about
Activation of TRAP/mediator subunit TRAP220/Med1 is regulated by mitogen-activated protein kinase-dependent phosphorylationThe structure of cyclin H: common mode of kinase activation and specific features.Cdc6 protein causes premature entry into S phase in a mammalian cell-free system.BRCA1 is phosphorylated at serine 1497 in vivo at a cyclin-dependent kinase 2 phosphorylation siteDelta-aminolevulinic acid cytotoxic effects on human hepatocarcinoma cell linesA Novel Approach to the Discovery of Small-Molecule Ligands of CDK2Inhibition of cyclin-dependent kinases by purine analogues: crystal structure of human cdk2 complexed with roscovitineProtein kinase inhibition by staurosporine revealed in details of the molecular interaction with CDK2Cyclin C/CDK8 and cyclin H/CDK7/p36 are biochemically distinct CTD kinasesNaringin-sensitive phosphorylation of plectin, a cytoskeletal cross-linking protein, in isolated rat hepatocytesPfPK6, a novel cyclin-dependent kinase/mitogen-activated protein kinase-related protein kinase from Plasmodium falciparumEstradiol-induced phosphorylation of serine 118 in the estrogen receptor is independent of p42/p44 mitogen-activated protein kinase.Infection of cells with human cytomegalovirus during S phase results in a blockade to immediate-early gene expression that can be overcome by inhibition of the proteasome.Re-oxygenation of hypoxic simian virus 40 (SV40)-infected CV1 cells causes distinct changes of SV40 minichromosome-associated replication proteins.Pneumocystis carinii contains a functional cell-division-cycle Cdc2 homologue.Treatment of Vicia faba root tip cells with specific inhibitors to cyclin-dependent kinases leads to abnormal spindle formation.Roscovitine binds to novel L-channel (CaV1.2) sites that separately affect activation and inactivationEffects of Cell Cycle Regulators on the Cell Cycle Synchronization of Porcine induced Pluripotent Stem Cells.Transcription of herpes simplex virus immediate-early and early genes is inhibited by roscovitine, an inhibitor specific for cellular cyclin-dependent kinasesAnticancer drug targets: cell cycle and checkpoint control.Modulation of apoptosis by the cyclin-dependent kinase inhibitor p27(Kip1)Phosphorylation-dependent degradation of the cyclin-dependent kinase inhibitor p27A novel function of adenovirus E1A is required to overcome growth arrest by the CDK2 inhibitor p27(Kip1).A link between cell cycle and cell death: Bax and Bcl-2 modulate Cdk2 activation during thymocyte apoptosis.Chemical inhibitors: a tool for plant cell cycle studies.A kinase activity associated with simian virus 40 large T antigen phosphorylates upstream binding factor (UBF) and promotes formation of a stable initiation complex between UBF and SL1Flavopiridol, the first cyclin-dependent kinase inhibitor to enter the clinic: current status.Prevention of radiation-induced salivary gland dysfunction utilizing a CDK inhibitor in a mouse modelSelectivity and potency of cyclin-dependent kinase inhibitors.A chemical compound commonly used to inhibit PKR, {8-(imidazol-4-ylmethylene)-6H-azolidino[5,4-g] benzothiazol-7-one}, protects neurons by inhibiting cyclin-dependent kinase.Domain III regulates N-type (CaV2.2) calcium channel closing kineticsPyrimidine and purine analogues, effects on cell cycle regulation and the role of cell cycle inhibitors to enhance their cytotoxicity.Five years of progress on cyclin-dependent kinases and other cellular proteins as potential targets for antiviral drugs.Direct in vivo inhibition of the nuclear cell cycle cascade in experimental mesangial proliferative glomerulonephritis with Roscovitine, a novel cyclin-dependent kinase antagonist.Extremes in rapid cellular morphogenesis: post-transcriptional regulation of spermatogenesis in Marsilea vestita.Expression profiles of a human pancreatic cancer cell line upon induction of apoptosis search for modulators in cancer therapy.Common and reversible regulation of wild-type p53 function and of ribosomal biogenesis by protein kinases in human cells.Potent inhibitors of cyclin-dependent kinase 2 induce nuclear accumulation of wild-type p53 and nucleolar fragmentation in human untransformed and tumor-derived cells.Induction of apoptosis in cancer cells by tumor necrosis factor and butyrolactone, an inhibitor of cyclin-dependent kinases.Two kinase activities are sufficient for sea urchin sperm chromatin decondensation in vitro.
P2860
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P2860
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Chemical inhibitors of cyclin-dependent kinases.
@ast
Chemical inhibitors of cyclin-dependent kinases.
@en
type
label
Chemical inhibitors of cyclin-dependent kinases.
@ast
Chemical inhibitors of cyclin-dependent kinases.
@en
prefLabel
Chemical inhibitors of cyclin-dependent kinases.
@ast
Chemical inhibitors of cyclin-dependent kinases.
@en
P1476
Chemical inhibitors of cyclin-dependent kinases.
@en
P2093
P304
P356
10.1016/0962-8924(96)10034-9
P577
1996-10-01T00:00:00Z