about
Identification of HS1 protein as a major substrate of protein-tyrosine kinase(s) upon B-cell antigen receptor-mediated signalingANA, a novel member of Tob/BTG1 family, is expressed in the ventricular zone of the developing central nervous systemPSD-95 promotes Fyn-mediated tyrosine phosphorylation of the N-methyl-D-aspartate receptor subunit NR2AReceptor specificity of the fibroblast growth factor family. The complete mammalian FGF familyp250GAP, a novel brain-enriched GTPase-activating protein for Rho family GTPases, is involved in the N-methyl-d-aspartate receptor signalingNegative regulation of BMP/Smad signaling by Tob in osteoblastsHeteromer formation of delta2 glutamate receptors with AMPA or kainate receptorsTob proteins enhance inhibitory Smad-receptor interactions to repress BMP signalingSpecific expressions of Fyn and Lyn, lymphocyte antigen receptor-associated tyrosine kinases, in the central nervous systemThe AMPA receptor interacts with and signals through the protein tyrosine kinase LynDistinct target-derived signals organize formation, maturation, and maintenance of motor nerve terminalsNR2B tyrosine phosphorylation modulates fear learning as well as amygdaloid synaptic plasticityInvolvement of NMDAR2A tyrosine phosphorylation in depression-related behaviour.The protein-tyrosine phosphatase PTPMEG interacts with glutamate receptor delta 2 and epsilon subunits.FGF22 and its close relatives are presynaptic organizing molecules in the mammalian brain.Selective synaptic targeting of the excitatory and inhibitory presynaptic organizers FGF22 and FGF7.Orchestrating the synaptic network by tyrosine phosphorylation signallingDistinct sets of FGF receptors sculpt excitatory and inhibitory synaptogenesis.Fibroblast growth factor 22 contributes to the development of retinal nerve terminals in the dorsal lateral geniculate nucleus.Mice lacking a transcriptional corepressor Tob are predisposed to cancer.Physical and functional association of the cbl protooncogen product with an src-family protein tyrosine kinase, p53/56lyn, in the B cell antigen receptor-mediated signalingSeeking long-term relationship: axon and target communicate to organize synaptic differentiation.Excitability governs neural development in a hippocampal region-specific manner.Deletion of fibroblast growth factor 22 (FGF22) causes a depression-like phenotype in adult mice.Postsynaptic SDC2 induces transsynaptic signaling via FGF22 for bidirectional synaptic formation.Synapse maturation by activity-dependent ectodomain shedding of SIRPα.Weaving the neuronal net with target-derived fibroblast growth factors.A microRNA negative feedback loop downregulates vesicle transport and inhibits fear memory.The best-laid plans go oft awry: synaptogenic growth factor signaling in neuropsychiatric disease.Secreted factors as synaptic organizers.Specific sets of intrinsic and extrinsic factors drive excitatory and inhibitory circuit formation.Activity-dependent proteolytic cleavage of cell adhesion molecules regulates excitatory synaptic development and function.Suppression of epileptogenesis-associated changes in response to seizures in FGF22-deficient mice.FGF22 signaling regulates synapse formation during post-injury remodeling of the spinal cordSrc family tyrosine kinases associate with and phosphorylate CTLA-4 (CD152).NMDAR2B tyrosine phosphorylation regulates anxiety-like behavior and CRF expression in the amygdalaNeurogenesis is enhanced and mossy fiber sprouting arises in FGF7-deficient mice during development.Buttressing a balanced brain: Target-derived FGF signaling regulates excitatory/inhibitory tone and adult neurogenesis within the maturating hippocampal networkSignal regulatory proteins (SIRPS) are secreted presynaptic organizing moleculesMultiple forms of activity-dependent competition refine hippocampal circuits in vivo.
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description
researcher
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wetenschapper
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հետազոտող
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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H Umemori
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P108
P106
P31
P496
0000-0001-7198-2062