(Q28207647)

X-linked lissencephaly with abnormal genitalia

GOA release 2020-03-11

1 reference

William B Dobyns

19

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Mitsuhiro Kato

object named as

Mitsuhiro Kato

18

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Tsutomu Ogata

object named as

Tsutomu Ogata

15

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author name string

Kunio Kitamura

1

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Masako Yanazawa

2

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Noriyuki Sugiyama

3

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Hirohito Miura

4

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Akiko Iizuka-Kogo

5

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Masatomo Kusaka

6

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Kayo Omichi

7

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Rika Suzuki

8

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Yuko Kato-Fukui

9

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Kyoko Kamiirisa

10

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Mina Matsuo

11

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Shin-ichi Kamijo

12

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Megumi Kasahara

13

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Hidefumi Yoshioka

14

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Takayuki Fukuda

16

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Ikuko Kondo

17

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Minesuke Yokoyama

20

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Ken-ichirou Morohashi

New directions for neuronal migration

21

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language of work or name

English

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publication date

November 2002

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published in

Nature Genetics

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volume

32

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issue

3

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page(s)

359-69

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cites work

1 reference

X-linked malformations of cortical development

21 January 2018

1 reference

21 January 2018

1 reference

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 January 2018

1 reference

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

21 January 2018

1 reference

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

21 January 2018

1 reference

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

21 January 2018

1 reference

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly

21 January 2018

1 reference

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

21 January 2018

1 reference

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

21 January 2018

1 reference

Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization

21 January 2018

1 reference

21 January 2018

1 reference

Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1

21 January 2018

1 reference

LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome

21 January 2018

1 reference

Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons

21 January 2018

1 reference

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons

21 January 2018

1 reference

Central nervous system neuronal migration

21 January 2018

1 reference

Differential origins of neocortical projection and local circuit neurons: role of Dlx genes in neocortical interneuronogenesis

21 January 2018

1 reference

Induction and dorsoventral patterning of the telencephalon

21 January 2018

1 reference

The origin and migration of cortical neurones: new vistas

21 January 2018

1 reference

Sorting of striatal and cortical interneurons regulated by semaphorin-neuropilin interactions

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

21 January 2018

1 reference

Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination

21 January 2018

1 reference

Glutamine repeats and neurodegeneration

21 January 2018

1 reference

Origin of GABAergic neurons in the human neocortex

21 January 2018

1 reference

21 January 2018

The battle of the sexes

1 reference

Testosterone formation and metabolism during male sexual differentiation in the human embryo

21 January 2018

1 reference

Adrenocortical and gonadal expression of the mammalian Ftz-F1 gene encoding Ad4BP/SF-1 is independent of pituitary control

21 January 2018

1 reference

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

21 January 2018

1 reference

X-linked lissencephaly with ambiguous genitalia: delineation of further case

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Origin and molecular specification of striatal interneurons.

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Dax-1 as one of the target genes of Ad4BP/SF-1

1 reference