BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 38267508)

  • 21. 20 S proteasomes are imported as precursor complexes into the nucleus of yeast.
    Lehmann A; Janek K; Braun B; Kloetzel PM; Enenkel C
    J Mol Biol; 2002 Mar; 317(3):401-13. PubMed ID: 11922673
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Distinct nuclear import and export pathways mediated by members of the karyopherin beta family.
    Moroianu J
    J Cell Biochem; 1998 Aug; 70(2):231-9. PubMed ID: 9671229
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Yeast karyopherin Kap95 is required for cell cycle progression at Start.
    Taberner FJ; Igual JC
    BMC Cell Biol; 2010 Jun; 11():47. PubMed ID: 20587033
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nuclear import of histones.
    Bernardes NE; Chook YM
    Biochem Soc Trans; 2020 Dec; 48(6):2753-2767. PubMed ID: 33300986
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Blm10 facilitates nuclear import of proteasome core particles.
    Weberruss MH; Savulescu AF; Jando J; Bissinger T; Harel A; Glickman MH; Enenkel C
    EMBO J; 2013 Oct; 32(20):2697-707. PubMed ID: 23982732
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of a yeast karyopherin heterodimer that targets import substrate to mammalian nuclear pore complexes.
    Enenkel C; Blobel G; Rexach M
    J Biol Chem; 1995 Jul; 270(28):16499-502. PubMed ID: 7622450
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Expression in yeast of binding regions of karyopherins alpha and beta inhibits nuclear import and cell growth.
    Enenkel C; Schülke N; Blobel G
    Proc Natl Acad Sci U S A; 1996 Nov; 93(23):12986-91. PubMed ID: 8917531
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Nuclear localization signal-independent and importin/karyopherin-independent nuclear import of beta-catenin.
    Fagotto F; Glück U; Gumbiner BM
    Curr Biol; 1998 Feb; 8(4):181-90. PubMed ID: 9501980
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Ubiquitin orchestrates proteasome dynamics between proliferation and quiescence in yeast.
    Gu ZC; Wu E; Sailer C; Jando J; Styles E; Eisenkolb I; Kuschel M; Bitschar K; Wang X; Huang L; Vissa A; Yip CM; Yedidi RS; Friesen H; Enenkel C
    Mol Biol Cell; 2017 Sep; 28(19):2479-2491. PubMed ID: 28768827
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Yeast importin-β is required for nuclear import of the Mig2 repressor.
    Fernández-Cid A; Vega M; Herrero P; Moreno F
    BMC Cell Biol; 2012 Nov; 13():31. PubMed ID: 23131016
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Structural basis for cell-cycle-dependent nuclear import mediated by the karyopherin Kap121p.
    Kobayashi J; Matsuura Y
    J Mol Biol; 2013 Jun; 425(11):1852-1868. PubMed ID: 23541588
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A nuclear ubiquitin-proteasome pathway targets the inner nuclear membrane protein Asi2 for degradation.
    Boban M; Pantazopoulou M; Schick A; Ljungdahl PO; Foisner R
    J Cell Sci; 2014 Aug; 127(Pt 16):3603-13. PubMed ID: 24928896
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Structural basis for nuclear import complex dissociation by RanGTP.
    Lee SJ; Matsuura Y; Liu SM; Stewart M
    Nature; 2005 Jun; 435(7042):693-6. PubMed ID: 15864302
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Karyopherin beta2 mediates nuclear import of a mRNA binding protein.
    Bonifaci N; Moroianu J; Radu A; Blobel G
    Proc Natl Acad Sci U S A; 1997 May; 94(10):5055-60. PubMed ID: 9144189
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The karyopherin Kap95 and the C-termini of Rfa1, Rfa2, and Rfa3 are necessary for efficient nuclear import of functional RPA complex proteins in Saccharomyces cerevisiae.
    Belanger KD; Griffith AL; Baker HL; Hansen JN; Kovacs LA; Seconi JS; Strine AC
    DNA Cell Biol; 2011 Sep; 30(9):641-51. PubMed ID: 21332387
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Proteasome storage granules protect proteasomes from autophagic degradation upon carbon starvation.
    Marshall RS; Vierstra RD
    Elife; 2018 Apr; 7():. PubMed ID: 29624167
    [TBL] [Abstract][Full Text] [Related]  

  • 37. AMPK regulates ESCRT-dependent microautophagy of proteasomes concomitant with proteasome storage granule assembly during glucose starvation.
    Li J; Breker M; Graham M; Schuldiner M; Hochstrasser M
    PLoS Genet; 2019 Nov; 15(11):e1008387. PubMed ID: 31738769
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The classical nuclear localization signal receptor, importin-alpha, is required for efficient transition through the G1/S stage of the cell cycle in Saccharomyces cerevisiae.
    Pulliam KF; Fasken MB; McLane LM; Pulliam JV; Corbett AH
    Genetics; 2009 Jan; 181(1):105-18. PubMed ID: 18984568
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Nuclear import of TFIIB is mediated by Kap114p, a karyopherin with multiple cargo-binding domains.
    Hodges JL; Leslie JH; Mosammaparast N; Guo Y; Shabanowitz J; Hunt DF; Pemberton LF
    Mol Biol Cell; 2005 Jul; 16(7):3200-10. PubMed ID: 15888545
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Severe acute respiratory syndrome coronavirus ORF6 antagonizes STAT1 function by sequestering nuclear import factors on the rough endoplasmic reticulum/Golgi membrane.
    Frieman M; Yount B; Heise M; Kopecky-Bromberg SA; Palese P; Baric RS
    J Virol; 2007 Sep; 81(18):9812-24. PubMed ID: 17596301
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.