Page last updated: 2024-08-18

pyrazolanthrone and valine

pyrazolanthrone has been researched along with valine in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ellis, S; Fricker, M; Hunt, P; Lograsso, P; Pollack, SJ; Wilkie, N	1
Das, HK; Mueller, B; Tchedre, K	1

Other Studies

2 other study(ies) available for pyrazolanthrone and valine

Article	Year
Substituting c-Jun N-terminal kinase-3 (JNK3) ATP-binding site amino acid residues with their p38 counterparts affects binding of JNK- and p38-selective inhibitors. Archives of biochemistry and biophysics, 2005, Jun-15, Volume: 438, Issue:2 Topics: Adenosine Triphosphate; Alanine; Amino Acids; Animals; Anthracenes; Binding Sites; Biotinylation; Crystallography, X-Ray; Enzyme Inhibitors; Fluorescence Resonance Energy Transfer; Glutathione; Humans; Imidazoles; Inhibitory Concentration 50; Isoleucine; Kinetics; MAP Kinase Signaling System; Mitogen-Activated Protein Kinase 10; Models, Biological; Models, Chemical; Models, Molecular; Mutation; p38 Mitogen-Activated Protein Kinases; Phosphorylation; Point Mutation; Protein Binding; Protein Folding; Pyrimidines; Valine	2005
Repression of transcription of presenilin-1 inhibits γ-secretase independent ER Ca²⁺ leak that is impaired by FAD mutations. Journal of neurochemistry, 2012, Volume: 122, Issue:3 Topics: Amyloid Precursor Protein Secretases; Anthracenes; Calcium; Carrier Proteins; Cell Line, Tumor; Cytosol; DNA Helicases; Dose-Response Relationship, Drug; Endoplasmic Reticulum; Enzyme Inhibitors; Gene Expression Regulation, Neoplastic; Humans; Inositol 1,4,5-Trisphosphate Receptors; Methionine; Mi-2 Nucleosome Remodeling and Deacetylase Complex; Mutation; Neuroblastoma; Nuclear Proteins; Peptide Fragments; Presenilin-1; Signal Transduction; Statistics, Nonparametric; Thapsigargin; Transfection; Valine	2012

Article

Year

Substituting c-Jun N-terminal kinase-3 (JNK3) ATP-binding site amino acid residues with their p38 counterparts affects binding of JNK- and p38-selective inhibitors.

Archives of biochemistry and biophysics, 2005, Jun-15, Volume: 438, Issue:2

Topics: Adenosine Triphosphate; Alanine; Amino Acids; Animals; Anthracenes; Binding Sites; Biotinylation; Crystallography, X-Ray; Enzyme Inhibitors; Fluorescence Resonance Energy Transfer; Glutathione; Humans; Imidazoles; Inhibitory Concentration 50; Isoleucine; Kinetics; MAP Kinase Signaling System; Mitogen-Activated Protein Kinase 10; Models, Biological; Models, Chemical; Models, Molecular; Mutation; p38 Mitogen-Activated Protein Kinases; Phosphorylation; Point Mutation; Protein Binding; Protein Folding; Pyrimidines; Valine

2005

Repression of transcription of presenilin-1 inhibits γ-secretase independent ER Ca²⁺ leak that is impaired by FAD mutations.

Journal of neurochemistry, 2012, Volume: 122, Issue:3

Topics: Amyloid Precursor Protein Secretases; Anthracenes; Calcium; Carrier Proteins; Cell Line, Tumor; Cytosol; DNA Helicases; Dose-Response Relationship, Drug; Endoplasmic Reticulum; Enzyme Inhibitors; Gene Expression Regulation, Neoplastic; Humans; Inositol 1,4,5-Trisphosphate Receptors; Methionine; Mi-2 Nucleosome Remodeling and Deacetylase Complex; Mutation; Neuroblastoma; Nuclear Proteins; Peptide Fragments; Presenilin-1; Signal Transduction; Statistics, Nonparametric; Thapsigargin; Transfection; Valine

2012