BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 2059668)

  • 21. Divalent cations can induce the exposure of GroEL hydrophobic surfaces and strengthen GroEL hydrophobic binding interactions. Novel effects of Zn2+ GroEL interactions.
    Brazil BT; Ybarra J; Horowitz PM
    J Biol Chem; 1998 Feb; 273(6):3257-63. PubMed ID: 9452440
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Role of divalent metals in the activation and regulation of insulin receptor tyrosine kinase.
    Vicario PP; Saperstein R; Bennun A
    Biosystems; 1988; 22(1):55-66. PubMed ID: 2847822
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Lipid dependence of surface conformations of protein kinase C.
    Lester DS; Doll L; Brumfeld V; Miller IR
    Biochim Biophys Acta; 1990 May; 1039(1):33-41. PubMed ID: 2354199
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A monoclonal antibody against brain calmodulin-dependent protein kinase type II detects putative conformational changes induced by Ca2+-calmodulin.
    LeVine H; Su JL; Sahyoun NE
    Biochemistry; 1988 Aug; 27(17):6612-7. PubMed ID: 2464370
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Divalent cation and ionic strength effects on Vinca alkaloid-induced tubulin self-association.
    Lobert S; Boyd CA; Correia JJ
    Biophys J; 1997 Jan; 72(1):416-27. PubMed ID: 8994628
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Circular dichroism analysis of ligand-induced conformational changes in protein kinase C. Mechanism of translocation of the enzyme from the cytosol to the membranes and its implications.
    Boscá L; Morán F
    Biochem J; 1993 Mar; 290 ( Pt 3)(Pt 3):827-32. PubMed ID: 8457212
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The role of divalent cations in structure and function of murine adenosine deaminase.
    Cooper BF; Sideraki V; Wilson DK; Dominguez DY; Clark SW; Quiocho FA; Rudolph FB
    Protein Sci; 1997 May; 6(5):1031-7. PubMed ID: 9144774
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hepatic vasopressin receptor: differential effects of divalent cations, guanine nucleotides, and N-ethylmaleimide on agonist and antagonist interactions with the V1 subtype receptor.
    Gopalakrishnan V; McNeill JR; Sulakhe PV; Triggle CR
    Endocrinology; 1988 Aug; 123(2):922-31. PubMed ID: 2969327
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Remarkable affinity and selectivity for Cs+ and uranyl (UO22+) binding to the manganese site of the apo-water oxidation complex of photosystem II.
    Ananyev GM; Murphy A; Abe Y; Dismukes GC
    Biochemistry; 1999 Jun; 38(22):7200-9. PubMed ID: 10353831
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Studies of the cation binding properties of an oligomeric derivative of prostaglandin B1.
    Kometani T; Devlin TM; Ohnishi ST
    Prostaglandins Leukot Essent Fatty Acids; 1989 Jul; 37(1):37-43. PubMed ID: 2762366
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Circular dichroism and fluorescence studies on interaction of calmodulin (CaM) with purified (Ca2(+)-Mg2+)ATPase of erythrocyte ghosts.
    Wrzosek A; Famulski KS; Pikuła S
    Acta Biochim Pol; 1990; 37(1):173-6. PubMed ID: 2150904
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ca2+-dependent structural changes in bovine blood coagulation factor Va and its subunits.
    Laue TM; Lu R; Krieg UC; Esmon CT; Johnson AE
    Biochemistry; 1989 May; 28(11):4762-71. PubMed ID: 2765509
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Activation of three types of membrane currents by various divalent cations in identified molluscan pacemaker neurons.
    Müller TH; Swandulla D; Lux HD
    J Gen Physiol; 1989 Dec; 94(6):997-1014. PubMed ID: 2559142
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The effect of divalent cations on the conformation and function of human plasminogen.
    Stack S; Gonzalez-Gronow M; Pizzo SV
    Arch Biochem Biophys; 1991 Jan; 284(1):58-62. PubMed ID: 1899177
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Interaction of Penicillium notatum phospholipase B with divalent cations.
    Takeuchi Y
    Biochim Biophys Acta; 1988 May; 960(2):157-63. PubMed ID: 3365441
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Bidirectional modulation of GABA-gated chloride channels by divalent cations: inhibition by Ca2+ and enhancement by Mg2+.
    Schwartz RD; Wagner JP; Yu X; Martin D
    J Neurochem; 1994 Mar; 62(3):916-22. PubMed ID: 8113813
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Ligand binding results in divalent cation displacement from the alpha 2 beta 1 integrin I domain: evidence from terbium luminescence spectroscopy.
    Dickeson SK; Bhattacharyya-Pakrasi M; Mathis NL; Schlesinger PH; Santoro SA
    Biochemistry; 1998 Aug; 37(32):11280-8. PubMed ID: 9698375
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Extracellular divalent cations block a cation non-selective conductance unrelated to calcium channels in rat cardiac muscle.
    Mubagwa K; Stengl M; Flameng W
    J Physiol; 1997 Jul; 502 ( Pt 2)(Pt 2):235-47. PubMed ID: 9263906
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Divalent cation sensitivity of BK channel activation supports the existence of three distinct binding sites.
    Zeng XH; Xia XM; Lingle CJ
    J Gen Physiol; 2005 Mar; 125(3):273-86. PubMed ID: 15738049
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The structural events associated with the binding of divalent cations to beta-bungarotoxin.
    Chu YP; Cheng YC; Yang CC; Chang LS
    Toxicon; 2005 Feb; 45(2):139-45. PubMed ID: 15626362
    [TBL] [Abstract][Full Text] [Related]  

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