| scholarly article | Q13442814 |
| P2093 | author name string | R. H. Scheller | |
| D. S. Chao | |||
| C. S. Kuo | |||
| J. C. Hay | |||
| P2860 | cites work | The BOS1 gene encodes an essential 27-kD putative membrane protein that is required for vesicular transport from the ER to the Golgi complex in yeast | Q36529463 |
| A mammalian homologue of SLY1, a yeast gene required for transport from endoplasmic reticulum to Golgi | Q48065616 | ||
| Ypt1p implicated in v-SNARE activation | Q59095937 | ||
| N-Ethylmaleimide-sensitive factor acts at a prefusion ATP-dependent step in Ca2+-activated exocytosis | Q71246062 | ||
| The syntaxin family of vesicular transport receptors | Q24310598 | ||
| A v-SNARE implicated in intra-Golgi transport | Q24312623 | ||
| Mammalian vesicle trafficking proteins of the endoplasmic reticulum and Golgi apparatus | Q24336661 | ||
| SED5 encodes a 39-kD integral membrane protein required for vesicular transport between the ER and the Golgi complex | Q27938084 | ||
| Bos1p, an integral membrane protein of the endoplasmic reticulum to Golgi transport vesicles, is required for their fusion competence | Q27939021 | ||
| Identification and structure of four yeast genes (SLY) that are able to suppress the functional loss of YPT1, a member of the RAS superfamily | Q27939653 | ||
| SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
| Specificity and regulation of a synaptic vesicle docking complex | Q28246613 | ||
| A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion | Q28255534 | ||
| The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression | Q28277156 | ||
| A new syntaxin family member implicated in targeting of intracellular transport vesicles | Q28282159 | ||
| Mammalian Sly1 regulates syntaxin 5 function in endoplasmic reticulum to Golgi transport | Q28569244 | ||
| GS28, a 28-kilodalton Golgi SNARE that participates in ER-Golgi transport | Q28580207 | ||
| Sec18p (NSF)-driven release of Sec17p (alpha-SNAP) can precede docking and fusion of yeast vacuoles | Q28609819 | ||
| A rab protein is required for the assembly of SNARE complexes in the docking of transport vesicles | Q29620271 | ||
| rSec6 and rSec8, mammalian homologs of yeast proteins essential for secretion | Q33857254 | ||
| The molecular machinery for secretion is conserved from yeast to neurons | Q36184412 | ||
| Characteristics of endoplasmic reticulum-derived transport vesicles | Q36234617 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Golgi apparatus | Q83181 |
| endoplasmic reticulum | Q79927 | ||
| Calnexin | Q14876769 | ||
| Bet1 golgi vesicular membrane trafficking protein | Q21982781 | ||
| Golgi SNAP receptor complex member 2 | Q21984859 | ||
| SEC22 homolog B, vesicle trafficking protein | Q21991103 | ||
| Syntaxin 5A | Q21991750 | ||
| P304 | page(s) | 149–158 | |
| P577 | publication date | 1997-04-04 | |
| P1433 | published in | Cell | Q655814 |
| P1476 | title | Protein interactions regulating vesicle transport between the endoplasmic reticulum and Golgi apparatus in mammalian cells | |
| P478 | volume | 89 |
| Q47682122 | A 29-kilodalton Golgi soluble N-ethylmaleimide-sensitive factor attachment protein receptor (Vti1-rp2) implicated in protein trafficking in the secretory pathway |
| Q24322596 | A SNARE involved in protein transport through the Golgi apparatus |
| Q37086983 | A genomic comparison of in vivo and in vitro brain microvascular endothelial cells |
| Q27631238 | A novel snare N-terminal domain revealed by the crystal structure of Sec22b |
| Q24310308 | A novel synaptobrevin/VAMP homologous protein (VAMP5) is increased during in vitro myogenesis and present in the plasma membrane |
| Q27930001 | A role for Tlg1p in the transport of proteins within the Golgi apparatus of Saccharomyces cerevisiae |
| Q33959206 | A systematic screen for tube morphogenesis and branching genes in the Drosophila tracheal system. |
| Q92642062 | A trap mutant reveals the physiological client spectrum of TRC40 |
| Q42674921 | APP-BP1 inhibits Abeta42 levels by interacting with Presenilin-1. |
| Q28570066 | An isoform of the Golgi t-SNARE, syntaxin 5, with an endoplasmic reticulum retrieval signal |
| Q37244865 | Anterograde flow of cargo across the golgi stack potentially mediated via bidirectional "percolating" COPI vesicles |
| Q51892011 | Arabidopsis SNARE protein SEC22 is essential for gametophyte development and maintenance of Golgi-stack integrity. |
| Q33869794 | Arrangement of subunits in 20 S particles consisting of NSF, SNAPs, and SNARE complexes. |
| Q24291274 | Association of a novel PDZ domain-containing peripheral Golgi protein with the Q-SNARE (Q-soluble N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein receptor) protein syntaxin 6 |
| Q27932451 | Asymmetric requirements for a Rab GTPase and SNARE proteins in fusion of COPII vesicles with acceptor membranes |
| Q24337387 | Autophagic substrate clearance requires activity of the syntaxin-5 SNARE complex |
| Q24598772 | B cells promote insulin resistance through modulation of T cells and production of pathogenic IgG antibodies |
| Q50296303 | BET1:GOSR2:STX5 bind v-SNARES on tethered vesicle |
| Q24537148 | CASP, the alternatively spliced product of the gene encoding the CCAAT-displacement protein transcription factor, is a Golgi membrane protein related to giantin |
| Q44213642 | Characterization of AtCDC48. Evidence for multiple membrane fusion mechanisms at the plane of cell division in plants |
| Q27930083 | Characterization of a novel yeast SNARE protein implicated in Golgi retrograde traffic |
| Q46444189 | Characterization of the interaction between neuronal RNA-binding protein HuD and AU-rich RNA. |
| Q36321499 | Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells. |
| Q37701779 | Components of the SNARE-containing regulon are co-regulated in root cells undergoing defense |
| Q35197965 | Control of eukaryotic membrane fusion by N-terminal domains of SNARE proteins. |
| Q37220226 | Countercurrent distribution of two distinct SNARE complexes mediating transport within the Golgi stack |
| Q27929807 | Coupled ER to Golgi transport reconstituted with purified cytosolic proteins |
| Q27639734 | Crystal structure of SEDL and its implications for a genetic disease spondyloepiphyseal dysplasia tarda |
| Q77355829 | Current views in intracellular transport: insights from studies in immunology |
| Q31011697 | Data for the effects of ER and Golgi stresses on the ER-Golgi SNARE Syntaxin5 expression and on the βAPP processing in cultured hippocampal neurons |
| Q31033407 | Data supporting ER stress response in NG108-15 cells involves upregulation of syntaxin 5 expression and reduced amyloid β peptide secretion |
| Q42648486 | Deep coverage mouse red blood cell proteome: a first comparison with the human red blood cell |
| Q31149681 | Deletion of the SNARE vti1b in mice results in the loss of a single SNARE partner, syntaxin 8. |
| Q57097441 | Dimethylformamide is not better than glycerol for cryopreservation of boar semen |
| Q24534126 | Distinct SNARE complexes mediating membrane fusion in Golgi transport based on combinatorial specificity |
| Q35799558 | Distinct roles for the AAA ATPases NSF and p97 in the secretory pathway |
| Q64939137 | Diverse Role of SNARE Protein Sec22 in Vesicle Trafficking, Membrane Fusion, and Autophagy. |
| Q38919078 | ER stress response in NG108-15 cells involves upregulation of syntaxin 5 expression and reduced amyloid β peptide secretion |
| Q51465546 | ER to Golgi-Dependent Protein Secretion: The Conventional Pathway. |
| Q89696762 | ER-to-Golgi Trafficking and Its Implication in Neurological Diseases |
| Q37863963 | Entry and exit mechanisms at the cis-face of the Golgi complex |
| Q59051650 | Functional architecture of an intracellular membrane t-SNARE |
| Q47855834 | Functional assays for the assessment of the pathogenicity of variants of GOSR2, an ER-to-Golgi SNARE involved in progressive myoclonus epilepsies. |
| Q28579141 | GS15, a 15-kilodalton Golgi soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) homologous to rbet1 |
| Q24644645 | GS32, a novel Golgi SNARE of 32 kDa, interacts preferentially with syntaxin 6 |
| Q47721683 | Getting into the Golgi |
| Q47721647 | Getting through the Golgi complex |
| Q39383957 | Golgi-SNARE GS28 potentiates cisplatin-induced apoptosis by forming GS28-MDM2-p53 complexes and by preventing the ubiquitination and degradation of p53. |
| Q24317233 | Hsec22c: a homolog of yeast Sec22p and mammalian rsec22a and msec22b/ERS-24 |
| Q28508489 | Identification of an axotomy-induced glycosylated protein, AIGP1, possibly involved in cell death triggered by endoplasmic reticulum-Golgi stress |
| Q53547571 | Immuno-electron tomography of ER exit sites reveals the existence of free COPII-coated transport carriers. |
| Q53516281 | Impact of the serum- and glucocorticoid-inducible kinase 1 on platelet dense granule biogenesis and secretion. |
| Q44092663 | In search of the molecular mechanism of intracellular membrane fusion and neurotransmitter release |
| Q47828256 | In vitro synthesis of sulfated glycosaminoglycans coupled to inter-compartmental Golgi transport. |
| Q35906628 | Intracellular trafficking and secretion of VLDL. |
| Q24298761 | Involvement of a novel Q-SNARE, D12, in quality control of the endomembrane system |
| Q35071674 | Involvement of syntaxin 18, an endoplasmic reticulum (ER)-localized SNARE protein, in ER-mediated phagocytosis. |
| Q30486269 | KEGG orthology-based annotation of the predicted proteome of Acropora digitifera: ZoophyteBase - an open access and searchable database of a coral genome. |
| Q28485632 | Legionella pneumophila regulates the small GTPase Rab1 activity by reversible phosphorylcholination |
| Q36399499 | Legionella subvert the functions of Rab1 and Sec22b to create a replicative organelle. |
| Q24682651 | Localization, dynamics, and protein interactions reveal distinct roles for ER and Golgi SNAREs |
| Q28579640 | Mammalian ykt6 is a neuronal SNARE targeted to a specialized compartment by its profilin-like amino terminal domain |
| Q37026524 | Manipulation of rab GTPase function by intracellular bacterial pathogens |
| Q28591768 | Mapping of R-SNARE function at distinct intracellular GLUT4 trafficking steps in adipocytes |
| Q74278666 | Megavesicles implicated in the rapid transport of intracisternal aggregates across the Golgi stack |
| Q29614426 | Membrane fusion and exocytosis |
| Q42362324 | Membrane tension increases fusion efficiency of model membranes in the presence of SNAREs |
| Q24309498 | Molecular cloning and localization of human syntaxin 16, a member of the syntaxin family of SNARE proteins |
| Q33825611 | Molecular pathogenesis of infections caused by Legionella pneumophila |
| Q37089621 | Monoubiquitination of Syntaxin 5 Regulates Golgi Membrane Dynamics during the Cell Cycle |
| Q38609841 | Morphological and functional association of Sec22b/ERS-24 with the pre-Golgi intermediate compartment |
| Q42377339 | Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity |
| Q24290265 | Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and betaAPP processing |
| Q33779916 | Organization of the ER-Golgi interface for membrane traffic control |
| Q37306202 | Oxysterol-binding protein (OSBP) is required for the perinuclear localization of intra-Golgi v-SNAREs |
| Q24297647 | Participation of the syntaxin 5/Ykt6/GS28/GS15 SNARE complex in transport from the early/recycling endosome to the trans-Golgi network |
| Q36381406 | Peri-Golgi vesicles contain retrograde but not anterograde proteins consistent with the cisternal progression model of intra-Golgi transport |
| Q33889294 | Phospholipid transfer proteins and physiological functions |
| Q34667916 | Putative fusogenic activity of NSF is restricted to a lipid mixture whose coalescence is also triggered by other factors |
| Q28580997 | R-SNARE ykt6 resides in membrane-associated protease-resistant protein particles and modulates cell cycle progression when over-expressed |
| Q39209369 | Rab1b overexpression modifies Golgi size and gene expression in HeLa cells and modulates the thyrotrophin response in thyroid cells in culture |
| Q49170436 | Rs2459976 in ZW10 gene associated with congenital heart diseases in Chinese Han population |
| Q41608272 | SNARE interactions are not selective. Implications for membrane fusion specificity |
| Q92483275 | SNARE protein SEC22B regulates early embryonic development |
| Q50336120 | SNARE status regulates tether recruitment and function in homotypic COPII vesicle fusion |
| Q41566661 | SNAREs and NSF in targeted membrane fusion |
| Q28280386 | SNAREs and membrane fusion in the Golgi apparatus |
| Q22254210 | SNAREs contribute to the specificity of membrane fusion |
| Q34692029 | Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthase |
| Q41829947 | Sec22 regulates endoplasmic reticulum morphology but not autophagy and is required for eye development in Drosophila. |
| Q39807719 | Sec22b is a negative regulator of phagocytosis in macrophages |
| Q37222548 | Sec24C/D-isoform-specific sorting of the preassembled ER-Golgi Q-SNARE complex. |
| Q42257801 | Selective control of SNARE recycling by Golgi retention |
| Q43560397 | Sequential involvement of p115, SNAREs, and Rab proteins in intra-Golgi protein transport |
| Q24673491 | Sequential tethering of Golgins and catalysis of SNAREpin assembly by the vesicle-tethering protein p115 |
| Q24308782 | Seven novel mammalian SNARE proteins localize to distinct membrane compartments |
| Q28141448 | Subunit structure of a mammalian ER/Golgi SNARE complex |
| Q28140261 | Syntaxin 13 is a developmentally regulated SNARE involved in neurite outgrowth and endosomal trafficking |
| Q24682732 | Syntaxin 13 mediates cycling of plasma membrane proteins via tubulovesicular recycling endosomes |
| Q24301008 | Syntaxin 16 and syntaxin 5 are required for efficient retrograde transport of several exogenous and endogenous cargo proteins |
| Q22254741 | Syntaxin 17 is abundant in steroidogenic cells and implicated in smooth endoplasmic reticulum membrane dynamics |
| Q22254009 | Syntaxin 18, a SNAP receptor that functions in the endoplasmic reticulum, intermediate compartment, and cis-Golgi vesicle trafficking |
| Q28264896 | Syntaxin 5 is a common component of the NSF- and p97-mediated reassembly pathways of Golgi cisternae from mitotic Golgi fragments in vitro |
| Q28572919 | Syntaxin 6 functions in trans-Golgi network vesicle trafficking |
| Q24678419 | Targeting of Arf-1 to the early Golgi by membrin, an ER-Golgi SNARE |
| Q34094891 | The Di-leucine motif of vesicle-associated membrane protein 4 is required for its localization and AP-1 binding |
| Q28571014 | The SNARE motif contributes to rbet1 intracellular targeting and dynamics independently of SNARE interactions |
| Q37403714 | The endoplasmic reticulum remains functionally connected by vesicular transport after its fragmentation in cells expressing Z-α1-antitrypsin |
| Q36555183 | The highly conserved COPII coat complex sorts cargo from the endoplasmic reticulum and targets it to the golgi |
| Q41200292 | The identification of the SNARE complex required for the fusion of VLDL-transport vesicle with hepatic cis-Golgi |
| Q24677983 | The mammalian protein (rbet1) homologous to yeast Bet1p is primarily associated with the pre-Golgi intermediate compartment and is involved in vesicular transport from the endoplasmic reticulum to the Golgi apparatus |
| Q39889292 | The organelle proteome of the DT40 lymphocyte cell line. |
| Q28141461 | The p115-interactive proteins GM130 and giantin participate in endoplasmic reticulum-Golgi traffic |
| Q24308766 | The presenilin 1 protein is a component of a high molecular weight intracellular complex that contains beta-catenin |
| Q41062110 | The proteolytic fragments of the Alzheimer's disease-associated presenilin-1 form heterodimers and occur as a 100-150-kDa molecular mass complex |
| Q33600192 | The specificity of vesicle trafficking: coat proteins and SNAREs |
| Q22008531 | Three novel proteins of the syntaxin/SNAP-25 family |
| Q27937369 | Two syntaxin homologues in the TGN/endosomal system of yeast |
| Q27933694 | Vam7p, a vacuolar SNAP-25 homolog, is required for SNARE complex integrity and vacuole docking and fusion |
| Q98292736 | Vesicle transport through interaction with t-SNAREs 1a (Vti1a)'s roles in neurons |
| Q24649038 | Vesicle-associated membrane protein 4 is implicated in trans-Golgi network vesicle trafficking |
| Q24305479 | Vesicle-associated membrane protein 7 is expressed in intestinal ER |
| Q45345737 | Vesicular tubular clusters between the ER and Golgi mediate concentration of soluble secretory proteins by exclusion from COPI-coated vesicles |
| Q28185724 | Ykt6 forms a SNARE complex with syntaxin 5, GS28, and Bet1 and participates in a late stage in endoplasmic reticulum-Golgi transport |
| Q24619563 | rsly1 Binding to Syntaxin 5 Is Required for Endoplasmic Reticulum-to-Golgi Transport but Does Not Promote SNARE Motif Accessibility |
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