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PUBMED FOR HANDHELDS

Journal Abstract Search


113 related items for PubMed ID: 6743289

  • 21. Plant ureases: roles and regulation.
    Sirko A, Brodzik R.
    Acta Biochim Pol; 2000; 47(4):1189-95. PubMed ID: 11996109
    [Abstract] [Full Text] [Related]

  • 22. Model Complexes for the Nip Site of Acetyl Coenzyme A Synthase/Carbon Monoxide (CO) Dehydrogenase: Structure, Electrochemistry, and CO Reactivity.
    Bhandari A, Chandra Maji R, Mishra S, Kumar A, Barman SK, Das PP, Ghiassi KB, Olmstead MM, Patra AK.
    Inorg Chem; 2018 Nov 05; 57(21):13713-13727. PubMed ID: 30339375
    [Abstract] [Full Text] [Related]

  • 23. The nickel site of Bacillus pasteurii UreE, a urease metallo-chaperone, as revealed by metal-binding studies and X-ray absorption spectroscopy.
    Stola M, Musiani F, Mangani S, Turano P, Safarov N, Zambelli B, Ciurli S.
    Biochemistry; 2006 May 23; 45(20):6495-509. PubMed ID: 16700560
    [Abstract] [Full Text] [Related]

  • 24. Synthesis, crystal structures, DFT studies, molecular docking and urease inhibition studies of three Ni(II) complexes with a sexidentate N2O4-donor bis-Schiff base ligand.
    Wang H, Lan T, Zhang X, Zhang D, Bi C, Fan Y.
    J Inorg Biochem; 2016 Dec 23; 165():18-24. PubMed ID: 27755976
    [Abstract] [Full Text] [Related]

  • 25. A simple novel method for studying the combined inhibitory effects of ethylurea and N,N-dimethylurea on jack bean urease.
    Saboury AA, Moosavi-Movahedi AA.
    J Enzyme Inhib; 1997 Jan 23; 11(3):217-22. PubMed ID: 9204390
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  • 28. Synthesis, characterization and urease inhibition, in vitro anticancer and antileishmanial studies of Ni(II) complexes with N,N,N'-trisubstituted thioureas.
    Rauf MK, Yaseen S, Badshah A, Zaib S, Arshad R, Imtiaz-Ud-Din, Tahir MN, Iqbal J.
    J Biol Inorg Chem; 2015 Apr 23; 20(3):541-54. PubMed ID: 25604966
    [Abstract] [Full Text] [Related]

  • 29. Cloning and sequencing of a jack bean urease-encoding cDNA.
    Riddles PW, Whan V, Blakeley RL, Zerner B.
    Gene; 1992 Nov 16; 121(2):399-400. PubMed ID: 1446838
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  • 31. Inactivation of urease by catechol: Kinetics and structure.
    Mazzei L, Cianci M, Musiani F, Lente G, Palombo M, Ciurli S.
    J Inorg Biochem; 2017 Jan 16; 166():182-189. PubMed ID: 27888701
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  • 33. Synthesis, structures and urease inhibition studies of Schiff base metal complexes derived from 3,5-dibromosalicylaldehyde.
    Cui Y, Dong X, Li Y, Li Z, Chen W.
    Eur J Med Chem; 2012 Dec 16; 58():323-31. PubMed ID: 23142672
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  • 34. Redox chemistry of nickel(II) complexes supported by a series of noninnocent β-diketiminate ligands.
    Takaichi J, Morimoto Y, Ohkubo K, Shimokawa C, Hojo T, Mori S, Asahara H, Sugimoto H, Fujieda N, Nishiwaki N, Fukuzumi S, Itoh S.
    Inorg Chem; 2014 Jun 16; 53(12):6159-69. PubMed ID: 24884152
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  • 35. Increased electrophoretic mobility of sodium sulfite-treated jack bean urease.
    Martín de Llano JJ, Gavilanes JG.
    Electrophoresis; 1992 May 16; 13(5):300-4. PubMed ID: 1396524
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  • 36. Molecular docking of Glycine max and Medicago truncatula ureases with urea; bioinformatics approaches.
    Filiz E, Vatansever R, Ozyigit II.
    Mol Biol Rep; 2016 Mar 16; 43(3):129-40. PubMed ID: 26852122
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  • 37. Letter: Jack bean urease (EC 3.5.1.5). A metalloenzyme. A simple biological role for nickel?
    Dixon NE, Gazzola TC, blakeley RL, Zermer B.
    J Am Chem Soc; 1975 Jul 09; 97(14):4131-3. PubMed ID: 1159216
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  • 38. Color tuning of a nickel complex with a novel N2S2 pyridine-containing macrocyclic ligand.
    Tamayo A, Casabó J, Escriche L, Lodeiro C, Covelo B, Brondino CD, Kivekäs R, Sillampää R.
    Inorg Chem; 2006 Feb 06; 45(3):1140-9. PubMed ID: 16441124
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  • 39. Photo-oxidation of Jack bean urease in the presence of methylene blue.
    Sakaguchi K, Mitsui K, Kobashi K, Hase J.
    J Biochem; 1983 Mar 06; 93(3):681-6. PubMed ID: 6874659
    [Abstract] [Full Text] [Related]

  • 40. Realization of unusual ligand binding motifs in metalated container molecules: synthesis, structures, and magnetic properties of the complexes [(LMe)Ni2(mu-L')]n+ with L'=NO3-, NO2-, N3-, N2H4, pyridazine, phthalazine, pyrazolate, and benzoate.
    Hausmann J, Klingele MH, Lozan V, Steinfeld G, Siebert D, Journaux Y, Girerd JJ, Kersting B.
    Chemistry; 2004 Apr 02; 10(7):1716-28. PubMed ID: 15054759
    [Abstract] [Full Text] [Related]


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