The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation (Q24535650)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12195014%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation (English)

1 reference

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Severe mental retardation

12 November 2019

main subject

1 reference

7

1 reference

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12 November 2019

author name string

Volker Endris

1

1 reference

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12 November 2019

Birgit Wogatzky

2

1 reference

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12 November 2019

Uwe Leimer

3

1 reference

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12 November 2019

Dusan Bartsch

4

1 reference

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12 November 2019

Malgorzata Zatyka

5

1 reference

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12 November 2019

Farida Latif

6

1 reference

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12 November 2019

Gholamali Tariverdian

8

1 reference

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12 November 2019

Stefan Kirsch

9

1 reference

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12 November 2019

Dieter Karch

10

1 reference

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12 November 2019

Gudrun A Rappold

11

1 reference

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12 November 2019

language of work or name

English

0 references

publication date

23 August 2002

1 reference

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Proceedings of the National Academy of Sciences of the United States of America

12 November 2019

published in

1 reference

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12 November 2019

volume

99

1 reference

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12 November 2019

page(s)

11754-11759

1 reference

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12 November 2019

issue

18

1 reference

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Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation

12 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Detailed mapping of a congenital heart disease gene in chromosome 3p25

24 March 2017

1 reference

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Directional guidance of neuronal migration in the olfactory system by the protein Slit

24 March 2017

1 reference

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A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

An X chromosome-linked gene encoding a protein with characteristics of a rhoGAP predominantly expressed in hematopoietic cells

24 March 2017

1 reference

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Signal transduction in neuronal migration: roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway

24 March 2017

1 reference

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Rich, a rho GTPase-activating protein domain-containing protein involved in signaling by Cdc42 and Rac1

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

CALL gene is haploinsufficient in a 3p- syndrome patient

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Localization of the human caveolin-3 gene to the D3S18/D3S4163/D3S4539 locus (3p25), in close proximity to the human oxytocin receptor gene. Identification of the caveolin-3 gene as a candidate for deletion in 3p-syndrome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Rho GTPases in neuronal morphogenesis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Monogenic causes of X-linked mental retardation.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

A gene for nonsyndromic mental retardation maps to chromosome 3p25-pter

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Genes for cognitive function: developments on the X.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

CdGAP, a novel proline-rich GTPase-activating protein for Cdc42 and Rac.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Mutations in GDI1 are responsible for X-linked non-specific mental retardation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Diversity of cytoplasmic functions for the 3' untranslated region of eukaryotic transcripts.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Molecular genetic analysis of the 3p- syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Mind the GAP, Rho, Rab and GDI.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Clinical and molecular analyses of deletion 3p25-pter syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Purification of recombinant Rho/Rac/G25K from Escherichia coli.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

MECP2 is highly mutated in X-linked mental retardation.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

Rho proteins and the cellular mechanisms of mental retardation.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=129341

A Patient With a Partial Deletion of the Short Arm of Chromosome 3

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12195014

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.162241099

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12195014%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

ADS bibcode

2002PNAS...9911754E

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12195014%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

2 references