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 *

132 related articles for article (PubMed ID: 27014328)

  • 1. The Evolutionarily Conserved E3 Ubiquitin Ligase AtCHIP Contributes to Plant Immunity.
    Copeland C; Ao K; Huang Y; Tong M; Li X
    Front Plant Sci; 2016; 7():309. PubMed ID: 27014328
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HSP90s are required for NLR immune receptor accumulation in Arabidopsis.
    Huang S; Monaghan J; Zhong X; Lin L; Sun T; Dong OX; Li X
    Plant J; 2014 Aug; 79(3):427-39. PubMed ID: 24889324
    [TBL] [Abstract][Full Text] [Related]  

  • 3. AtCHIP functions as an E3 ubiquitin ligase of protein phosphatase 2A subunits and alters plant response to abscisic acid treatment.
    Luo J; Shen G; Yan J; He C; Zhang H
    Plant J; 2006 May; 46(4):649-57. PubMed ID: 16640601
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The chloroplast protease subunit ClpP4 is a substrate of the E3 ligase AtCHIP and plays an important role in chloroplast function.
    Shen G; Yan J; Pasapula V; Luo J; He C; Clarke AK; Zhang H
    Plant J; 2007 Jan; 49(2):228-37. PubMed ID: 17241447
    [TBL] [Abstract][Full Text] [Related]  

  • 5. AtCDC48A is involved in the turnover of an NLR immune receptor.
    Copeland C; Woloshen V; Huang Y; Li X
    Plant J; 2016 Oct; 88(2):294-305. PubMed ID: 27340941
    [TBL] [Abstract][Full Text] [Related]  

  • 6. AtCHIP, a U-box-containing E3 ubiquitin ligase, plays a critical role in temperature stress tolerance in Arabidopsis.
    Yan J; Wang J; Li Q; Hwang JR; Patterson C; Zhang H
    Plant Physiol; 2003 Jun; 132(2):861-9. PubMed ID: 12805616
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The E3 ligase AtCHIP ubiquitylates FtsH1, a component of the chloroplast FtsH protease, and affects protein degradation in chloroplasts.
    Shen G; Adam Z; Zhang H
    Plant J; 2007 Oct; 52(2):309-21. PubMed ID: 17714429
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The E3 ligase AtCHIP positively regulates Clp proteolytic subunit homeostasis.
    Wei J; Qiu X; Chen L; Hu W; Hu R; Chen J; Sun L; Li L; Zhang H; Lv Z; Shen G
    J Exp Bot; 2015 Sep; 66(19):5809-20. PubMed ID: 26085677
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The proteasome regulator PTRE1 contributes to the turnover of SNC1 immune receptor.
    Thulasi Devendrakumar K; Copeland C; Li X
    Mol Plant Pathol; 2019 Nov; 20(11):1566-1573. PubMed ID: 31393057
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Plant TRAF Proteins Regulate NLR Immune Receptor Turnover.
    Huang S; Chen X; Zhong X; Li M; Ao K; Huang J; Li X
    Cell Host Microbe; 2016 Feb; 19(2):204-15. PubMed ID: 26867179
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Salmonella type III effector SspH2 specifically exploits the NLR co-chaperone activity of SGT1 to subvert immunity.
    Bhavsar AP; Brown NF; Stoepel J; Wiermer M; Martin DD; Hsu KJ; Imami K; Ross CJ; Hayden MR; Foster LJ; Li X; Hieter P; Finlay BB
    PLoS Pathog; 2013; 9(7):e1003518. PubMed ID: 23935490
    [TBL] [Abstract][Full Text] [Related]  

  • 12. NLR sensors meet at the SGT1-HSP90 crossroad.
    Kadota Y; Shirasu K; Guerois R
    Trends Biochem Sci; 2010 Apr; 35(4):199-207. PubMed ID: 20096590
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The HSP90-SGT1 chaperone complex for NLR immune sensors.
    Shirasu K
    Annu Rev Plant Biol; 2009; 60():139-64. PubMed ID: 19014346
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The HSP90 complex of plants.
    Kadota Y; Shirasu K
    Biochim Biophys Acta; 2012 Mar; 1823(3):689-97. PubMed ID: 22001401
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The E3 ubiquitin ligase CHIP selectively regulates mutant epidermal growth factor receptor by ubiquitination and degradation.
    Chung C; Yoo G; Kim T; Lee D; Lee CS; Cha HR; Park YH; Moon JY; Jung SS; Kim JO; Lee JC; Kim SY; Park HS; Park M; Park DI; Lim DS; Jang KW; Lee JE
    Biochem Biophys Res Commun; 2016 Oct; 479(2):152-158. PubMed ID: 27475501
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regulation of plant immune receptor accumulation through translational repression by a glycine-tyrosine-phenylalanine (GYF) domain protein.
    Wu Z; Huang S; Zhang X; Wu D; Xia S; Li X
    Elife; 2017 Mar; 6():. PubMed ID: 28362261
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Individual components of paired typical NLR immune receptors are regulated by distinct E3 ligases.
    Dong OX; Ao K; Xu F; Johnson KCM; Wu Y; Li L; Xia S; Liu Y; Huang Y; Rodriguez E; Chen X; Chen S; Zhang Y; Petersen M; Li X
    Nat Plants; 2018 Sep; 4(9):699-710. PubMed ID: 30082764
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Staying in the fold: The SGT1/chaperone machinery in maintenance and evolution of leucine-rich repeat proteins.
    Stuttmann J; Parker JE; Noël LD
    Plant Signal Behav; 2008 May; 3(5):283-5. PubMed ID: 19513219
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Stoichiometric Interaction of the Hsp90-Sgt1-Rar1 Complex by CD and SRCD Spectroscopy.
    Siligardi G; Zhang M; Prodromou C
    Front Mol Biosci; 2017; 4():95. PubMed ID: 29387685
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The putative kinase substrate MUSE7 negatively impacts the accumulation of NLR proteins.
    Johnson KC; Zhao J; Wu Z; Roth C; Lipka V; Wiermer M; Li X
    Plant J; 2017 Mar; 89(6):1174-1183. PubMed ID: 28004865
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.