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Immunocytochemical localization of a neuron-specific diacylglycerol kinase beta and gamma in the developing rat brainEffect of trehalose on the properties of mutant {gamma}PKC, which causes spinocerebellar ataxia type 14, in neuronal cell lines and cultured Purkinje cells.Elucidation of the molecular mechanism and exploration of novel therapeutics for spinocerebellar ataxia caused by mutant protein kinase Cγ.Deregulation of the actin cytoskeleton and macropinocytosis in response to phorbol ester by the mutant protein kinase C gamma that causes spinocerebellar ataxia type 14.Loss of the Phenolic Hydroxyl Group and Aromaticity from the Side Chain of Anti-Proliferative 10-Methyl-aplog-1, a Simplified Analog of Aplysiatoxin, Enhances Its Tumor-Promoting and Proinflammatory Activities.Xeroderma pigmentosum group C protein interacts with histones: regulation by acetylated states of histone H3.Mutant γPKC that causes spinocerebellar ataxia type 14 upregulates Hsp70, which protects cells from the mutant's cytotoxicity.Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy.S-Palmitoylation of a Novel Site in the β2-Adrenergic Receptor Associated with a Novel Intracellular ItineraryDiacylglycerol kinase beta accumulates on the perisynaptic site of medium spiny neurons in the striatum.Importance of chroman ring and tyrosine phosphorylation in the subtype-specific translocation and activation of diacylglycerol kinase alpha by D-alpha-tocopherol.The Role of Cysteine String Protein α Phosphorylation at Serine 10 and 34 by Protein Kinase Cγ for Presynaptic Maintenance.The role of Pak-interacting exchange factor-β phosphorylation at serines 340 and 583 by PKCγ in dopamine release.Mutant gammaPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells.Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death.Enzymological analysis of mutant protein kinase Cgamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis.Propofol induced diverse and subtype-specific translocation of PKC families.Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein.Differential S-palmitoylation of the human and rodent β3-adrenergic receptorsPharmacological induction of heat shock proteins ameliorates toxicity of mutant PKCγ in spinocerebellar ataxia type 14
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Q28582440-5C006058-7EE8-419F-9E3A-30760DA89825Q30497111-F8C6A3CC-C725-4F0C-89C6-225A09313D37Q37888367-D53FEC80-F2AF-48C2-A3F3-612EE61C1D30Q38642817-E0A0470B-7457-4DAF-8E44-78E349E41EC6Q38707861-29F0A092-89EF-4EB7-82DC-AFBB8D70C5BDQ38715086-4271669A-E1D7-4305-B3F1-84B4284318CCQ39097836-7B032891-9463-4FE5-82CA-05B369E9A6C0Q39714056-F94AE897-3BA6-41F9-89EC-3073F1D02997Q41107029-E016B38B-CE4B-4F02-B54A-7640B554B189Q46195666-483360A3-80EA-427E-85F7-721C02DD80B2Q46386464-9992A0B3-11B8-4769-BED7-03A4E00DA59FQ47372346-90A5BBCC-AF8D-422B-BB12-CF32D056EA79Q48291439-087C3373-51B0-4E8B-8296-17172944EA5FQ50611131-2F9B491D-BD68-4638-AE15-D8DC2282991EQ50764411-D38C8628-30F5-4662-A552-5E39546F7A7CQ51788908-84461DCC-FCB0-4A2E-A532-87F1B66C5DB6Q54114087-C8612D1E-FCB9-4D98-9A5C-D0AEB302C55AQ54322709-C867D4BC-3CE7-4D80-A58A-1957242E3F6BQ90437347-5440B419-1340-4927-9E1D-E10DE6ACD867Q90858543-887243DA-1F97-4FB5-B7FB-E1CCC9A86EEC
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description
Forscher
@de
investigador
@es
researcher
@en
ricercatore
@it
wetenschapper
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հետազոտող
@hy
研究者
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name
Naoko Adachi
@ast
Naoko Adachi
@en
Naoko Adachi
@es
Naoko Adachi
@nl
type
label
Naoko Adachi
@ast
Naoko Adachi
@en
Naoko Adachi
@es
Naoko Adachi
@nl
prefLabel
Naoko Adachi
@ast
Naoko Adachi
@en
Naoko Adachi
@es
Naoko Adachi
@nl
P106
P108
P31
P496
0000-0002-8797-0717