Pages that link to "Q36254668"
Jump to navigation
Jump to search
The following pages link to In vivo dynamics of nuclear pore complexes in yeast (Q36254668):
Displaying 50 items.
- The nucleoporin Nup153 is required for nuclear pore basket formation, nuclear pore complex anchoring and import of a subset of nuclear proteins (Q24535824) (← links)
- Nuclear pore complexes form immobile networks and have a very low turnover in live mammalian cells (Q24654097) (← links)
- Plasma membrane localization is required for RGS4 function in Saccharomyces cerevisiae (Q24674857) (← links)
- The vacuolar DHHC-CRD protein Pfa3p is a protein acyltransferase for Vac8p (Q24678955) (← links)
- Isolation and characterization of new Saccharomyces cerevisiae mutants perturbed in nuclear pore complex assembly (Q24803010) (← links)
- A mechanism for asymmetric segregation of age during yeast budding (Q27929801) (← links)
- Saccharomyces cerevisiae MPS2 encodes a membrane protein localized at the spindle pole body and the nuclear envelope (Q27930257) (← links)
- A novel complex of membrane proteins required for formation of a spherical nucleus. (Q27930286) (← links)
- A novel allele of Saccharomyces cerevisiae NDC1 reveals a potential role for the spindle pole body component Ndc1p in nuclear pore assembly (Q27930634) (← links)
- Novel role for a Saccharomyces cerevisiae nucleoporin, Nup170p, in chromosome segregation. (Q27932004) (← links)
- A novel fluorescence-based genetic strategy identifies mutants of Saccharomyces cerevisiae defective for nuclear pore complex assembly (Q27933301) (← links)
- Nup2p dynamically associates with the distal regions of the yeast nuclear pore complex (Q27933375) (← links)
- Structure-function mapping of a heptameric module in the nuclear pore complex. (Q27933557) (← links)
- Subcellular distribution of proteasomes implicates a major location of protein degradation in the nuclear envelope-ER network in yeast (Q27934291) (← links)
- The GLFG regions of Nup116p and Nup100p serve as binding sites for both Kap95p and Mex67p at the nuclear pore complex (Q27935647) (← links)
- ER membrane-bending proteins are necessary for de novo nuclear pore formation (Q27936599) (← links)
- Nuclear Accumulation of the Small GTPase Gsp1p Depends on Nucleoporins Nup133p, Rat2p/Nup120p, Nup85p, Nic96p, and the Acetyl-CoA Carboxylase Acc1p (Q27937534) (← links)
- A structure/function analysis of Rat7p/Nup159p, an essential nucleoporin of Saccharomyces cerevisiae (Q27937837) (← links)
- The nuclear basket proteins Mlp1p and Mlp2p are part of a dynamic interactome including Esc1p and the proteasome. (Q27938485) (← links)
- The integral membrane protein Pom34p functionally links nucleoporin subcomplexes (Q27938646) (← links)
- The karyopherin Kap95 regulates nuclear pore complex assembly into intact nuclear envelopes in vivo (Q27938827) (← links)
- The bipartite nuclear localization sequence of Rpn2 is required for nuclear import of proteasomal base complexes via karyopherin alphabeta and proteasome functions (Q27939320) (← links)
- An essential nuclear envelope integral membrane protein, Brr6p, required for nuclear transport (Q27939551) (← links)
- Nuclear export of the yeast mRNA-binding protein Nab2 is linked to a direct interaction with Gfd1 and to Gle1 function (Q27940185) (← links)
- Saccharomyces cerevisiae Ndc1p is a shared component of nuclear pore complexes and spindle pole bodies (Q27940274) (← links)
- From nucleoporins to nuclear pore complexes (Q28238651) (← links)
- Nuclear membrane dynamics and reassembly in living cells: targeting of an inner nuclear membrane protein in interphase and mitosis (Q29620018) (← links)
- Nuclear fusion and genome encounter during yeast zygote formation (Q30438859) (← links)
- Immobility, inheritance and plasticity of shape of the yeast nucleus (Q30481145) (← links)
- Single molecule studies of nucleocytoplasmic transport (Q30502699) (← links)
- Motor-driven motility of fungal nuclear pores organizes chromosomes and fosters nucleocytoplasmic transport (Q30524014) (← links)
- A fluorescent reporter for mapping cellular protein-protein interactions in time and space. (Q30538538) (← links)
- The transmission of nuclear pore complexes to daughter cells requires a cytoplasmic pool of Nsp1 (Q30555736) (← links)
- Relating whole-genome expression data with protein-protein interactions (Q30669147) (← links)
- Visualization of nuclear pore complex and its distribution by confocal laser scanning microscopy. (Q30783418) (← links)
- Toward a consensus on the mechanism of nuclear pore complex inheritance. (Q33728285) (← links)
- Function and assembly of nuclear pore complex proteins (Q33765363) (← links)
- Nuclear pore complexes: dynamics in unexpected places (Q34305908) (← links)
- Nucleocytoplasmic transport in the midzone membrane domain controls yeast mitotic spindle disassembly (Q35594571) (← links)
- Nuclear pore complex integrity requires Lnp1, a regulator of cortical endoplasmic reticulum (Q36063779) (← links)
- Biological implications of cell fusion. (Q36163604) (← links)
- The Ran GTPase cycle is required for yeast nuclear pore complex assembly (Q36323156) (← links)
- Nuclear Pore Complex Number and Distribution throughout theSaccharomyces cerevisiaeCell Cycle by Three-Dimensional Reconstruction from Electron Micrographs of Nuclear Envelopes (Q36941909) (← links)
- Dual lipid modification motifs in G(alpha) and G(gamma) subunits are required for full activity of the pheromone response pathway in Saccharomyces cerevisiae (Q38480070) (← links)
- The Malleable Nature of the Budding Yeast Nuclear Envelope: Flares, Fusion, and Fenestrations. (Q38748059) (← links)
- The Dbp5 cycle at the nuclear pore complex during mRNA export I: dbp5 mutants with defects in RNA binding and ATP hydrolysis define key steps for Nup159 and Gle1 (Q39541546) (← links)
- 3D nuclear architecture reveals coupled cell cycle dynamics of chromatin and nuclear pores in the malaria parasite Plasmodium falciparum. (Q39584956) (← links)
- Nucleocytoplasmic transport: the last 200 nanometers (Q41708889) (← links)
- Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression. (Q47991641) (← links)
- RGS4 binds to membranes through an amphipathic alpha -helix. (Q52538794) (← links)