about
Genetic transformation of Indian bread (T. aestivum) and pasta (T. durum) wheat by particle bombardment of mature embryo-derived calliFunctional analysis of the N- and C-terminus of mammalian G9a histone H3 methyltransferaseStructure and functional characterization of the atypical human kinase haspinInhibitors of Glycogen Synthase Kinase 3 with Exquisite Kinome-Wide Selectivity and Their Functional EffectsIdentification of small molecule inhibitors of the mitotic kinase haspin by high-throughput screening using a homogeneous time-resolved fluorescence resonance energy transfer assay.A positive feedback loop involving Haspin and Aurora B promotes CPC accumulation at centromeres in mitosisPerturbation of mitosis through inhibition of histone acetyltransferases: the key to ochratoxin a toxicity and carcinogenicity?Brain-penetrant LSD1 inhibitors can block memory consolidation.Haspin inhibitors reveal centromeric functions of Aurora B in chromosome segregationDual histone H3 methylation marks at lysines 9 and 27 required for interaction with CHROMOMETHYLASE3.Dissecting structure-activity-relationships of crebinostat: Brain penetrant HDAC inhibitors for neuroepigenetic regulation.Catalytic properties and kinetic mechanism of human recombinant Lys-9 histone H3 methyltransferase SUV39H1: participation of the chromodomain in enzymatic catalysis.Discovery of a Highly Selective Glycogen Synthase Kinase-3 Inhibitor (PF-04802367) That Modulates Tau Phosphorylation in the Brain: Translation for PET Neuroimaging.Structure-activity relationship study of acridine analogs as haspin and DYRK2 kinase inhibitors.Structure-activity relationship study of beta-carboline derivatives as haspin kinase inhibitors.Sequence specificity and role of proximal amino acids of the histone H3 tail on catalysis of murine G9A lysine 9 histone H3 methyltransferase.Development of [18F]Maleimide-Based Glycogen Synthase Kinase-3β Ligands for Positron Emission Tomography Imaging.Targeting the SET and RING-associated (SRA) domain of ubiquitin-like, PHD and ring finger-containing 1 (UHRF1) for anti-cancer drug development.Dual histone H3 methylation marks at lysines 9 and 27 required for interaction with CHROMOMETHYLASE3.Discovery of suppressors of CRMP2 phosphorylation reveals compounds that mimic the behavioral effects of lithium on amphetamine-induced hyperlocomotionHDAC1 modulates OGG1-initiated oxidative DNA damage repair in the aging brain and Alzheimer's diseaseStructure-based screening of chemical libraries to identify small molecules that are likely to bind with the SET and RING-associated (SRA) domain of Ubiquitin-like, PHD and Ring Finger-containing 1 (UHRF1)
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Debasis Patnaik
@ast
Debasis Patnaik
@en
Debasis Patnaik
@es
Debasis Patnaik
@nl
type
label
Debasis Patnaik
@ast
Debasis Patnaik
@en
Debasis Patnaik
@es
Debasis Patnaik
@nl
prefLabel
Debasis Patnaik
@ast
Debasis Patnaik
@en
Debasis Patnaik
@es
Debasis Patnaik
@nl
P106
P1153
6603054846
P31
P496
0000-0002-9829-3352