Disruption of Foxg1 expression by knock-in of cre recombinase: effects on the development of the mouse telencephalon.
about
Conditional gene expression in the mouse inner ear using Cre-loxP.Dynamic FoxG1 expression coordinates the integration of multipolar pyramidal neuron precursors into the cortical plateOrganization of somatosensory cortex in the Northern grasshopper mouse (Onychomys leucogaster), a predatory rodentChanges in the regulation of the Notch signaling pathway are temporally correlated with regenerative failure in the mouse cochleaSp8 and COUP-TF1 reciprocally regulate patterning and Fgf signaling in cortical progenitors.The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.JNK regulates FoxO-dependent autophagy in neuronsHESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrain.FOXG1-Related Disorders: From Clinical Description to Molecular Genetics.Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource.Imbalance of excitatory/inhibitory synaptic protein expression in iPSC-derived neurons from FOXG1(+/-) patients and in foxg1(+/-) miceBeyond knockouts: cre resources for conditional mutagenesis.Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.Foxg1 haploinsufficiency reduces the population of cortical intermediate progenitor cells: effect of increased p21 expression.Expression and actions of transcription factors in adult hippocampal neurogenesis.Epilepsy in Rett syndrome, and CDKL5- and FOXG1-gene-related encephalopathies.In vivo functions of small GTPases in neocortical development.Generation and analysis of an improved Foxg1-IRES-Cre driver mouse line.A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder.FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome.Foxg1 promotes olfactory neurogenesis by antagonizing Gdf11.Altered response to antidepressant treatment in FoxG1 heterozygous knockout mice.Neural deletion of Tgfbr2 impairs angiogenesis through an altered secretome.Cortical and Clonal Contribution of Tbr2 Expressing Progenitors in the Developing Mouse Brain.Utility and limitations of animal models for the functional validation of human sequence variants.Embryonic stem cells neural differentiation qualifies the role of Wnt/β-Catenin signals in human telencephalic specification and regionalization.Transplantation of iPS cell-derived neural progenitors overexpressing SDF-1α increases regeneration and functional recovery after ischemic stroke.RORα Coordinates Thalamic and Cortical Maturation to Instruct Barrel Cortex Development.Sox2 haploinsufficiency primes regeneration and Wnt responsiveness in the mouse cochlea.
P2860
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P2860
Disruption of Foxg1 expression by knock-in of cre recombinase: effects on the development of the mouse telencephalon.
description
2007 nî lūn-bûn
@nan
2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Disruption of Foxg1 expression ...... nt of the mouse telencephalon.
@ast
Disruption of Foxg1 expression ...... nt of the mouse telencephalon.
@en
type
label
Disruption of Foxg1 expression ...... nt of the mouse telencephalon.
@ast
Disruption of Foxg1 expression ...... nt of the mouse telencephalon.
@en
prefLabel
Disruption of Foxg1 expression ...... nt of the mouse telencephalon.
@ast
Disruption of Foxg1 expression ...... nt of the mouse telencephalon.
@en
P2093
P2860
P1433
P1476
Disruption of Foxg1 expression ...... nt of the mouse telencephalon.
@en
P2093
P2860
P304
P356
10.1016/J.NEUROSCIENCE.2007.06.012
P407
P577
2007-07-19T00:00:00Z