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.
about
Selective toxicity by HDAC3 in neurons: regulation by Akt and GSK3betaNeuroprotection by histone deacetylase-7 (HDAC7) occurs by inhibition of c-jun expression through a deacetylase-independent mechanismOpposing effects of sirtuins on neuronal survival: SIRT1-mediated neuroprotection is independent of its deacetylase activityFree mRNA in excess upon polysome dissociation is a scaffold for protein multimerization to form stress granules.Isoform-specific toxicity of Mecp2 in postmitotic neurons: suppression of neurotoxicity by FoxG1FoxG1 promotes the survival of postmitotic neurons.Histone deacetylase-1 (HDAC1) is a molecular switch between neuronal survival and deathThe influence of CpG and UpA dinucleotide frequencies on RNA virus replication and characterization of the innate cellular pathways underlying virus attenuation and enhanced replication.Design and synthesis of novel protein kinase R (PKR) inhibitors.Regulation of Neuronal Survival by Nucleophosmin 1 (NPM1) Is Dependent on Its Expression Level, Subcellular Localization, and Oligomerization Status.Small molecule kinase inhibitors alleviate different molecular features of myotonic dystrophy type 1.Small Molecules Which Improve Pathogenesis of Myotonic Dystrophy Type 1.
P2860
Q28565080-230B0A18-BC45-4609-ADBA-B5AD4E2A6EE9Q28568359-B06EF0B7-9F1B-42CC-90AE-1FC1669D4DD5Q33396651-9AC2A36E-903C-4259-B255-D524FD945E78Q33983718-89BCA7CC-EBAD-4FD6-8C1E-D18B4141D31DQ36112113-B5134B43-D441-4E9E-8B5F-B50A04EBFEB8Q36267774-36C053CC-4A48-4B8E-9BD6-70C83B9BA3E1Q36318929-46614B63-7074-4143-A674-F96535C78F49Q38735720-22063C61-44B2-4195-B074-260CCD982046Q38835635-356247C1-9D9C-454C-94B6-8985208B7F6AQ41161869-F8AE5429-F4FE-46D6-BEC7-3B83BAD94109Q42866387-5930FAF8-DF73-4D9C-BAB9-555C6337EE1AQ55240995-6CD9C466-D7CA-4EA5-8760-18954CFD12C4
P2860
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.
description
2008 nî lūn-bûn
@nan
2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@ast
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@en
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@nl
type
label
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@ast
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@en
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@nl
prefLabel
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@ast
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@en
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@nl
P2093
P2860
P1476
A chemical compound commonly u ...... iting cyclin-dependent kinase.
@en
P2093
Hsin-Mei Chen
Santosh R D'Mello
P2860
P304
P356
10.1111/J.1460-9568.2008.06491.X
P407
P577
2008-11-01T00:00:00Z