(Q30639738)

13 September 2017

Increased LIS1 expression affects human and mouse brain development (English)

1 reference

13 September 2017

26

1 reference

13 September 2017

Feng Zhang

4

0 references

James R. Lupski

25

object named as

James R Lupski

1 reference

13 September 2017

22

Sau Wai Cheung

1 reference

13 September 2017

Weimin Bi

1

1 reference

13 September 2017

Tamar Sapir

2

1 reference

13 September 2017

Oleg A Shchelochkov

3

1 reference

13 September 2017

Marjorie A Withers

5

1 reference

13 September 2017

Jill V Hunter

6

1 reference

13 September 2017

Talia Levy

7

1 reference

13 September 2017

Vera Shinder

8

1 reference

13 September 2017

Daniel A Peiffer

9

1 reference

13 September 2017

Kevin L Gunderson

10

1 reference

13 September 2017

Marjan M Nezarati

11

1 reference

13 September 2017

Vern Ann Shotts

12

1 reference

13 September 2017

Stephen S Amato

13

1 reference

13 September 2017

Sarah K Savage

14

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13 September 2017

David J Harris

15

1 reference

13 September 2017

Debra-Lynn Day-Salvatore

16

1 reference

13 September 2017

Michele Horner

17

1 reference

13 September 2017

Xin-Yan Lu

18

1 reference

13 September 2017

Trilochan Sahoo

19

1 reference

13 September 2017

Yuchio Yanagawa

20

1 reference

13 September 2017

Arthur L Beaudet

21

1 reference

13 September 2017

language of work or name

English

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publication date

11 January 2009

1 reference

13 September 2017

1 reference

13 September 2017

41

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13 September 2017

2

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13 September 2017

168-177

1 reference

Large recurrent microdeletions associated with schizophrenia

13 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Rare chromosomal deletions and duplications increase risk of schizophrenia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Strong association of de novo copy number mutations with sporadic schizophrenia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Nudel binds Cdc42GAP to modulate Cdc42 activity at the leading edge of migrating cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Association between microdeletion and microduplication at 16p11.2 and autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Recurrent 16p11.2 microdeletions in autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Genomic rearrangements and sporadic disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Strong association of de novo copy number mutations with autism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Cdc42 deficiency causes Sonic hedgehog-independent holoprosencephaly

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Lissencephaly 1 linking to multiple diseases: mental retardation, neurodegeneration, schizophrenia, male sterility, and more

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

The Rho-GTPase cdc42 regulates neural progenitor fate at the apical surface

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

A schizophrenia-associated mutation of DISC1 perturbs cerebral cortex development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

A developmental and genetic classification for malformations of cortical development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Molecular motors in neuronal development, intracellular transport and diseases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Activation of a Dab1/CrkL/C3G/Rap1 pathway in Reelin-stimulated neurons

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Interaction of reelin signaling and Lis1 in brain development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Disregulated RhoGTPases and Actin Cytoskeleton Contribute to the Migration Defect in Lis1-Deficient Neurons

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

LIS1, CLIP-170's key to the dynein/dynactin pathway

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Crk family adaptors-signalling complex formation and biological roles

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

The structural basis for red fluorescence in the tetrameric GFP homolog DsRed

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Targeting of cre to the Foxg1 (BF-1) locus mediates loxP recombination in the telencephalon and other developing head structures

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Characterization of rac and cdc42 activation in chemoattractant-stimulated human neutrophils using a novel assay for active GTPases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4396744

Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2).

20 June 2018

1 reference

Partial trisomy 17p detected by spectral karyotyping.

21 January 2018

1 reference

Intrinsic polarity of mammalian neuroepithelial cells

21 January 2018

1 reference

Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67-GFP knock-in mouse.

21 January 2018

1 reference

Interaction between Dab1 and CrkII is promoted by Reelin signaling

21 January 2018

1 reference

Dynein binds to beta-catenin and may tether microtubules at adherens junctions.

21 January 2018

1 reference

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

21 January 2018

1 reference

Z/AP, a double reporter for cre-mediated recombination.

21 January 2018

1 reference

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19136950

12 December 2020

inferred from PubMed ID database lookup

Ndel1 operates in a common pathway with LIS1 and cytoplasmic dynein to regulate cortical neuronal positioning

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19136950

12 December 2020

inferred from PubMed ID database lookup

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19136950

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/NG.302

1 reference

release_ymv2xshn75atre2qpcfan2yepi

13 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ymv2xshn75atre2qpcfan2yepi

24 November 2022

mapped directly with Wikidata item

1 reference

13 September 2017

PubMed publication ID

19136950

1 reference