gut Commensal Yeast Saccharomyces cerevisiae. | Q47116608 | ||
| Molecular control of chaperone-mediated autophagy | Q47301133 | ||
| The mammalian ULK1 complex and autophagy initiation. | Q47301180 | ||
| Autophagic clearance of proteasomes in yeast requires the conserved sorting nexin Snx4. | Q47434242 | ||
| The WD40 domain of ATG16L1 is required for its non-canonical role in lipidation of LC3 at single membranes. | Q47556315 | ||
| Drosophila Atg16 promotes enteroendocrine cell differentiation via regulation of intestinal Slit/Robo signaling | Q47690721 | ||
| Involvement of macroautophagy in the dissolution of neuronal inclusions. | Q50788486 | ||
| Degradation of proteasomes by lysosomes in rat liver. | Q51590715 | ||
| Loss of Dictyostelium ATG9 results in a pleiotropic phenotype affecting growth, development, phagocytosis and clearance and replication of Legionella pneumophila. | Q51918047 | ||
| Dictyostelium macroautophagy mutants vary in the severity of their developmental defects. | Q52094720 | ||
| Crosstalk between lysine methylation and phosphorylation of ATG16L1 dictates the apoptosis of hypoxia/reoxygenation-induced cardiomyocytes. | Q52596603 | ||
| Autophagy-related gene16L2, a potential serum biomarker of multiple sclerosis evaluated by bead-based proteomic technology. | Q54228403 | ||
| Staphylococcus aureusSubvert Autophagy for Induction of Caspase-independent Host Cell Death | Q56777113 | ||
| ATG16 mediates the autophagic degradation of the 19S proteasomal subunits PSMD1 and PSMD2 | Q57074349 | ||
| Rab33b and Rab6 are functionally overlapping regulators of Golgi homeostasis and trafficking | Q24299808 | ||
| Sequestosome 1/p62 shuttles polyubiquitinated tau for proteasomal degradation | Q24305254 | ||
| TMEM59 defines a novel ATG16L1-binding motif that promotes local activation of LC3 | Q24313405 | ||
| FIP200 regulates targeting of Atg16L1 to the isolation membrane | Q24314938 | ||
| Cloning and analysis of human Apg16L | Q24336706 | ||
| Golgi-resident small GTPase Rab33B interacts with Atg16L and modulates autophagosome formation | Q24336821 | ||
| TRIM-mediated precision autophagy targets cytoplasmic regulators of innate immunity | Q24338801 | ||
| The pre-autophagosomal structure organized by concerted functions of APG genes is essential for autophagosome formation | Q24535862 | ||
| Mammalian autophagy: core molecular machinery and signaling regulation | Q24595447 | ||
| The Atg16L complex specifies the site of LC3 lipidation for membrane biogenesis in autophagy | Q24647053 | ||
| Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis | Q24656576 | ||
| WD40 Repeat Propellers Define a Ubiquitin-Binding Domain that Regulates Turnover of F Box Proteins | Q27665843 | ||
| Insights into autophagosome maturation revealed by the structures of ATG5 with its interacting partners | Q27696515 | ||
| Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease | Q27860821 | ||
| The Atg12-Atg5 conjugate has a novel E3-like activity for protein lipidation in autophagy | Q27933717 | ||
| Formation of the approximately 350-kDa Apg12-Apg5.Apg16 multimeric complex, mediated by Apg16 oligomerization, is essential for autophagy in yeast | Q27934020 | ||
| Apg16p is required for the function of the Apg12p-Apg5p conjugate in the yeast autophagy pathway | Q27936903 | ||
| Mechanism and functions of membrane binding by the Atg5-Atg12/Atg16 complex during autophagosome formation | Q27939934 | ||
| Two distinct Vps34 phosphatidylinositol 3-kinase complexes function in autophagy and carboxypeptidase Y sorting in Saccharomyces cerevisiae | Q27940050 | ||
| TipC and the chorea-acanthocytosis protein VPS13A regulate autophagy in Dictyostelium and human HeLa cells | Q28118371 | ||
| The WD repeat: a common architecture for diverse functions | Q28143827 | ||
| Mouse Apg16L, a novel WD-repeat protein, targets to the autophagic isolation membrane with the Apg12-Apg5 conjugate | Q28187453 | ||
| Identification of rabaptin-5, rabex-5, and GM130 as putative effectors of rab33b, a regulator of retrograde traffic between the Golgi apparatus and ER | Q28206641 | ||
| The ancient regulatory-protein family of WD-repeat proteins | Q28248516 | ||
| Selective autophagy mediated by autophagic adapter proteins | Q28301940 | ||
| HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS | Q28306195 | ||
| Autophagic Degradation of the 26S Proteasome Is Mediated by the Dual ATG8/Ubiquitin Receptor RPN10 in Arabidopsis | Q28830597 | ||
| Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations | Q28943541 | ||
| Autophagosome formation: core machinery and adaptations | Q29547417 | ||
| Loss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1beta production | Q29614472 | ||
| Toll-like receptor signalling in macrophages links the autophagy pathway to phagocytosis | Q29614481 | ||
| Plasma membrane contributes to the formation of pre-autophagosomal structures | Q29614494 | ||
| A role for ubiquitin in selective autophagy | Q29614499 | ||
| A key role for autophagy and the autophagy gene Atg16l1 in mouse and human intestinal Paneth cells | Q29614565 | ||
| A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 | Q29614873 | ||
| Nod1 and Nod2 direct autophagy by recruiting ATG16L1 to the plasma membrane at the site of bacterial entry | Q29615618 | ||
| Aggregate-prone proteins with polyglutamine and polyalanine expansions are degraded by autophagy | Q29622819 | ||
| Ubiquitin and ubiquitin-like proteins as multifunctional signals | Q30014838 | ||
| WIPI2 links LC3 conjugation with PI3P, autophagosome formation, and pathogen clearance by recruiting Atg12-5-16L1. | Q30090184 | ||
| Connexins modulate autophagosome biogenesis | Q30577497 | ||
| Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant | Q33375721 | ||
| The two C. elegans ATG-16 homologs have partially redundant functions in the basal autophagy pathway | Q33638704 | ||
| C. elegans screen identifies autophagy genes specific to multicellular organisms | Q34120920 | ||
| Diverse autophagosome membrane sources coalesce in recycling endosomes. | Q34370963 | ||
| Biological basket weaving: formation and function of clathrin-coated vesicles | Q34425195 | ||
| Heteromeric p97/p97R155C complexes induce dominant negative changes in wild-type and autophagy 9-deficient Dictyostelium strains | Q34442393 | ||
| The multifaceted Paneth cell | Q34531936 | ||
| Annexin A2 promotes phagophore assembly by enhancing Atg16L⁺ vesicle biogenesis and homotypic fusion | Q34988358 | ||
| Autophagy suppresses interleukin-1β (IL-1β) signaling by activation of p62 degradation via lysosomal and proteasomal pathways. | Q35763237 | ||
| Linking of autophagy to ubiquitin-proteasome system is important for the regulation of endoplasmic reticulum stress and cell viability | Q35916071 | ||
| Connexins: substrates and regulators of autophagy | Q36031118 | ||
| Atg16L1 deficiency confers protection from uropathogenic Escherichia coli infection in vivo | Q36079542 | ||
| ATG16L1 phosphorylation is oppositely regulated by CSNK2/casein kinase 2 and PPP1/protein phosphatase 1 which determines the fate of cardiomyocytes during hypoxia/reoxygenation | Q36111818 | ||
| Atg16L1, an essential factor for canonical autophagy, participates in hormone secretion from PC12 cells independently of autophagic activity. | Q36161685 | ||
| Molecular characterization of LC3-associated phagocytosis reveals distinct roles for Rubicon, NOX2 and autophagy proteins | Q36181466 | ||
| Starvation Induces Proteasome Autophagy with Different Pathways for Core and Regulatory Particles. | Q36573940 | ||
| Interaction between FIP200 and ATG16L1 distinguishes ULK1 complex-dependent and -independent autophagy. | Q36589045 | ||
| Ubiquitin receptors and protein quality control | Q36606405 | ||
| Ubiquitin regulates caspase recruitment domain-mediated signaling by nucleotide-binding oligomerization domain-containing proteins NOD1 and NOD2. | Q36666117 | ||
| Three isoforms of the Atg16L1 protein contribute different autophagic properties | Q36791743 | ||
| The Crohn's disease: associated ATG16L1 variant and Salmonella invasion | Q36939162 | ||
| The T300A Crohn's disease risk polymorphism impairs function of the WD40 domain of ATG16L1. | Q36986458 | ||
| Recruitment of the autophagic machinery to endosomes during infection is mediated by ubiquitin. | Q37233581 | ||
| TMEM166/EVA1A interacts with ATG16L1 and induces autophagosome formation and cell death | Q37412484 | ||
| p62- and ubiquitin-dependent stress-induced autophagy of the mammalian 26S proteasome. | Q37451072 | ||
| Molecular basis of canonical and bactericidal autophagy | Q37593770 | ||
| Mechanisms of cross-talk between the ubiquitin-proteasome and autophagy-lysosome systems | Q37664227 | ||
| Regulation of mammalian autophagy in physiology and pathophysiology. | Q37801517 | ||
| Involvement of members of the Rab family and related small GTPases in autophagosome formation and maturation | Q37891848 | ||
| Substrate recognition in selective autophagy and the ubiquitin-proteasome system. | Q38094868 | ||
| Biology and trafficking of ATG9 and ATG16L1, two proteins that regulate autophagosome formation | Q38106561 | ||
| Historical landmarks of autophagy research | Q38173674 | ||
| Autophagy in Dictyostelium: Mechanisms, regulation and disease in a simple biomedical model. | Q38813809 | ||
| A Crohn's disease variant in Atg16l1 enhances its degradation by caspase 3. | Q39022431 | ||
| A novel crosstalk between two major protein degradation systems: regulation of proteasomal activity by autophagy. | Q39112279 | ||
| Fine-tuning of ULK1 mRNA and protein levels is required for autophagy oscillation. | Q39312592 | ||
| The Logic of the 26S Proteasome | Q39318404 | ||
| ATG16L1 meets ATG9 in recycling endosomes: additional roles for the plasma membrane and endocytosis in autophagosome biogenesis. | Q39394984 | ||
| Crohn's disease-associated adherent-invasive E. coli are selectively favoured by impaired autophagy to replicate intracellularly | Q39800747 | ||
| Inhibition of lysosomal functions reduces proteasomal activity | Q39853835 | ||
| Autophagy inhibition compromises degradation of ubiquitin-proteasome pathway substrates. | Q39878605 | ||
| Lysosomal enzyme cathepsin D protects against alpha-synuclein aggregation and toxicity | Q39914071 | ||
| Direct link between Atg protein and small GTPase Rab: Atg16L functions as a potential Rab33 effector in mammals | Q40064387 | ||
| The phenotypes of ATG9, ATG16 and ATG9/16 knock-out mutants imply autophagy-dependent and -independent functions | Q40352767 | ||
| Loss of Atg16 delays the alcohol-induced sedation response via regulation of Corazonin neuropeptide production in Drosophila | Q40515563 | ||
| ATG16L1 and pathogenesis of urinary tract infections | Q41276663 | ||
| tip genes act in parallel pathways of early Dictyostelium development | Q41678638 | ||
| Differential involvement of Atg16L1 in Crohn disease and canonical autophagy: analysis of the organization of the Atg16L1 complex in fibroblasts | Q41833476 | ||
| Atg16L2, a novel isoform of mammalian Atg16L that is not essential for canonical autophagy despite forming an Atg12–5-16L2 complex | Q41879755 | ||
| Atg16l1 is required for autophagy in intestinal epithelial cells and protection of mice from Salmonella infection | Q41882233 | ||
| It's all about talking: two-way communication between proteasomal and lysosomal degradation pathways via ubiquitin | Q42361268 | ||
| Plasma membrane helps autophagosomes grow | Q42606019 | ||
| Dimeric coiled-coil structure of Saccharomyces cerevisiae Atg16 and its functional significance in autophagy | Q42943842 | ||
| Processing of autophagic protein LC3 by the 20S proteasome | Q43198342 | ||
| P275 | copyright license | Creative Commons Attribution | Q6905323 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P921 | main subject | proteasome endopeptidase complex | Q13107625 |
| autophagy | Q288322 | ||
| P577 | publication date | 2018-12-20 | |
| P1433 | published in | Cells | Q27724621 |
| P1476 | title | The Role of ATG16 in Autophagy and The Ubiquitin Proteasome System | |
| P478 | volume | 8 |
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