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 *

108 related articles for article (PubMed ID: 7768904)

  • 61. Mitogen-activated protein kinase acts as a negative regulator of the heat shock response in NIH3T3 cells.
    Mivechi NF; Giaccia AJ
    Cancer Res; 1995 Dec; 55(23):5512-9. PubMed ID: 7585624
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Stimulation of multiple mitogen-activated protein kinase sub-families by oxidative stress and phosphorylation of the small heat shock protein, HSP25/27, in neonatal ventricular myocytes.
    Clerk A; Michael A; Sugden PH
    Biochem J; 1998 Aug; 333 ( Pt 3)(Pt 3):581-9. PubMed ID: 9677316
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Proteomics studies of the interactome of RNA polymerase II C-terminal repeated domain.
    Pineda G; Shen Z; de Albuquerque CP; Reynoso E; Chen J; Tu CC; Tang W; Briggs S; Zhou H; Wang JY
    BMC Res Notes; 2015 Oct; 8():616. PubMed ID: 26515650
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Specificity determinants of substrate recognition by the protein kinase DYRK1A.
    Himpel S; Tegge W; Frank R; Leder S; Joost HG; Becker W
    J Biol Chem; 2000 Jan; 275(4):2431-8. PubMed ID: 10644696
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Constitutive activation of mitogen-activated protein kinase-activated protein kinase 2 by mutation of phosphorylation sites and an A-helix motif.
    Engel K; Schultz H; Martin F; Kotlyarov A; Plath K; Hahn M; Heinemann U; Gaestel M
    J Biol Chem; 1995 Nov; 270(45):27213-21. PubMed ID: 7592979
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Definition of a consensus sequence for peptide substrate recognition by p44mpk, the meiosis-activated myelin basic protein kinase.
    Clark-Lewis I; Sanghera JS; Pelech SL
    J Biol Chem; 1991 Aug; 266(23):15180-4. PubMed ID: 1907971
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Heat shock induces two distinct S6 protein kinase activities in quiescent mammalian fibroblasts.
    Jurivich DA; Chung J; Blenis J
    J Cell Physiol; 1991 Aug; 148(2):252-9. PubMed ID: 1880153
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Identification of c-Jun NH2-terminal protein kinase (JNK)-activating kinase 2 as an activator of JNK but not p38.
    Lu X; Nemoto S; Lin A
    J Biol Chem; 1997 Oct; 272(40):24751-4. PubMed ID: 9312068
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Cdc15 Phosphorylates the C-terminal Domain of RNA Polymerase II for Transcription during Mitosis.
    Singh AK; Rastogi S; Shukla H; Asalam M; Rath SK; Akhtar MS
    J Biol Chem; 2017 Mar; 292(13):5507-5518. PubMed ID: 28202544
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Stathmin is a major substrate for mitogen-activated protein kinase during heat shock and chemical stress in HeLa cells.
    Beretta L; Dubois MF; Sobel A; Bensaude O
    Eur J Biochem; 1995 Jan; 227(1-2):388-95. PubMed ID: 7851413
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Evidence for a role of p38 kinase in hypoxia-inducible factor 1-independent induction of vascular endothelial growth factor expression by sodium arsenite.
    Duyndam MC; Hulscher ST; van der Wall E; Pinedo HM; Boven E
    J Biol Chem; 2003 Feb; 278(9):6885-95. PubMed ID: 12482858
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Viral transactivators specifically target distinct cellular protein kinases that phosphorylate the RNA polymerase II C-terminal domain.
    Herrmann CH; Gold MO; Rice AP
    Nucleic Acids Res; 1996 Feb; 24(3):501-8. PubMed ID: 8602364
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Mitogen-activated protein kinases activate the serine/threonine kinases Mnk1 and Mnk2.
    Waskiewicz AJ; Flynn A; Proud CG; Cooper JA
    EMBO J; 1997 Apr; 16(8):1909-20. PubMed ID: 9155017
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A protein kinase from wheat germ that phosphorylates the largest subunit of RNA polymerase II.
    Guilfoyle TJ
    Plant Cell; 1989 Aug; 1(8):827-36. PubMed ID: 2535525
    [TBL] [Abstract][Full Text] [Related]  

  • 75. A common structural scaffold in CTD phosphatases that supports distinct catalytic mechanisms.
    Pons T; Paramonov I; Boullosa C; Ibáñez K; Rojas AM; Valencia A
    Proteins; 2014 Jan; 82(1):103-18. PubMed ID: 23900790
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Extracellular signal-regulated kinases in T cells. Anti-CD3 and 4 beta-phorbol 12-myristate 13-acetate-induced phosphorylation and activation.
    Whitehurst CE; Boulton TG; Cobb MH; Geppert TD
    J Immunol; 1992 May; 148(10):3230-7. PubMed ID: 1533654
    [TBL] [Abstract][Full Text] [Related]  

  • 77. The mitogen-activated protein kinase phosphatase-3 N-terminal noncatalytic region is responsible for tight substrate binding and enzymatic specificity.
    Muda M; Theodosiou A; Gillieron C; Smith A; Chabert C; Camps M; Boschert U; Rodrigues N; Davies K; Ashworth A; Arkinstall S
    J Biol Chem; 1998 Apr; 273(15):9323-9. PubMed ID: 9535927
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Insulin-activated protein kinases phosphorylate a pseudosubstrate synthetic peptide inhibitor of the p70 S6 kinase.
    Price DJ; Mukhopadhyay NK; Avruch J
    J Biol Chem; 1991 Sep; 266(25):16281-4. PubMed ID: 1909327
    [TBL] [Abstract][Full Text] [Related]  

  • 79. A novel method to identify protein kinase substrates: eEF2 kinase is phosphorylated and inhibited by SAPK4/p38delta.
    Knebel A; Morrice N; Cohen P
    EMBO J; 2001 Aug; 20(16):4360-9. PubMed ID: 11500363
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Multisite phosphorylation of a synthetic peptide derived from the carboxyl terminus of the ribosomal protein S6.
    Brandon SD; Masaracchia RA
    J Biol Chem; 1991 Jan; 266(1):380-5. PubMed ID: 1985906
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.