BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 12917401)

  • 1. A gradient of affinity for the karyopherin Kap95p along the yeast nuclear pore complex.
    Pyhtila B; Rexach M
    J Biol Chem; 2003 Oct; 278(43):42699-709. PubMed ID: 12917401
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Accelerating the rate of disassembly of karyopherin.cargo complexes.
    Gilchrist D; Mykytka B; Rexach M
    J Biol Chem; 2002 May; 277(20):18161-72. PubMed ID: 11867631
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Structural basis for the high-affinity binding of nucleoporin Nup1p to the Saccharomyces cerevisiae importin-beta homologue, Kap95p.
    Liu SM; Stewart M
    J Mol Biol; 2005 Jun; 349(3):515-25. PubMed ID: 15878174
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The nucleoporin Nup60p functions as a Gsp1p-GTP-sensitive tether for Nup2p at the nuclear pore complex.
    Denning D; Mykytka B; Allen NP; Huang L; Al Burlingame ; Rexach M
    J Cell Biol; 2001 Sep; 154(5):937-50. PubMed ID: 11535617
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The GLFG regions of Nup116p and Nup100p serve as binding sites for both Kap95p and Mex67p at the nuclear pore complex.
    Strawn LA; Shen T; Wente SR
    J Biol Chem; 2001 Mar; 276(9):6445-52. PubMed ID: 11104765
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deciphering networks of protein interactions at the nuclear pore complex.
    Allen NP; Patel SS; Huang L; Chalkley RJ; Burlingame A; Lutzmann M; Hurt EC; Rexach M
    Mol Cell Proteomics; 2002 Dec; 1(12):930-46. PubMed ID: 12543930
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A nuclear export signal in Kap95p is required for both recycling the import factor and interaction with the nucleoporin GLFG repeat regions of Nup116p and Nup100p.
    Iovine MK; Wente SR
    J Cell Biol; 1997 May; 137(4):797-811. PubMed ID: 9151683
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The FG-repeat asymmetry of the nuclear pore complex is dispensable for bulk nucleocytoplasmic transport in vivo.
    Zeitler B; Weis K
    J Cell Biol; 2004 Nov; 167(4):583-90. PubMed ID: 15557115
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nuclear mRNA export requires specific FG nucleoporins for translocation through the nuclear pore complex.
    Terry LJ; Wente SR
    J Cell Biol; 2007 Sep; 178(7):1121-32. PubMed ID: 17875746
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Karyopherins in nuclear pore biogenesis: a role for Kap121p in the assembly of Nup53p into nuclear pore complexes.
    Lusk CP; Makhnevych T; Marelli M; Aitchison JD; Wozniak RW
    J Cell Biol; 2002 Oct; 159(2):267-78. PubMed ID: 12403813
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nup2p, a yeast nucleoporin, functions in bidirectional transport of importin alpha.
    Solsbacher J; Maurer P; Vogel F; Schlenstedt G
    Mol Cell Biol; 2000 Nov; 20(22):8468-79. PubMed ID: 11046143
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Crystal structure of the Xpo1p nuclear export complex bound to the SxFG/PxFG repeats of the nucleoporin Nup42p.
    Koyama M; Hirano H; Shirai N; Matsuura Y
    Genes Cells; 2017 Oct; 22(10):861-875. PubMed ID: 28791779
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Karyopherins regulate nuclear pore complex barrier and transport function.
    Kapinos LE; Huang B; Rencurel C; Lim RYH
    J Cell Biol; 2017 Nov; 216(11):3609-3624. PubMed ID: 28864541
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structures of the Karyopherins Kap121p and Kap60p Bound to the Nuclear Pore-Targeting Domain of the SUMO Protease Ulp1p.
    Hirano H; Kobayashi J; Matsuura Y
    J Mol Biol; 2017 Jan; 429(2):249-260. PubMed ID: 27939291
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Proteomic analysis of nucleoporin interacting proteins.
    Allen NP; Huang L; Burlingame A; Rexach M
    J Biol Chem; 2001 Aug; 276(31):29268-74. PubMed ID: 11387327
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Karyopherin-centric control of nuclear pores based on molecular occupancy and kinetic analysis of multivalent binding with FG nucleoporins.
    Kapinos LE; Schoch RL; Wagner RS; Schleicher KD; Lim RY
    Biophys J; 2014 Apr; 106(8):1751-62. PubMed ID: 24739174
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Minimal nuclear pore complexes define FG repeat domains essential for transport.
    Strawn LA; Shen T; Shulga N; Goldfarb DS; Wente SR
    Nat Cell Biol; 2004 Mar; 6(3):197-206. PubMed ID: 15039779
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A designer FG-Nup that reconstitutes the selective transport barrier of the nuclear pore complex.
    Fragasso A; de Vries HW; Andersson J; van der Sluis EO; van der Giessen E; Dahlin A; Onck PR; Dekker C
    Nat Commun; 2021 Mar; 12(1):2010. PubMed ID: 33790297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Emergence of selectivity and specificity in a coarse-grained model of the nuclear pore complex with sequence-agnostic FG-Nups.
    Patel MK; Chakrabarti B; Panwar AS
    Phys Chem Chem Phys; 2023 Dec; 25(48):32824-32836. PubMed ID: 38018404
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Natively Unfolded FG Repeats Stabilize the Structure of the Nuclear Pore Complex.
    Onischenko E; Tang JH; Andersen KR; Knockenhauer KE; Vallotton P; Derrer CP; Kralt A; Mugler CF; Chan LY; Schwartz TU; Weis K
    Cell; 2017 Nov; 171(4):904-917.e19. PubMed ID: 29033133
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.