scholarly article | Q13442814 |
P819 | ADS bibcode | 2014PNAS..111E.582S |
P356 | DOI | 10.1073/PNAS.1318114111 |
P8608 | Fatcat ID | release_rlacamhyrvezhlk5hbbzsktuce |
P932 | PMC publication ID | 3918815 |
P698 | PubMed publication ID | 24453213 |
P5875 | ResearchGate publication ID | 259878163 |
P50 | author | Ling Qi | Q37375214 |
Shengyi Sun | Q37829359 | ||
Sander Kersten | Q38320639 | ||
Jason W. Locasale | Q41047918 | ||
Qiaoming Long | Q43194579 | ||
Guojun Shi | Q56395873 | ||
Nuno Mendonça | Q58613047 | ||
Adam B Francisco | Q83104820 | ||
P2093 | author name string | Kenneth W Simpson | |
John R Yates | |||
Xuemei Han | |||
Xiaojing Liu | |||
Yewei Ji | |||
Gerald E Duhamel | |||
P2860 | cites work | A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery | Q21092417 |
A conditional knockout resource for the genome-wide study of mouse gene function | Q21735918 | ||
Defining human ERAD networks through an integrative mapping strategy | Q24298439 | ||
SEL1L protein critically determines the stability of the HRD1-SEL1L endoplasmic reticulum-associated degradation (ERAD) complex to optimize the degradation kinetics of ERAD substrates | Q24298501 | ||
A ubiquitin ligase-associated chaperone holdase maintains polypeptides in soluble states for proteasome degradation | Q24305231 | ||
OS-9 and GRP94 deliver mutant alpha1-antitrypsin to the Hrd1-SEL1L ubiquitin ligase complex for ERAD | Q24312778 | ||
Human OS-9, a lectin required for glycoprotein endoplasmic reticulum-associated degradation, recognizes mannose-trimmed N-glycans | Q24313146 | ||
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 | ||
Multiprotein complexes that link dislocation, ubiquitination, and extraction of misfolded proteins from the endoplasmic reticulum membrane | Q24530318 | ||
A luminal surveillance complex that selects misfolded glycoproteins for ER-associated degradation | Q27930372 | ||
A regulatory link between ER-associated protein degradation and the unfolded-protein response | Q27931238 | ||
Distinct ubiquitin-ligase complexes define convergent pathways for the degradation of ER proteins | Q27931299 | ||
Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradation | Q28131669 | ||
Protein misfolding, functional amyloid, and human disease | Q28131732 | ||
EDEM as an acceptor of terminally misfolded glycoproteins released from calnexin | Q28212764 | ||
Regulation of hepatic lipogenesis by the transcription factor XBP1 | Q28507784 | ||
XBP-1 is required for biogenesis of cellular secretory machinery of exocrine glands | Q28510479 | ||
Deficiency of suppressor enhancer Lin12 1 like (SEL1L) in mice leads to systemic endoplasmic reticulum stress and embryonic lethality | Q28587457 | ||
Essential role of synoviolin in embryogenesis | Q28588247 | ||
Global survey of organ and organelle protein expression in mouse: combined proteomic and transcriptomic profiling | Q28588350 | ||
Derlin-2-deficient mice reveal an essential role for protein dislocation in chondrocytes | Q28593497 | ||
Diabetes mellitus and exocrine pancreatic dysfunction in perk-/- mice reveals a role for translational control in secretory cell survival | Q28593963 | ||
Suppressors of a lin-12 hypomorph define genes that interact with both lin-12 and glp-1 in Caenorhabditis elegans | Q28623285 | ||
Derlin-1 deficiency is embryonic lethal, Derlin-3 deficiency appears normal, and Herp deficiency is intolerant to glucose load and ischemia in mice | Q28730861 | ||
The unfolded protein response: from stress pathway to homeostatic regulation | Q29547396 | ||
The unfolded protein response: controlling cell fate decisions under ER stress and beyond | Q29615499 | ||
Eukaryotic stress granules: the ins and outs of translation | Q29619569 | ||
Autophagy counterbalances endoplasmic reticulum expansion during the unfolded protein response | Q33264844 | ||
SEL1L deficiency impairs growth and differentiation of pancreatic epithelial cells | Q33532789 | ||
Grp78 heterozygosity promotes adaptive unfolded protein response and attenuates diet-induced obesity and insulin resistance | Q33556664 | ||
Stringent requirement for HRD1, SEL1L, and OS-9/XTP3-B for disposal of ERAD-LS substrates | Q33615098 | ||
A Phos-tag-based approach reveals the extent of physiological endoplasmic reticulum stress | Q33641274 | ||
IRE1α Disruption Causes Histological Abnormality of Exocrine Tissues, Increase of Blood Glucose Level, and Decrease of Serum Immunoglobulin Level | Q33707431 | ||
The Caenorhabditis elegans sel-1 gene, a negative regulator of lin-12 and glp-1, encodes a predicted extracellular protein. | Q33967319 | ||
SEL1L a multifaceted protein playing a role in tumor progression. | Q34473389 | ||
A novel polymorphism in SEL1L confers susceptibility to Alzheimer's disease | Q34484551 | ||
Processing and turnover of the Hedgehog protein in the endoplasmic reticulum | Q34637854 | ||
Endoplasmic reticulum stress triggers autophagy | Q35690087 | ||
The ATP-P2X7 signaling axis is dispensable for obesity-associated inflammasome activation in adipose tissue | Q35976791 | ||
SEL1L, the homologue of yeast Hrd3p, is involved in protein dislocation from the mammalian ER. | Q36119119 | ||
Endoplasmic reticulum degradation requires lumen to cytosol signaling. Transmembrane control of Hrd1p by Hrd3p. | Q36358009 | ||
Cleaning up: ER-associated degradation to the rescue | Q36464919 | ||
Unassembled CD147 is an endogenous endoplasmic reticulum-associated degradation substrate | Q36465057 | ||
Nonmuscle myosin IIB links cytoskeleton to IRE1α signaling during ER stress. | Q36540356 | ||
ER stress potentiates insulin resistance through PERK-mediated FOXO phosphorylation | Q36660203 | ||
The ERdj5-Sel1L complex facilitates cholera toxin retrotranslocation | Q36680557 | ||
SEL1L nucleates a protein complex required for dislocation of misfolded glycoproteins | Q36858538 | ||
Purinergic receptors in the endocrine and exocrine pancreas. | Q37119875 | ||
The mammalian endoplasmic reticulum-associated degradation system | Q37122324 | ||
The unfolded protein response transducer ATF6 represents a novel transmembrane-type endoplasmic reticulum-associated degradation substrate requiring both mannose trimming and SEL1L protein | Q37272082 | ||
Role of 26S proteasome and HRD genes in the degradation of 3-hydroxy-3-methylglutaryl-CoA reductase, an integral endoplasmic reticulum membrane protein | Q37383994 | ||
Synthesis, intracellular transport and discharge of exportable proteins in the pancreatic acinar cell and other cells | Q37792053 | ||
Finding the will and the way of ERAD substrate retrotranslocation | Q38031342 | ||
Stress granules and cell signaling: more than just a passing phase? | Q38136844 | ||
Unravelling the ultrastructure of stress granules and associated P-bodies in human cells. | Q39297506 | ||
mSEL-1L (Suppressor/enhancer Lin12-like) protein levels influence murine neural stem cell self-renewal and lineage commitment | Q39567184 | ||
The IRE1alpha-XBP1 pathway of the unfolded protein response is required for adipogenesis | Q39843795 | ||
SEL1L and HRD1 are involved in the degradation of unassembled secretory Ig-mu chains | Q40006668 | ||
Exocrine pancreatic insufficiency | Q40912160 | ||
Possible involvement of phosphorylation of occludin in tight junction formation | Q41104367 | ||
Role of the SEL1L:LC3-I complex as an ERAD tuning receptor in the mammalian ER. | Q44455557 | ||
SEL1L microsatellite polymorphism in Japanese patients with autoimmune thyroid diseases | Q73875542 | ||
Degradation of misfolded proteins prevents ER-derived oxidative stress and cell death | Q80531680 | ||
P2507 | corrigendum / erratum | Correction for Sun et al., Sel1L is indispensable for mammalian endoplasmic reticulum-associated degradation, endoplasmic reticulum homeostasis, and survival | Q61919925 |
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | endoplasmic reticulum | Q79927 |
P304 | page(s) | E582-91 | |
P577 | publication date | 2014-01-22 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Sel1L is indispensable for mammalian endoplasmic reticulum-associated degradation, endoplasmic reticulum homeostasis, and survival | |
P478 | volume | 111 |
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Q35859583 | Epithelial Sel1L is required for the maintenance of intestinal homeostasis |
Q36581422 | Familial prion protein mutants inhibit Hrd1-mediated retrotranslocation of misfolded proteins by depleting misfolded protein sensor BiP. |
Q40013365 | Genome-wide association study in mice identifies loci affecting liver-related phenotypes including Sel1l influencing serum bile acids |
Q58616116 | Hepatic Sel1L-Hrd1 ER-associated degradation (ERAD) manages FGF21 levels and systemic metabolism via CREBH |
Q46238616 | High capacity of the endoplasmic reticulum to prevent secretion and aggregation of amyloidogenic proteins. |
Q92538101 | Host Gene SEL1L Involved in Endoplasmic Reticulum-Associated Degradation Pathway Could Inhibit Hepatitis B Virus at RNA, DNA, and Protein Levels |
Q49851092 | Hypothalamic ER-associated degradation regulates POMC maturation, feeding, and age-associated obesity. |
Q36348190 | IRE1α is an endogenous substrate of endoplasmic-reticulum-associated degradation |
Q36716367 | Inhibition of the FKBP family of peptidyl prolyl isomerases induces abortive translocation and degradation of the cellular prion protein |
Q48330630 | Melatonin reduces endoplasmic reticulum stress and corneal dystrophy-associated TGFBIp through activation of endoplasmic reticulum-associated protein degradation. |
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