(Q48367121)

11 February 2018

title

Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency. (English)

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11 February 2018

author

Fiona Francis

15

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11 February 2018

Marc Dhenain

object named as

Marc Dhenain

2

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Catherine Fallet-Bianco

6

object named as

Catherine Fallet-Bianco

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11 February 2018

author name string

Caroline Kappeler

1

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11 February 2018

Françoise Phan Dinh Tuy

3

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11 February 2018

Yoann Saillour

4

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11 February 2018

Serge Marty

5

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11 February 2018

Isabelle Souville

7

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11 February 2018

Evelyne Souil

8

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11 February 2018

Jean-Marc Pinard

9

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11 February 2018

Gundela Meyer

10

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11 February 2018

Ferechté Encha-Razavi

11

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11 February 2018

Andreas Volk

12

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11 February 2018

Cherif Beldjord

13

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11 February 2018

Jamel Chelly

14

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11 February 2018

language of work or name

English

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publication date

1 January 2007

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11 February 2018

The Journal of Comparative Neurology

published in

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11 February 2018

volume

500

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11 February 2018

page(s)

239-254

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11 February 2018

issue

2

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11 February 2018

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

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Prolonged sojourn of developing pyramidal cells in the intermediate zone of the hippocampus and their settling in the stratum pyramidale.

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doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

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Genotypically defined lissencephalies show distinct pathologies

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7 January 2021

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

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7 January 2021

Multiple dose-dependent effects of Lis1 on cerebral cortical development

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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Kinesin superfamily protein 2A (KIF2A) functions in suppression of collateral branch extension.

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7 January 2021

Doublecortin, a stabilizer of microtubules

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7 January 2021

Corpus callosum deficiency in transgenic mice expressing a truncated ephrin-A receptor.

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7 January 2021

Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice.

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7 January 2021

Axons of early generated neurons in cingulate cortex pioneer the corpus callosum.

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7 January 2021

Doublecortin maintains bipolar shape and nuclear translocation during migration in the adult forebrain

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7 January 2021

Doublecortin-like kinase functions with doublecortin to mediate fiber tract decussation and neuronal migration

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7 January 2021

Malformations of the midline commissures: MRI findings in different forms of callosal dysgenesis.

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7 January 2021

Callosal axon guidance defects in p35(-/-) mice

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7 January 2021

The effect of absence of the corpus callosum on the position of the hippocampus and on the formation of Probst's bundle

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7 January 2021

Multiple Eph receptors and B-class ephrins regulate midline crossing of corpus callosum fibers in the developing mouse forebrain.

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7 January 2021

Selective expression of doublecortin and LIS1 in developing human cortex suggests unique modes of neuronal movement

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Patterns of hippocampal abnormalities in malformations of cortical development

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Reelin promotes hippocampal dendrite development through the VLDLR/ApoER2-Dab1 pathway

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7 January 2021

Topography of interhemispheric connections in neocortex of mice with congenital deficiencies of the callosal commissure

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7 January 2021

Mutation of the Emx-1 homeobox gene disrupts the corpus callosum

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7 January 2021

Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human

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Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system

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The glial sling is a migratory population of developing neurons

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7 January 2021

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Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

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Detailed field pattern is intrinsic to the embryonic mouse hippocampus early in neurogenesis.

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7 January 2021

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

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7 January 2021

Deficiency of corpus callosum varies with strain and supplier of the mice.

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7 January 2021

Mode of inheritance of deficient corpus callosum in mice

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7 January 2021

Abnormal morphological and functional organization of the hippocampus in a p35 mutant model of cortical dysplasia associated with spontaneous seizures.

1 reference

7 January 2021

Identifiers

DOI

10.1002/CNE.21170

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11 February 2018

PubMed ID

17111359

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11 February 2018