Pages that link to "Q78315009"
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The following pages link to De novo formation of transitional ER sites and Golgi structures in Pichia pastoris (Q78315009):
Displaying 50 items.
- The coiled-coil membrane protein golgin-84 is a novel rab effector required for Golgi ribbon formation (Q24292939) (← links)
- Sphingomyelin synthase-related protein SMSr controls ceramide homeostasis in the ER (Q24337469) (← links)
- Assembly, organization, and function of the COPII coat (Q24655263) (← links)
- The localization and phosphorylation of p47 are important for Golgi disassembly-assembly during the cell cycle (Q24674944) (← links)
- Two mammalian Sec16 homologues have nonredundant functions in endoplasmic reticulum (ER) export and transitional ER organization (Q24685724) (← links)
- Distribution of cortical endoplasmic reticulum determines positioning of endocytic events in yeast plasma membrane (Q27304682) (← links)
- Sec16 influences transitional ER sites by regulating rather than organizing COPII. (Q27679874) (← links)
- Live imaging of yeast Golgi cisternal maturation. (Q27930311) (← links)
- Hph1p and Hph2p, novel components of calcineurin-mediated stress responses in Saccharomyces cerevisiae (Q27930998) (← links)
- Nuclear mRNA export requires specific FG nucleoporins for translocation through the nuclear pore complex (Q27931590) (← links)
- Atg9 cycles between mitochondria and the pre-autophagosomal structure in yeasts (Q27931774) (← links)
- Regulation of PI4,5P2 synthesis by nuclear-cytoplasmic shuttling of the Mss4 lipid kinase (Q27932306) (← links)
- Golgi inheritance in small buds of Saccharomyces cerevisiae is linked to endoplasmic reticulum inheritance (Q27934714) (← links)
- ER membrane-bending proteins are necessary for de novo nuclear pore formation (Q27936599) (← links)
- Myo4p and She3p are required for cortical ER inheritance in Saccharomyces cerevisiae (Q27939586) (← links)
- Plasmodium falciparum Sec24 marks transitional ER that exports a model cargo via a diacidic motif (Q27972576) (← links)
- Sec12 binds to Sec16 at transitional ER sites (Q28480558) (← links)
- Cdc2 kinase-dependent disassembly of endoplasmic reticulum (ER) exit sites inhibits ER-to-Golgi vesicular transport during mitosis (Q28589712) (← links)
- De novo formation, fusion and fission of mammalian COPII-coated endoplasmic reticulum exit sites (Q30476542) (← links)
- Cis-Golgi matrix proteins move directly to endoplasmic reticulum exit sites by association with tubules. (Q30476638) (← links)
- Golgi inheritance in mammalian cells is mediated through endoplasmic reticulum export activities (Q30476706) (← links)
- Ordered assembly of the duplicating Golgi in Trypanosoma brucei (Q30477368) (← links)
- Identification and characterization of COPIa- and COPIb-type vesicle classes associated with plant and algal Golgi. (Q30478704) (← links)
- The actomyosin ring recruits early secretory compartments to the division site in fission yeast. (Q30481392) (← links)
- Adaptation of endoplasmic reticulum exit sites to acute and chronic increases in cargo load (Q30483089) (← links)
- Tomographic evidence for continuous turnover of Golgi cisternae in Pichia pastoris (Q30485189) (← links)
- Requirements for transitional endoplasmic reticulum site structure and function in Saccharomyces cerevisiae (Q30494268) (← links)
- The yeast GRASP Grh1 colocalizes with COPII and is dispensable for organizing the secretory pathway. (Q30495976) (← links)
- Cis-Golgi cisternal assembly and biosynthetic activation occur sequentially in plants and algae. (Q30538687) (← links)
- Golgi enlargement in Arf-depleted yeast cells is due to altered dynamics of cisternal maturation (Q30560940) (← links)
- An improved reversibly dimerizing mutant of the FK506-binding protein FKBP (Q30820499) (← links)
- Cloning and disruption of the PpURA5 gene and construction of a set of integration vectors for the stable genetic modification of Pichia pastoris (Q31025873) (← links)
- Dynamics of COPII vesicles and the Golgi apparatus in cultured Nicotiana tabacum BY-2 cells provides evidence for transient association of Golgi stacks with endoplasmic reticulum exit sites. (Q33213541) (← links)
- ER-to-Golgi transport by COPII vesicles in Arabidopsis involves a ribosome-excluding scaffold that is transferred with the vesicles to the Golgi matrix. (Q33346061) (← links)
- Mechanisms of organelle biogenesis govern stochastic fluctuations in organelle abundance (Q33715200) (← links)
- Capacity of the Golgi Apparatus for Biogenesis from the Endoplasmic Reticulum (Q33763505) (← links)
- Scaling properties of cell and organelle size (Q33983759) (← links)
- Regulation of coat assembly--sorting things out at the ER. (Q34020488) (← links)
- PpATG9 encodes a novel membrane protein that traffics to vacuolar membranes, which sequester peroxisomes during pexophagy in Pichia pastoris (Q34049834) (← links)
- Normal telomere length maintenance in Saccharomyces cerevisiae requires nuclear import of the ever shorter telomeres 1 (Est1) protein via the importin alpha pathway (Q34057250) (← links)
- Unraveling the Golgi ribbon (Q34147309) (← links)
- A microbial biomanufacturing platform for natural and semisynthetic opioids (Q34207138) (← links)
- A three-stage model of Golgi structure and function (Q34359527) (← links)
- Contact of cis-Golgi with ER exit sites executes cargo capture and delivery from the ER (Q34414972) (← links)
- COPI selectively drives maturation of the early Golgi (Q34506701) (← links)
- Inheritance and biogenesis of organelles in the secretory pathway (Q34628756) (← links)
- Nanoscale architecture of endoplasmic reticulum export sites and of Golgi membranes as determined by electron tomography. (Q34804045) (← links)
- More than one way to replicate the Golgi apparatus (Q34932349) (← links)
- Capacity of the Golgi apparatus for cargo transport prior to complete assembly (Q35010311) (← links)
- Journeys through the Golgi--taking stock in a new era. (Q35015163) (← links)