(Q33851469)

29 July 2017

title

Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects (English)

1 reference

29 July 2017

1 reference

Tiziano Pramparo

1

1 reference

29 July 2017

Ondrej Libiger

2

1 reference

29 July 2017

Sonia Jain

3

1 reference

29 July 2017

Hong Li

4

1 reference

29 July 2017

Yong Ha Youn

5

1 reference

29 July 2017

Shinji Hirotsune

6

1 reference

29 July 2017

Nicholas J Schork

7

1 reference

29 July 2017

Anthony Wynshaw-Boris

8

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29 July 2017

publication date

10 March 2011

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29 July 2017

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29 July 2017

volume

7

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29 July 2017

issue

3

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29 July 2017

page(s)

e1001331

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Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

10 March 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

Cytoscape

1 reference

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

based on heuristic

inferred from PubMed Central ID database lookup

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3053345/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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5 July 2018

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5 July 2018

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Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality

5 July 2018

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5 July 2018

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Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration

5 July 2018

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5 July 2018

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RNAi reveals doublecortin is required for radial migration in rat neocortex

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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29 October 2018

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5 July 2018

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5 July 2018

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5 July 2018

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The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors

5 July 2018

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

5 July 2018

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

5 July 2018

1 reference

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

5 July 2018

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

5 July 2018

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Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053345

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053345

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5 July 2018

1 reference

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053345

A multipotent EGF-responsive striatal embryonic progenitor cell produces neurons and astrocytes.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053345

Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division.

5 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

Modulation of T cell development and activation by novel members of the Schlafen (slfn) gene family harbouring an RNA helicase-like motif.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

QN1/KIAA1009: a new essential protein for chromosome segregation and mitotic spindle assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

Characterization of neuroprogenitor cells expressing the PDGF beta-receptor within the subventricular zone of postnatal mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001331

Doublecortin is required in mice for lamination of the hippocampus but not the neocortex.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053345

10.1371/JOURNAL.PGEN.1001331

29 October 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference

29 July 2017

1 reference