scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Rita L Strack | Q42707330 |
Dibyendu Bhattacharyya | Q59217999 | ||
P2093 | author name string | Benjamin S Glick | |
Jotham R Austin | |||
Stephanie K Levi | |||
P2860 | cites work | The biogenesis of the Golgi ribbon: the roles of membrane input from the ER and of GM130. | Q24297871 |
GM130 and GRASP65-dependent lateral cisternal fusion allows uniform Golgi-enzyme distribution | Q24305177 | ||
The Golgi-associated protein GRASP65 regulates spindle dynamics and is essential for cell division | Q24531329 | ||
Mapping the interaction between GRASP65 and GM130, components of a protein complex involved in the stacking of Golgi cisternae | Q24533251 | ||
GRASP55, a second mammalian GRASP protein involved in the stacking of Golgi cisternae in a cell-free system. | Q24534390 | ||
Polo-like kinase is required for the fragmentation of pericentriolar Golgi stacks during mitosis | Q24555899 | ||
Transmembrane transforming growth factor-alpha tethers to the PDZ domain-containing, Golgi membrane-associated protein p59/GRASP55 | Q24595955 | ||
Mitotic phosphorylation of Golgi reassembly stacking protein 55 by mitogen-activated protein kinase ERK2 | Q24633683 | ||
The Tlg SNARE complex is required for TGN homotypic fusion | Q36294202 | ||
How Saccharomyces responds to nutrients | Q37096066 | ||
Characterization of the Saccharomyces Golgi complex through the cell cycle by immunoelectron microscopy | Q37373383 | ||
Golgins and GRASPs: holding the Golgi together | Q37512660 | ||
Evolution and diversity of the Golgi body | Q37616692 | ||
The yeast Golgi apparatus: insights and mysteries | Q37625133 | ||
GRASP65 and GRASP55 sequentially promote the transport of C-terminal valine-bearing cargos to and through the Golgi complex | Q39785802 | ||
dGRASP localization and function in the early exocytic pathway in Drosophila S2 cells | Q40405455 | ||
Plk1 docking to GRASP65 phosphorylated by Cdk1 suggests a mechanism for Golgi checkpoint signalling. | Q40464411 | ||
Membrane Dynamics at the Endoplasmic Reticulum–Golgi Interface | Q41523777 | ||
Control of Golgi morphology and function by Sed5 t-SNARE phosphorylation | Q41950771 | ||
dGRASP-mediated noncanonical integrin secretion is required for Drosophila epithelial remodeling | Q42524626 | ||
Molecular mechanism of mitotic Golgi disassembly and reassembly revealed by a defined reconstitution assay. | Q42618291 | ||
Development of the yeast Pichia pastoris as a model organism for a genetic and molecular analysis of peroxisome assembly | Q44182807 | ||
Concentration of GPI-anchored proteins upon ER exit in yeast | Q46215537 | ||
The Golgi-associated protein GRASP is required for unconventional protein secretion during development. | Q46828620 | ||
A versatile set of vectors for constitutive and regulated gene expression in Pichia pastoris | Q47796942 | ||
Sec16 is a determinant of transitional ER organization | Q48124825 | ||
Ultrastructural study of Golgi duplication in Trypanosoma brucei. | Q51829441 | ||
Adhesion of Golgi cisternae by proteinaceous interactions: intercisternal bridges as putative adhesive structures | Q54259312 | ||
Golgi maturation visualized in living yeast | Q59058669 | ||
De novo formation of transitional ER sites and Golgi structures in Pichia pastoris | Q78315009 | ||
GRASPing unconventional secretion | Q80784537 | ||
Two new Ypt GTPases are required for exit from the yeast trans-Golgi compartment | Q24678537 | ||
A direct role for GRASP65 as a mitotically regulated Golgi stacking factor | Q24681502 | ||
Golgi matrix proteins interact with p24 cargo receptors and aid their efficient retention in the Golgi apparatus | Q24685223 | ||
Proteome survey reveals modularity of the yeast cell machinery | Q27929510 | ||
The yeast orthologue of GRASP65 forms a complex with a coiled-coil protein that contributes to ER to Golgi traffic | Q27930772 | ||
Golgi structure correlates with transitional endoplasmic reticulum organization in Pichia pastoris and Saccharomyces cerevisiae | Q27931787 | ||
Order of events in the yeast secretory pathway | Q27932822 | ||
Unconventional secretion of Acb1 is mediated by autophagosomes. | Q27934275 | ||
Exploration of the function and organization of the yeast early secretory pathway through an epistatic miniarray profile | Q27935813 | ||
Global landscape of protein complexes in the yeast Saccharomyces cerevisiae | Q27938796 | ||
A role for actin, Cdc1p, and Myo2p in the inheritance of late Golgi elements in Saccharomyces cerevisiae | Q27940138 | ||
Localization of components involved in protein transport and processing through the yeast Golgi apparatus | Q27940278 | ||
New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites | Q28131597 | ||
New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae | Q28131599 | ||
Targeting, disruption, replacement, and allele rescue: integrative DNA transformation in yeast | Q28131609 | ||
PDZ domains: structural modules for protein complex assembly | Q28210680 | ||
The GM130 and GRASP65 Golgi proteins cycle through and define a subdomain of the intermediate compartment | Q28214965 | ||
The ER-Golgi intermediate compartment (ERGIC): in search of its identity and function | Q28242135 | ||
GRASP65, a protein involved in the stacking of Golgi cisternae | Q28252739 | ||
PCR-synthesis of marker cassettes with long flanking homology regions for gene disruptions in S. cerevisiae | Q28295796 | ||
Mapping the functional domains of the Golgi stacking factor GRASP65 | Q28296248 | ||
Localization of large ADP-ribosylation factor-guanine nucleotide exchange factors to different Golgi compartments: evidence for distinct functions in protein traffic | Q28573549 | ||
Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells | Q29547331 | ||
Target of rapamycin in yeast, TOR2, is an essential phosphatidylinositol kinase homolog required for G1 progression | Q29616821 | ||
Plasmodium falciparum possesses two GRASP proteins that are differentially targeted to the Golgi complex via a higher- and lower-eukaryote-like mechanism | Q30044097 | ||
GRASP55 regulates Golgi ribbon formation | Q30482503 | ||
Tomographic evidence for continuous turnover of Golgi cisternae in Pichia pastoris | Q30485189 | ||
Requirements for transitional endoplasmic reticulum site structure and function in Saccharomyces cerevisiae | Q30494268 | ||
Morphogenesis and dynamics of the yeast Golgi apparatus | Q31869432 | ||
GRASP55 and GRASP65 play complementary and essential roles in Golgi cisternal stacking | Q33615083 | ||
Unconventional secretion of Pichia pastoris Acb1 is dependent on GRASP protein, peroxisomal functions, and autophagosome formation. | Q33689637 | ||
Dual anchoring of the GRASP membrane tether promotes trans pairing | Q33855302 | ||
Transport between ER and Golgi | Q33954523 | ||
Mechanisms of regulated unconventional protein secretion | Q34915147 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 9 | |
P304 | page(s) | 1168-1179 | |
P577 | publication date | 2010-06-21 | |
P1433 | published in | Traffic | Q1572846 |
P1476 | title | The yeast GRASP Grh1 colocalizes with COPII and is dispensable for organizing the secretory pathway | |
P478 | volume | 11 |
Q98208984 | A minimal self-organisation model of the Golgi apparatus |
Q34359527 | A three-stage model of Golgi structure and function |
Q35798534 | Analysis of tubulin alpha-1A/1B C-terminal tail post-translational poly-glutamylation reveals novel modification sites. |
Q38017030 | Autophagy intersections with conventional and unconventional secretion in tissue development, remodeling and inflammation |
Q35621009 | Biogenesis of a novel compartment for autophagosome-mediated unconventional protein secretion |
Q50116932 | Budding Yeast Has a Minimal Endomembrane System. |
Q34506701 | COPI selectively drives maturation of the early Golgi |
Q34414972 | Contact of cis-Golgi with ER exit sites executes cargo capture and delivery from the ER |
Q38265519 | Control systems and coordination protocols of the secretory pathway |
Q39498522 | Differential selection of Golgi proteins by COPII Sec24 isoforms in procyclic Trypanosoma brucei |
Q40991389 | ER arrival sites for COPI vesicles localize to hotspots of membrane trafficking. |
Q37167928 | ER exit sites are physical and functional core autophagosome biogenesis components |
Q37863963 | Entry and exit mechanisms at the cis-face of the Golgi complex |
Q26771341 | GRASPs in Golgi Structure and Function |
Q34036999 | Golgi compartmentation and identity |
Q30560940 | Golgi enlargement in Arf-depleted yeast cells is due to altered dynamics of cisternal maturation |
Q92965370 | Golgin45-Syntaxin5 Interaction Contributes to Structural Integrity of the Golgi Stack |
Q40156649 | Integrated self-organization of transitional ER and early Golgi compartments |
Q92282189 | Maturation-driven transport and AP-1-dependent recycling of a secretory cargo in the Golgi |
Q37571210 | Membrane adhesion dictates Golgi stacking and cisternal morphology |
Q34178527 | New components of the Golgi matrix |
Q41543991 | Phosphorylation of Chs2p regulates interaction with COPII. |
Q36518193 | Plasma membrane growth during the cell cycle: unsolved mysteries and recent progress |
Q27003285 | Putative biomarkers and targets of estrogen receptor negative human breast cancer |
Q41186025 | Regulators of ribonucleotide reductase inhibit Ty1 mobility in saccharomyces cerevisiae |
Q41883607 | Remodeling of secretory compartments creates CUPS during nutrient starvation |
Q36865153 | Retrograde traffic from the Golgi to the endoplasmic reticulum |
Q27679874 | Sec16 influences transitional ER sites by regulating rather than organizing COPII. |
Q36575114 | Secreted Acb1 Contributes to the Yeast-to-Hypha Transition in Cryptococcus neoformans |
Q87910204 | Stochastic Model of Maturation and Vesicular Exchange in Cellular Organelles |
Q38001076 | The DSL1 complex: the smallest but not the least CATCHR. |
Q38631626 | The Golgin protein Coy1 functions in intra-Golgi retrograde transport and interacts with the COG complex and Golgi SNAREs |
Q38088350 | The secretory pathway: exploring yeast diversity |
Q57794729 | The yeast GRASP Grh1 displays a high polypeptide backbone mobility along with an amyloidogenic behavior |
Q34237397 | The yeast Golgi apparatus |
Q53001273 | Three-dimensional and immune electron microscopic analysis of the secretory pathway in Saccharomyces cerevisiae. |
Q37955954 | Vesicular transport systems in fungi |
Q38104257 | Where do they come from and where do they go: candidates for regulating extracellular vesicle formation in fungi |
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