(Q28160539)

10

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author name string

R Ohira

1

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Y H Zhang

2

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W Guo

3

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K Dipple

4

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S L Shih

5

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J Doerr

6

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B L Huang

7

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L J Fu

8

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A Abu-Khalil

9

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E R B McCabe

11

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language of work or name

English

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publication date

2002

1 reference

Molecular Genetics and Metabolism

PubMed

published in

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volume

77

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issue

1-2

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page(s)

179-88

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cites work

Central nervous system neuronal migration

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The brain organization.

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Expression of a novel aristaless related homeobox gene 'Arx' in the vertebrate telencephalon, diencephalon and floor plate

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

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7 January 2021

Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome

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7 January 2021

exma: an X-linked insertional mutation that disrupts forebrain and eye development.

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

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7 January 2021

Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila

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

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

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The mouse Dlx-2 (Tes-1) gene is expressed in spatially restricted domains of the forebrain, face and limbs in midgestation mouse embryos

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7 January 2021

DLX-1, DLX-2, and DLX-5 expression define distinct stages of basal forebrain differentiation

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7 January 2021

Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain

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Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches

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7 January 2021

Cloning and characterization of two members of the vertebrate Dlx gene family

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7 January 2021

Emx1 and Emx2 show different patterns of expression during proliferation and differentiation of the developing cerebral cortex in the mouse.

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

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7 January 2021

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

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Emx and Otx homeobox genes in the developing mouse brain

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Expression patterns of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation

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7 January 2021

Monogenic traits are not simple: lessons from phenylketonuria

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7 January 2021

Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics

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7 January 2021

Modifier genes convert "simple" Mendelian disorders to complex traits

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7 January 2021

Consequences of complexity within biological networks: robustness and health, or vulnerability and disease

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7 January 2021