(Q34349426)

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Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons (English)

1 reference

Europe PubMed Central

1 August 2017

neural stem cell

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

1 August 2017

object named as

Vania Broccoli

5

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author name string

Elena Colombo

1

1 reference

Europe PubMed Central

1 August 2017

Rossella Galli

2

1 reference

Europe PubMed Central

1 August 2017

Giulio Cossu

3

1 reference

Europe PubMed Central

1 August 2017

publication date

1 November 2004

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Europe PubMed Central

1 August 2017

Developmental Dynamics

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Europe PubMed Central

1 August 2017

231

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Europe PubMed Central

1 August 2017

631-639

1 reference

Europe PubMed Central

1 August 2017

3

1 reference

Europe PubMed Central

1 August 2017

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Regulation of area identity in the mammalian neocortex by Emx2 and Pax6.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Dorsal-ventral patterning in the mammalian telencephalon

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Monogenic causes of X-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Three distinct families of GABAergic neurons in rat visual cortex.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Lissencephaly and the molecular basis of neuronal migration

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Neurogenesis and neuronal migration in the neonatal rat forebrain anterior subventricular zone do not require GFAP-positive astrocytes.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Loss of Emx2 function leads to ectopic expression of Wnt1 in the developing telencephalon and cortical dysplasia.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Restricted proliferation and migration of postnatally generated neurons derived from the forebrain subventricular zone

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Area identity shifts in the early cerebral cortex of Emx2-/- mutant mice.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

A long, remarkable journey: tangential migration in the telencephalon.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Directional guidance of interneuron migration to the cerebral cortex relies on subcortical Slit1/2-independent repulsion and cortical attraction

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Channelopathies as a genetic cause of epilepsy

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Nested expression domains of four homeobox genes in developing rostral brain

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Potential mechanisms of mutations that affect neuronal migration in man and mouse

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Permissive corridor and diffusible gradients direct medial ganglionic eminence cell migration to the neocortex

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

21 January 2018

Regional and cellular patterns of reelin mRNA expression in the forebrain of the developing and adult mouse.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

7 January 2021

based on heuristic

inferred from DOI database lookup

Neurogenesis in adult subventricular zone.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

7 January 2021

based on heuristic

inferred from DOI database lookup

The Xenopus arx gene is expressed in the developing rostral forebrain.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

7 January 2021

based on heuristic

inferred from DOI database lookup

The lack of Emx2 causes impairment of Reelin signaling and defects of neuronal migration in the developing cerebral cortex

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of two distinct progenitor populations in the lateral ganglionic eminence: implications for striatal and olfactory bulb neurogenesis.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20164

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/DVDY.20164

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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