about
ADP-ribosylation factor/COPI-dependent events at the endoplasmic reticulum-Golgi interface are regulated by the guanine nucleotide exchange factor GBF1The cargo receptors Surf4, endoplasmic reticulum-Golgi intermediate compartment (ERGIC)-53, and p25 are required to maintain the architecture of ERGIC and Golgi.GS15 forms a SNARE complex with syntaxin 5, GS28, and Ykt6 and is implicated in traffic in the early cisternae of the Golgi apparatus.Diacylglycerol kinase delta suppresses ER-to-Golgi traffic via its SAM and PH domainsMaintenance of Golgi structure and function depends on the integrity of ER exportNudel functions in membrane traffic mainly through association with Lis1 and cytoplasmic dyneinA novel imaging method for quantitative Golgi localization reveals differential intra-Golgi trafficking of secretory cargoes.Cellular COPII proteins are involved in production of the vesicles that form the poliovirus replication complex.Structural basis for the cooperative interplay between the two causative gene products of combined factor V and factor VIII deficiencyStructural Characterization of Carbohydrate Binding by LMAN1 Protein Provides New Insight into the Endoplasmic Reticulum Export of Factors V (FV) and VIII (FVIII)Structural Basis for Disparate Sugar-Binding Specificities in the Homologous Cargo Receptors ERGIC-53 and VIP36Lst1p and Sec24p cooperate in sorting of the plasma membrane ATPase into COPII vesicles in Saccharomyces cerevisiae.Arms Race between Enveloped Viruses and the Host ERAD MachinerySecretory bulk flow of soluble proteins is efficient and COPII dependentLocalization of p24 putative cargo receptors in the early secretory pathway depends on the biosynthetic activity of the cellRab1 defines a novel pathway connecting the pre-Golgi intermediate compartment with the cell periphery.Immunolocalization of UDP-glucose:glycoprotein glucosyltransferase indicates involvement of pre-Golgi intermediates in protein quality controlDynamics of transitional endoplasmic reticulum sites in vertebrate cellsProtein interaction profiling of the p97 adaptor UBXD1 points to a role for the complex in modulating ERGIC-53 trafficking.Human cytomegalovirus UL99-encoded pp28 is required for the cytoplasmic envelopment of tegument-associated capsids.Intracellular phospholipase A1gamma (iPLA1gamma) is a novel factor involved in coat protein complex I- and Rab6-independent retrograde transport between the endoplasmic reticulum and the Golgi complexQuantitative ER <--> Golgi transport kinetics and protein separation upon Golgi exit revealed by vesicular integral membrane protein 36 dynamics in live cells.Glycosyltransferase-specific Golgi-targeting mechanisms.Topology of molecular machines of the endoplasmic reticulum: a compilation of proteomics and cytological data.Endoplasmic reticulum export sites and Golgi bodies behave as single mobile secretory units in plant cells.Identification of ERGIC-53 as an intracellular transport receptor of alpha1-antitrypsin.EF-hand domains of MCFD2 mediate interactions with both LMAN1 and coagulation factor V or VIII.Carbohydrate- and conformation-dependent cargo capture for ER-exitFollowing the fate in vivo of COPI vesicles generated in vitro.Isoform-selective effects of the depletion of ADP-ribosylation factors 1-5 on membrane trafficActivation of mammalian unfolded protein response is compatible with the quality control system operating in the endoplasmic reticulumPhosphatidylinositol 3-kinase and COPII generate LC3 lipidation vesicles from the ER-Golgi intermediate compartment.Molecular basis of LMAN1 in coordinating LMAN1-MCFD2 cargo receptor formation and ER-to-Golgi transport of FV/FVIIIDissecting rotavirus particle-raft interaction with small interfering RNAs: insights into rotavirus transit through the secretory pathway.Syntaxin 1A regulates surface expression of beta-cell ATP-sensitive potassium channels.Modulating endoplasmic reticulum-Golgi cargo receptors for improving secretion of carrier-fused heterologous proteins in the filamentous fungus Aspergillus oryzae.A novel fluorescence-based biosynthetic trafficking method provides pharmacologic evidence that PI4-kinase IIIα is important for protein trafficking from the endoplasmic reticulum to the plasma membraneIdentification of a small molecule activator of novel PKCs for promoting glucose-dependent insulin secretion.The Golgi apparatus maintains its organization independent of the endoplasmic reticulum.Androgen-regulated formation and degradation of gap junctions in androgen-responsive human prostate cancer cells
P2860
Q24305198-885194A9-DEF2-49A5-BDD8-2FD21BD8E2E3Q24315827-78B8E3EC-68C4-4CC6-9352-71474567C1E9Q24537246-0F35C9F8-4B7F-44D5-B201-038B0C81B4E4Q24555039-588CA4FC-1DAA-407B-B211-59208B126F48Q24653507-666A072E-DB33-4EF3-A4B5-D0567D03ECC2Q24678185-3BDE9ACD-911F-49E7-A592-A2CE45EF7F7EQ27304993-81499E55-B6A5-4ABA-BD0E-093161854B98Q27469873-F925EF93-0468-43B8-BB80-AF6CF0F45133Q27659667-3B42BA35-3D9F-409F-B84C-7B02A33353EBQ27678322-D837CBE5-0097-48BF-BC92-ADED093C941FQ27681589-048E81EF-CEA2-400C-8F71-4862005278DCQ27939936-61070910-B571-470A-9630-DF34D0CA7642Q28078319-A5110AC7-5071-4E08-B402-B3210886CFDAQ28350951-1AB3B435-6623-45B0-B930-1262EFEED05DQ28364638-FF5E592F-66CF-4D3B-A278-97B8ABFB62F6Q28572875-5C7F0018-5C0B-49FC-BBAD-07248F94E008Q28582340-6C61F4F3-41E9-4A4B-AE09-FD24A92EC9D6Q28645796-46F479AB-CC64-4FE7-805F-67342DE4AF20Q30274646-9934DBF6-2A6E-4E42-9A3D-741633D8E59CQ30333473-CE8C4501-0741-4CE3-9FA9-DE079A703AA2Q30492044-83936242-CA9F-4F22-8554-7895D7118743Q30525331-ABCB7295-A481-4B72-9B41-61E7F145D124Q30527898-AB11E898-AC4E-4E18-937B-02E025D2BA5DQ31141736-0DCF09DD-5430-475A-9147-292E4DDD8592Q33203998-5DD238C0-EDAC-4CC2-914C-B2D996F057A1Q33320261-CEE13D77-7D08-4F7D-8628-061EA5625CA0Q33634437-375C0DBA-861C-4458-9A66-E9C0C0295965Q33913865-1CBB6FB5-A21A-4E1E-AB29-94A1E274085EQ34016461-09B4F9CD-EE46-4BC3-AF20-ACA82A6AFFCCQ34049667-3862DDF6-8712-4FA0-B4CC-20C3CE8F182EQ34358672-8E2E52BB-2AED-4131-9E66-98EEC338DB87Q34450023-3E33C098-FFB0-408B-A70B-70699D2CFB4AQ34541760-6F6601D0-6297-49A4-A147-DDAC506CDF0DQ34545950-FEFE6A50-C27D-459A-968E-44A67BE9D178Q34718049-13556BED-A204-4B4F-B154-12B94FF69CFCQ34777618-50316CA9-6963-4BA3-B9E0-B1FD9767F242Q35163837-3F4DE332-047B-4215-A75D-A9B2DEDCDA05Q35187794-F2ABDC67-B510-4D44-9451-7283EE12DE82Q35191029-0B4E8FE7-AE17-4172-B583-581BEB3207F1Q35191051-60A24C59-4757-4AFC-B9F9-93535C89D51A
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
ERGIC-53 and traffic in the secretory pathway
@ast
ERGIC-53 and traffic in the secretory pathway
@en
ERGIC-53 and traffic in the secretory pathway
@nl
type
label
ERGIC-53 and traffic in the secretory pathway
@ast
ERGIC-53 and traffic in the secretory pathway
@en
ERGIC-53 and traffic in the secretory pathway
@nl
prefLabel
ERGIC-53 and traffic in the secretory pathway
@ast
ERGIC-53 and traffic in the secretory pathway
@en
ERGIC-53 and traffic in the secretory pathway
@nl
P2093
P3181
P1476
ERGIC-53 and traffic in the secretory pathway
@en
P2093
Andersson H
Appenzeller C
Kappeler F
P304
P3181
P407
P478
113 ( Pt 4)
P577
2000-02-01T00:00:00Z