(Q41938609)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020049%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53 (English)

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17 January 2020

5

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17 January 2020

author name string

Claudia Seah

1

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17 January 2020

Michael A Levy

2

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17 January 2020

Yan Jiang

3

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17 January 2020

Sulayman Mokhtarzada

4

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17 January 2020

Richard J Gibbons

6

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17 January 2020

Nathalie G Bérubé

7

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17 January 2020

language of work or name

English

0 references

publication date

1 November 2008

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17 January 2020

published in

Journal of Neuroscience

1 reference

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17 January 2020

volume

28

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17 January 2020

issue

47

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17 January 2020

page(s)

12570-12580

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Neural precursor cells differentiating in the absence of Rb exhibit delayed terminal mitosis and deregulated E2F 1 and 3 activity.

17 January 2020

cites work

1 reference

12 December 2020

A class of neuroD-related basic helix-loop-helix transcription factors expressed in developing central nervous system in zebrafish

1 reference

12 December 2020

Carpenter-Waziri syndrome results from a mutation in XNP

1 reference

12 December 2020

Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation bias

1 reference

12 December 2020

Hippocampus development and generation of dentate gyrus granule cells is regulated by LEF1

1 reference

12 December 2020

Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy

1 reference

12 December 2020

Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

1 reference

12 December 2020

Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome

1 reference

12 December 2020

Neuronal basic helix-loop-helix proteins (NEX and BETA2/Neuro D) regulate terminal granule cell differentiation in the hippocampus

1 reference

12 December 2020

Structure of the mouse NDRF gene and its regulation during neuronal differentiation of P19 cells

1 reference

12 December 2020

Targeting of cre to the Foxg1 (BF-1) locus mediates loxP recombination in the telencephalon and other developing head structures

1 reference

12 December 2020

Unique expression patterns of cell fate molecules delineate sequential stages of dentate gyrus development.

1 reference

12 December 2020

Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems

1 reference

12 December 2020

Cell migration from the ganglionic eminences is required for the development of hippocampal GABAergic interneurons

1 reference

12 December 2020

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

1 reference

12 December 2020

On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models

1 reference

12 December 2020

Differential regulation of basic helix-loop-helix mRNAs in the dentate gyrus following status epilepticus

1 reference

12 December 2020

Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.

1 reference

12 December 2020

Linkage analysis of X-linked nuclear protein gene in Smith-Fineman-Myers syndrome

1 reference

12 December 2020

Abnormal development of the hippocampal dentate gyrus in mice lacking the CXCR4 chemokine receptor

1 reference

12 December 2020

Altered synaptic plasticity in a mouse model of fragile X mental retardation

1 reference

12 December 2020

The chemokine SDF1 regulates migration of dentate granule cells

1 reference

12 December 2020

Coffin-Lowry syndrome: clinical and molecular features

1 reference

12 December 2020

BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus.

1 reference

12 December 2020

Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein-Taybi syndrome

1 reference

12 December 2020

Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome.

1 reference

12 December 2020

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

1 reference

12 December 2020

The recurrent mossy fiber pathway of the epileptic brain

1 reference

12 December 2020

Cockayne syndrome group B cellular and biochemical functions

1 reference

12 December 2020

Wnt signaling mutants have decreased dentate granule cell production and radial glial scaffolding abnormalities

1 reference

12 December 2020

bHLH gene expression in the Emx2-deficient dentate gyrus reveals defective granule cells and absence of migrating precursors

1 reference

12 December 2020

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis

1 reference

12 December 2020

Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy

1 reference

12 December 2020

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues

1 reference

12 December 2020

Lhx6 activity is required for the normal migration and specification of cortical interneuron subtypes

1 reference

12 December 2020

Loss of ATRX leads to chromosome cohesion and congression defects

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12 December 2020

Mosaic organization of the hippocampal neuroepithelium and the multiple germinal sources of dentate granule cells

1 reference

12 December 2020

Migration and distribution of two populations of hippocampal granule cell precursors during the perinatal and postnatal periods

1 reference

12 December 2020

A mouse model for Down syndrome exhibits learning and behaviour deficits.

1 reference

12 December 2020

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1 reference

12 December 2020

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

1 reference

12 December 2020

The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons.

1 reference

12 December 2020

The functional organization of the hippocampal dentate gyrus and its relevance to the pathogenesis of temporal lobe epilepsy

1 reference

12 December 2020

XNP mutation in a large family with Juberg-Marsidi syndrome

1 reference

12 December 2020

A role for Cajal-Retzius cells and reelin in the development of hippocampal connections.

1 reference

12 December 2020

Dentate gyrus formation requires Emx2

1 reference

12 December 2020

More hippocampal neurons in adult mice living in an enriched environment

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12 December 2020

Disruption of hippocampal development in vivo by CR-50 mAb against reelin

1 reference

12 December 2020

Genetic influence on neurogenesis in the dentate gyrus of adult mice

1 reference

12 December 2020

Regulated expression of neurogenic basic helix-loop-helix transcription factors during differentiation of the immortalized neuronal progenitor cell line HC2S2 into neurons

1 reference

12 December 2020

Environmental stimulation of 129/SvJ mice causes increased cell proliferation and neurogenesis in the adult dentate gyrus

1 reference

12 December 2020

Multipotent progenitor cells in the adult dentate gyrus.

1 reference

12 December 2020

Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations

1 reference

12 December 2020

10.1523/JNEUROSCI.4048-08.2008

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020049%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020049%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

PubMed publication ID

19020049

1 reference