(Q42468550)

20220004

1 November 2017

title

Necdin promotes tangential migration of neocortical interneurons from basal forebrain (English)

1 reference

1 November 2017

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

author name string

Koichi Hasegawa

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

Kazuaki Yoshikawa

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

language of work or name

English

0 references

publication date

1 March 2010

1 reference

20220004

1 November 2017

published in

Journal of Neuroscience

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

volume

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

page(s)

3709-3714

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

Disruption of the mouse necdin gene results in early post-natal lethality

15 May 2020

cites work

1 reference

12 December 2020

Cellular and subcellular localization of necdin in fetal and adult mouse brain

1 reference

12 December 2020

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

1 reference

12 December 2020

The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease

1 reference

12 December 2020

Control of cortical interneuron migration by neurotrophins and PI3-kinase signaling.

1 reference

12 December 2020

Cell migration in the forebrain

1 reference

12 December 2020

Model of autism: increased ratio of excitation/inhibition in key neural systems

1 reference

12 December 2020

Necdin interacts with the Msx2 homeodomain protein via MAGE-D1 to promote myogenic differentiation of C2C12 cells

1 reference

12 December 2020

Developmental regulation of gonadotropin-releasing hormone gene expression by the MSX and DLX homeodomain protein families

1 reference

12 December 2020

Behavioural phenotypes of hypomorphic KCC2-deficient mice

1 reference

12 December 2020

Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival

1 reference

12 December 2020

Pervasive developmental disorders in Prader-Willi syndrome: the Leuven experience in 59 subjects and controls.

1 reference

12 December 2020

Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.

1 reference

12 December 2020

Recent assembly of an imprinted domain from non-imprinted components.

1 reference

12 December 2020

Single mage gene in the chicken genome encodes CMage, a protein with functional similarities to mammalian type II Mage proteins.

1 reference

12 December 2020

Dlx2 homeobox gene transcriptional regulation of Trkb neurotrophin receptor expression during mouse retinal development

1 reference

12 December 2020

Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons.

1 reference

12 December 2020

Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons

1 reference

12 December 2020

Arx is a direct target of Dlx2 and thereby contributes to the tangential migration of GABAergic interneurons

1 reference

12 December 2020

Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.

1 reference

12 December 2020

Characteristics and frequency of seizure disorder in 56 patients with Prader-Willi syndrome

1 reference

12 December 2020

The embryonic preoptic area is a novel source of cortical GABAergic interneurons.

1 reference

12 December 2020

A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells

1 reference

12 December 2020

Structure and expression of the mouse necdin gene. Identification of a postmitotic neuron-restrictive core promoter

1 reference

12 December 2020

Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons.

1 reference

12 December 2020

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

1 reference

12 December 2020

Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes

1 reference

12 December 2020

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

1 reference

12 December 2020

The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region

1 reference

12 December 2020

10.1523/JNEUROSCI.5797-09.2010

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6632249&resulttype=core&format=json

15 May 2020

20220004

1 reference