Compounds > urea

urea and guanosine 5'-o-(3-thiotriphosphate)

urea has been researched along with guanosine 5'-o-(3-thiotriphosphate) in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (14.29)18.2507
2000's6 (85.71)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barritt, GJ; Chataway, TK1
Baranski, TJ; Fujita, T; Hansen, JL; Iiri, T; Servant, G; Sheikh, SP1
Lim, WK; Neubig, RR1
Dingus, J; Hildebrandt, JD; Knapp, DR; McIntire, WE; Schey, KL1
Baghdoyan, HA; Bernard, R; Lydic, R1
Gonsiorek, W; Hipkin, RW; Kozlowski, JA; Lavey, BJ; Lundell, DJ; Lunn, CA; Narula, S; Piwinski, JJ1
Allen, DR; Bolt, A; Chapman, GA; Knight, RL; Meissner, JW; Owen, DA; Watson, RJ1

Other Studies

7 other study(ies) available for urea and guanosine 5'-o-(3-thiotriphosphate)

ArticleYear
Studies on the iodination of a ras protein and the detection of ras polymers.
    Molecular and cellular biochemistry, 1994, Aug-17, Volume: 137, Issue:1

    Topics: Animals; Blotting, Western; Chloramines; Cross-Linking Reagents; Electrophoresis, Gel, Two-Dimensional; Female; Guanosine 5'-O-(3-Thiotriphosphate); Iodine Radioisotopes; Isoelectric Point; Isotope Labeling; Lactoperoxidase; Methods; Microspheres; Molecular Weight; Oncogene Protein p21(ras); Oogenesis; Polymers; Recombinant Fusion Proteins; Sodium Hypochlorite; Succinimides; Tosyl Compounds; Urea; Xenopus laevis

1994
Functional reconstitution of the angiotensin II type 2 receptor and G(i) activation.
    Circulation research, 2000, Oct-27, Volume: 87, Issue:9

    Topics: 3T3 Cells; Angiotensin II; Animals; Binding Sites; Cell Membrane; COS Cells; Gene Expression; GTP-Binding Proteins; Guanosine 5'-O-(3-Thiotriphosphate); Kinetics; Ligands; Mice; Peptide Fragments; Point Mutation; Receptor, Angiotensin, Type 1; Receptor, Angiotensin, Type 2; Receptors, Angiotensin; Signal Transduction; Structure-Activity Relationship; Transfection; Urea

2000
Selective inactivation of guanine-nucleotide-binding regulatory protein (G-protein) alpha and betagamma subunits by urea.
    The Biochemical journal, 2001, Mar-01, Volume: 354, Issue:Pt 2

    Topics: Animals; Blotting, Western; Catalysis; CHO Cells; Cricetinae; Dimerization; Dose-Response Relationship, Drug; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Guanosine 5'-O-(3-Thiotriphosphate); Heterotrimeric GTP-Binding Proteins; Humans; Protein Subunits; Structure-Activity Relationship; Tumor Cells, Cultured; Urea

2001
Characterization of deamidated G protein subunits.
    Methods in enzymology, 2002, Volume: 344

    Topics: Amides; Amino Acid Sequence; Dimerization; Electrophoresis, Polyacrylamide Gel; Epitopes; Guanosine 5'-O-(3-Thiotriphosphate); Guanosine Diphosphate; Heterotrimeric GTP-Binding Proteins; Indicators and Reagents; Molecular Sequence Data; Peptide Fragments; Protein Isoforms; Protein Subunits; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Urea

2002
Hypocretin-1 causes G protein activation and increases ACh release in rat pons.
    The European journal of neuroscience, 2003, Volume: 18, Issue:7

    Topics: Acetylcholine; Animals; Autoradiography; Benzoxazoles; Carrier Proteins; Dialysis; Dose-Response Relationship, Drug; Drug Interactions; GTP-Binding Proteins; Guanosine 5'-O-(3-Thiotriphosphate); In Vitro Techniques; Intracellular Signaling Peptides and Proteins; Male; Naphthyridines; Neuropeptides; Orexin Receptors; Orexins; Pons; Protein Binding; Rats; Rats, Sprague-Dawley; Receptors, G-Protein-Coupled; Receptors, Neuropeptide; Sulfur Isotopes; Time Factors; Urea

2003
Triaryl bis-sulfones as a new class of cannabinoid CB2 receptor inhibitors: identification of a lead and initial SAR studies.
    Bioorganic & medicinal chemistry letters, 2005, Feb-01, Volume: 15, Issue:3

    Topics: Amides; Cannabinoids; Cell Membrane; Guanosine 5'-O-(3-Thiotriphosphate); Humans; Ligands; Receptor, Cannabinoid, CB2; Structure-Activity Relationship; Sulfonamides; Sulfones; Urea

2005
Identification and structure-activity relationships of 1-aryl-3-piperidin-4-yl-urea derivatives as CXCR3 receptor antagonists.
    Bioorganic & medicinal chemistry letters, 2007, Feb-01, Volume: 17, Issue:3

    Topics: Animals; Chemical Phenomena; Chemistry, Physical; Chemotaxis; CHO Cells; Cricetinae; Cricetulus; Guanosine 5'-O-(3-Thiotriphosphate); In Vitro Techniques; Kinetics; Mice; Microsomes, Liver; Piperidines; Receptors, Chemokine; Receptors, CXCR3; Structure-Activity Relationship; Transfection; Urea

2007