A myelin gene causative of a catatonia-depression syndrome upon aging.
about
Uncoupling of neuroinflammation from axonal degeneration in mice lacking the myelin protein tetraspanin-2Cortical network dysfunction caused by a subtle defect of myelination.Myelin-specific proteins: a structurally diverse group of membrane-interacting molecules.Single-shot T1 mapping of the corpus callosum: a rapid characterization of fiber bundle anatomy.Clemastine Enhances Myelination in the Prefrontal Cortex and Rescues Behavioral Changes in Socially Isolated Mice.Purines: forgotten mediators in traumatic brain injury.Oligodendroglial TNFR2 Mediates Membrane TNF-Dependent Repair in Experimental Autoimmune Encephalomyelitis by Promoting Oligodendrocyte Differentiation and Remyelination.Microbiota-driven transcriptional changes in prefrontal cortex override genetic differences in social behavior.Role of CNPase in the oligodendrocytic extracellular 2',3'-cAMP-adenosine pathway.The myelin membrane-associated enzyme 2',3'-cyclic nucleotide 3'-phosphodiesterase: on a highway to structure and functionPost-stroke depression and the aging brain.Oligodendrocytes: Myelination and Axonal Support.Phenotype-Based Genetic Association Studies (PGAS)-Towards Understanding the Contribution of Common Genetic Variants to Schizophrenia Subphenotypes.Microglia contribute to normal myelinogenesis and to oligodendrocyte progenitor maintenance during adulthood.Genetic inactivation of PERK signaling in mouse oligodendrocytes: normal developmental myelination with increased susceptibility to inflammatory demyelination.Determinants of ligand binding and catalytic activity in the myelin enzyme 2',3'-cyclic nucleotide 3'-phosphodiesteraseNeurotoxocarosis alters myelin protein gene transcription and expression.Neuroinflammation in white matter tracts of Cnp1 mutant mice amplified by a minor brain injury.Microglia ablation alleviates myelin-associated catatonic signs in mice.Micro(glial)-managing executive function: white matter inflammation drives catatonia.Schizoaffective disorder, catatonia and white matter changes - Revisiting the microglial hypothesis.Genetic dissection of oligodendroglial and neuronal Plp1 function in a novel mouse model of spastic paraplegia type 2.Acetyl-CoA production from pyruvate is not necessary for preservation of myelin.The N-terminal domain of the myelin enzyme 2',3'-cyclic nucleotide 3'-phosphodiesterase: direct molecular interaction with the calcium sensor calmodulin.Discovery and Roles of 2',3'-cAMP in Biological Systems.Confused Connections? Targeting White Matter to Address Treatment Resistant Schizophrenia
P2860
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P2860
A myelin gene causative of a catatonia-depression syndrome upon aging.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
A myelin gene causative of a catatonia-depression syndrome upon aging.
@ast
A myelin gene causative of a catatonia-depression syndrome upon aging.
@en
type
label
A myelin gene causative of a catatonia-depression syndrome upon aging.
@ast
A myelin gene causative of a catatonia-depression syndrome upon aging.
@en
prefLabel
A myelin gene causative of a catatonia-depression syndrome upon aging.
@ast
A myelin gene causative of a catatonia-depression syndrome upon aging.
@en
P2093
P2860
P50
P356
P1476
A myelin gene causative of a catatonia-depression syndrome upon aging.
@en
P2093
Anja Ronnenberg
Anne Kästner
Artem Gurvich
Georg L Wieser
Jens Frahm
Martin Begemann
Nora Hagemeyer
Sabine Hofer
Sandra Goebbels
Sergi Papiol
P2860
P304
P356
10.1002/EMMM.201200230
P577
2012-04-04T00:00:00Z