(Q24321498)

GOA release 2020-03-11

cell adhesion

1 reference

GOA release 2020-03-11

1 reference

M Jouet

1

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A Rosenthal

2

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G Armstrong

3

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J MacFarlane

4

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R Stevenson

5

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J Paterson

6

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A Metzenberg

7

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V Ionasescu

8

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K Temple

9

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S Kenwrick

Neurite outgrowth on immobilized axonin-1 is mediated by a heterophilic interaction with L1(G4)

10

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language of work or name

English

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publication date

July 1994

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published in

Nature Genetics

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volume

7

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issue

3

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page(s)

402-7

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0794-402

The MASA syndrome: A new heritable mental retardation syndrome

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Regulation of axonal growth in the vertebrate nervous system by interactions between glycoproteins belonging to two subgroups of the immunoglobulin superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Cell adhesion molecules and their subgroups in the nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

A duplication in the L1CAM gene associated with X-linked hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Calcium influx into neurons can solely account for cell contact-dependent neurite outgrowth stimulated by transfected L1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Neural cell adhesion molecules modulate tyrosine phosphorylation of tubulin in nerve growth cone membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Molecular cloning of cDNA encoding the rat neural cell adhesion molecule L1. Two L1 isoforms in the cytoplasmic region are produced by differential splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Neural adhesion molecule L1 as a member of the immunoglobulin superfamily with binding domains similar to fibronectin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

Complicated hereditary spastic paraparesis with cerebral white matter lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

21 January 2018

X-linked hydrocephalus

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

X-linked mental retardation associated with bilateral clasp thumb anomaly.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Mental retardation-clasped thumb syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

MASA syndrome: further clinical delineation and chromosomal localisation

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

MASA syndrome: new clinical features and linkage analysis using DNA probes

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Assignment of X-linked hydrocephalus to Xq28 by linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Clasped-thumb mental retardation (MASA) syndrome: confirmation of linkage to Xq28.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

MASA syndrome: clinical variability and linkage analysis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Neural cell-to-cell adhesion and recognition

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS)

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Sex-linked hydrocephalus. Report of a family with 15 affected members

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

L1-mediated axon outgrowth occurs via a homophilic binding mechanism

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Neural cell adhesion molecules influence second messenger systems

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

A protein kinase activity is associated with and specifically phosphorylates the neural cell adhesion molecule L1

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Several extracellular domains of the neural cell adhesion molecule L1 are involved in neurite outgrowth and cell body adhesion.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Variants of human L1 cell adhesion molecule arise through alternate splicing of RNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Immunocytochemical localization of cell adhesion molecule L1 in developing rat pyramidal tract

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

L1 mono- and polyclonal antibodies modify cell migration in early postnatal mouse cerebellum

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Detecting single base substitutions as heteroduplex polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Molecular structure and functional testing of human L1CAM: an interspecies comparison

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021

Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulindependent diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNG0794-402

7 January 2021