These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 22946053)

  • 21. Misfolding and aggregation of nascent proteins: a novel mode of toxic cadmium action in vivo.
    Tamás MJ; Fauvet B; Christen P; Goloubinoff P
    Curr Genet; 2018 Feb; 64(1):177-181. PubMed ID: 28936749
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Arsenite-induced lipid peroxidation in Saccharomyces cerevisiae].
    Samokhvalov VA; Museĭkina NIu; Mel'nikov GV; Ignatov VV
    Mikrobiologiia; 2003; 72(3):308-11. PubMed ID: 12901003
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cadmium Causes Misfolding and Aggregation of Cytosolic Proteins in Yeast.
    Jacobson T; Priya S; Sharma SK; Andersson S; Jakobsson S; Tanghe R; Ashouri A; Rauch S; Goloubinoff P; Christen P; Tamás MJ
    Mol Cell Biol; 2017 Sep; 37(17):. PubMed ID: 28606932
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Role of molecular chaperones in biogenesis of the protein kinome.
    Mandal AK; Theodoraki MA; Nillegoda NB; Caplan AJ
    Methods Mol Biol; 2011; 787():75-81. PubMed ID: 21898228
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Thermal adaptation of the yeast mitochondrial Hsp70 system is regulated by the reversible unfolding of its nucleotide exchange factor.
    Moro F; Muga A
    J Mol Biol; 2006 May; 358(5):1367-77. PubMed ID: 16600294
    [TBL] [Abstract][Full Text] [Related]  

  • 26. N-Ethylmaleimide-modified Hsp70 inhibits protein folding.
    Hermawan A; Chirico WJ
    Arch Biochem Biophys; 1999 Sep; 369(1):157-62. PubMed ID: 10462452
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Inclusion body anatomy and functioning of chaperone-mediated in vivo inclusion body disassembly during high-level recombinant protein production in Escherichia coli.
    Rinas U; Hoffmann F; Betiku E; Estapé D; Marten S
    J Biotechnol; 2007 Jan; 127(2):244-57. PubMed ID: 16945443
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Protein folding sculpting evolutionary change.
    Lindquist S
    Cold Spring Harb Symp Quant Biol; 2009; 74():103-8. PubMed ID: 20375316
    [TBL] [Abstract][Full Text] [Related]  

  • 29. ZFAND1 Recruits p97 and the 26S Proteasome to Promote the Clearance of Arsenite-Induced Stress Granules.
    Turakhiya A; Meyer SR; Marincola G; Böhm S; Vanselow JT; Schlosser A; Hofmann K; Buchberger A
    Mol Cell; 2018 Jun; 70(5):906-919.e7. PubMed ID: 29804830
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A stress regulatory network for co-ordinated activation of proteasome expression mediated by yeast heat shock transcription factor.
    Hahn JS; Neef DW; Thiele DJ
    Mol Microbiol; 2006 Apr; 60(1):240-51. PubMed ID: 16556235
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Misfolding-prone proteins are reversibly sequestered to an Hsp42-associated granule upon chronological aging.
    Lee HY; Chao JC; Cheng KY; Leu JY
    J Cell Sci; 2018 Aug; 131(16):. PubMed ID: 30054385
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Trehalose is a versatile and long-lived chaperone for desiccation tolerance.
    Tapia H; Koshland DE
    Curr Biol; 2014 Dec; 24(23):2758-66. PubMed ID: 25456447
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hsp31 Is a Stress Response Chaperone That Intervenes in the Protein Misfolding Process.
    Tsai CJ; Aslam K; Drendel HM; Asiago JM; Goode KM; Paul LN; Rochet JC; Hazbun TR
    J Biol Chem; 2015 Oct; 290(41):24816-34. PubMed ID: 26306045
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Formation of Transient Protein Aggregate-like Centers Is a General Strategy Postponing Degradation of Misfolded Intermediates.
    Boronat S; Cabrera M; Vega M; Alcalá J; Salas-Pino S; Daga RR; Ayté J; Hidalgo E
    Int J Mol Sci; 2023 Jul; 24(13):. PubMed ID: 37446379
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Reversible, Specific, Active Aggregates of Endogenous Proteins Assemble upon Heat Stress.
    Wallace EW; Kear-Scott JL; Pilipenko EV; Schwartz MH; Laskowski PR; Rojek AE; Katanski CD; Riback JA; Dion MF; Franks AM; Airoldi EM; Pan T; Budnik BA; Drummond DA
    Cell; 2015 Sep; 162(6):1286-98. PubMed ID: 26359986
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Discrete roles of trehalose and Hsp104 in inhibition of protein aggregation in yeast cells.
    Sethi R; Iyer SS; Das E; Roy I
    FEMS Yeast Res; 2018 Sep; 18(6):. PubMed ID: 29860440
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Proteasome storage granules are transiently associated with the insoluble protein deposit in Saccharomyces cerevisiae.
    Peters LZ; Karmon O; Miodownik S; Ben-Aroya S
    J Cell Sci; 2016 Mar; 129(6):1190-7. PubMed ID: 26826189
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Toxicity of the model protein 3×GFP arises from degradation overload, not from aggregate formation.
    Namba S; Moriya H
    J Cell Sci; 2024 Jun; 137(11):. PubMed ID: 38766715
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A prion-like domain in Hsp42 drives chaperone-facilitated aggregation of misfolded proteins.
    Grousl T; Ungelenk S; Miller S; Ho CT; Khokhrina M; Mayer MP; Bukau B; Mogk A
    J Cell Biol; 2018 Apr; 217(4):1269-1285. PubMed ID: 29362223
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Spatially organized aggregation of misfolded proteins as cellular stress defense strategy.
    Miller SB; Mogk A; Bukau B
    J Mol Biol; 2015 Apr; 427(7):1564-74. PubMed ID: 25681695
    [TBL] [Abstract][Full Text] [Related]  

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