BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 16650828)

  • 1. The proteasome activator PA28 functions in collaboration with Hsp90 in vivo.
    Minami M; Shinozaki F; Suzuki M; Yoshimatsu K; Ichikawa Y; Minami Y
    Biochem Biophys Res Commun; 2006 Jun; 344(4):1315-9. PubMed ID: 16650828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The non-canonical Hop protein from Caenorhabditis elegans exerts essential functions and forms binary complexes with either Hsc70 or Hsp90.
    Gaiser AM; Brandt F; Richter K
    J Mol Biol; 2009 Aug; 391(3):621-34. PubMed ID: 19559711
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cell cycle control by daf-21/Hsp90 at the first meiotic prophase/metaphase boundary during oogenesis in Caenorhabditis elegans.
    Inoue T; Hirata K; Kuwana Y; Fujita M; Miwa J; Roy R; Yamaguchi Y
    Dev Growth Differ; 2006 Jan; 48(1):25-32. PubMed ID: 16466390
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lipophilic regulator of a developmental switch in Caenorhabditis elegans.
    Gill MS; Held JM; Fisher AL; Gibson BW; Lithgow GJ
    Aging Cell; 2004 Dec; 3(6):413-21. PubMed ID: 15569358
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Role of the myosin assembly protein UNC-45 as a molecular chaperone for myosin.
    Barral JM; Hutagalung AH; Brinker A; Hartl FU; Epstein HF
    Science; 2002 Jan; 295(5555):669-71. PubMed ID: 11809970
    [TBL] [Abstract][Full Text] [Related]  

  • 6. C. elegans STI-1, the homolog of Sti1/Hop, is involved in aging and stress response.
    Song HO; Lee W; An K; Lee HS; Cho JH; Park ZY; Ahnn J
    J Mol Biol; 2009 Jul; 390(4):604-17. PubMed ID: 19467242
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A critical role for the proteasome activator PA28 in the Hsp90-dependent protein refolding.
    Minami Y; Kawasaki H; Minami M; Tanahashi N; Tanaka K; Yahara I
    J Biol Chem; 2000 Mar; 275(12):9055-61. PubMed ID: 10722756
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Proteasomal dysfunction activates the transcription factor SKN-1 and produces a selective oxidative-stress response in Caenorhabditis elegans.
    Kahn NW; Rea SL; Moyle S; Kell A; Johnson TE
    Biochem J; 2008 Jan; 409(1):205-13. PubMed ID: 17714076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Opposing effects of an F-box protein and the HSP90 chaperone network on microtubule stability and neurite growth in
    Zheng C; Atlas E; Lee HMT; Jao SLJ; Nguyen KCQ; Hall DH; Chalfie M
    Development; 2020 Jun; 147(12):. PubMed ID: 32467239
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chaperone-interacting TPR proteins in Caenorhabditis elegans.
    Haslbeck V; Eckl JM; Kaiser CJ; Papsdorf K; Hessling M; Richter K
    J Mol Biol; 2013 Aug; 425(16):2922-39. PubMed ID: 23727266
    [TBL] [Abstract][Full Text] [Related]  

  • 11. NCR-1 and NCR-2, the C. elegans homologs of the human Niemann-Pick type C1 disease protein, function upstream of DAF-9 in the dauer formation pathways.
    Li J; Brown G; Ailion M; Lee S; Thomas JH
    Development; 2004 Nov; 131(22):5741-52. PubMed ID: 15509773
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Application of RNAi technology and fluorescent protein markers to study membrane traffic in Caenorhabditis elegans.
    Poteryaev D; Spang A
    Methods Mol Biol; 2008; 440():331-47. PubMed ID: 18369957
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reverse genetic analysis of the Caenorhabditis elegans 26S proteasome subunits by RNA interference.
    Takahashi M; Iwasaki H; Inoue H; Takahashi K
    Biol Chem; 2002; 383(7-8):1263-6. PubMed ID: 12437114
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regulation of lead toxicity by heat shock protein 90 (daf-21) is affected by temperature in Caenorhabditis elegans.
    Wang Y; Xu S; Liu J; Zhang Y; Guo TL
    Ecotoxicol Environ Saf; 2014 Jun; 104():317-22. PubMed ID: 24726945
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of ligands for DAF-12 that govern dauer formation and reproduction in C. elegans.
    Motola DL; Cummins CL; Rottiers V; Sharma KK; Li T; Li Y; Suino-Powell K; Xu HE; Auchus RJ; Antebi A; Mangelsdorf DJ
    Cell; 2006 Mar; 124(6):1209-23. PubMed ID: 16529801
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lifespan extension by suppression of autophagy genes in Caenorhabditis elegans.
    Hashimoto Y; Ookuma S; Nishida E
    Genes Cells; 2009 Jun; 14(6):717-26. PubMed ID: 19469880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Both the N- and C-terminal chaperone sites of Hsp90 participate in protein refolding.
    Minami M; Nakamura M; Emori Y; Minami Y
    Eur J Biochem; 2001 Apr; 268(8):2520-4. PubMed ID: 11298772
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Downregulation of the Hsp90 system causes defects in muscle cells of Caenorhabditis elegans.
    Gaiser AM; Kaiser CJ; Haslbeck V; Richter K
    PLoS One; 2011; 6(9):e25485. PubMed ID: 21980476
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heat shock factor functions at the convergence of the stress response and developmental pathways in Caenorhabditis elegans.
    Walker GA; Thompson FJ; Brawley A; Scanlon T; Devaney E
    FASEB J; 2003 Oct; 17(13):1960-2. PubMed ID: 12897069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methylation of the sterol nucleus by STRM-1 regulates dauer larva formation in Caenorhabditis elegans.
    Hannich JT; Entchev EV; Mende F; Boytchev H; Martin R; Zagoriy V; Theumer G; Riezman I; Riezman H; Knölker HJ; Kurzchalia TV
    Dev Cell; 2009 Jun; 16(6):833-43. PubMed ID: 19531354
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.