(Q28263735)

English

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

scientific article

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

0 references

0 references

Samuel Berkovic

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Ingrid Scheffer

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

William B. Dobyns

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

author name string

J G Gleeson

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

K M Allen

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

J W Fox

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

E D Lamperti

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

E C Cooper

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

S R Minnerath

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

M E Ross

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

C A Walsh

11

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

language of work or name

0 references

publication date

1 January 1998

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

92

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

63-72

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Identification of a mouse p21Cdc42/Rac activated kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

NCAM-dependent neurite outgrowth is inhibited in neurons from Fyn-minus mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

NCAM140 interacts with the focal adhesion kinase p125(fak) and the SRC-related tyrosine kinase p59(fyn)

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

The spleen protein-tyrosine kinase TPK-IIB is highly similar to the catalytic domain of p72syk

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

A protein related to extracellular matrix proteins deleted in the mouse mutant reeler

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Lissencephaly and other malformations of cortical development: 1995 update

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Causal heterogeneity in isolated lissencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked malformations of neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Dosage-sensitive modifiers of Drosophila abl tyrosine kinase function: prospero, a regulator of axonal outgrowth, and disabled, a novel tyrosine kinase substrate.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mena, a relative of VASP and Drosophila Enabled, is implicated in the control of microfilament dynamics

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mouse disabled (mDab1): a Src binding protein implicated in neuronal development

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Impaired neurite outgrowth of src-minus cerebellar neurons on the cell adhesion molecule L1.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning of a new member of the p21-Cdc42/Rac-activated kinase (PAK) family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Determination of the specific substrate sequence motifs of protein kinase C isozymes

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patie

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Calcium influx induces neurite growth through a Src-Ras signaling cassette

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Mice homozygous for the ablm1 mutation show poor viability and depletion of selected B and T cell populations

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Human p21-activated kinase (Pak1) regulates actin organization in mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

BCM Search Launcher--an integrated interface to molecular biology data base search and analysis services available on the World Wide Web.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Catalytic specificity of protein-tyrosine kinases is critical for selective signalling

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

pp59fyn mutant mice display differential signaling in thymocytes and peripheral T cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980899-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0092-8674(00)80899-5

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9489700%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28263735&oldid=1725021860"