(Q37483259)

English

Combination of linkage mapping and microarray-expression analysis identifies NF-kappaB signaling defect as a cause of autosomal-recessive mental retardation

scientific article published on December 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Combination of linkage mapping and microarray-expression analysis identifies NF-kappaB signaling defect as a cause of autosomal-recessive mental retardation (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1 reference

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inferred from title

Christine Bôle-Feysot

8

object named as

Christine Bole-Feysot

0 references

Patrick Nitschké

9

object named as

Patrick Nitschke

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object named as

Asma Smahi

10

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Laurence Colleaux

object named as

Laurence Colleaux

12

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Nathalie Boddaert

object named as

Nathalie Boddaert

7

0 references

11

object named as

Arnold Munnich

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Orianne Philippe

1

object named as

Orianne Philippe

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Florence Molinari

6

object named as

Florence Molinari

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

author name string

Marlène Rio

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Astrid Carioux

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Jean-Marc Plaza

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Philippe Guigue

5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Patrick Nitschke

9

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

1 December 2009

1 reference

Europe PubMed Central

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20 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

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20 August 2017

85

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Europe PubMed Central

PMC publication ID

20 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

903-908

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

A defect in the TUSC3 gene is associated with autosomal recessive mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

IkappaB kinase complexes: gateways to NF-kappaB activation and transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Introduction to NF-kappaB: players, pathways, perspectives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Evolutionarily-conserved role of the NF-kappaB transcription factor in neural plasticity and memory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

NF-kappaB functions in the nervous system: from development to disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

NFkappaB pathway: a good signaling paradigm and therapeutic target

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

NF-kappaB regulates spatial memory formation and synaptic plasticity through protein kinase A/CREB signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

The NF-kappaB pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Signaling between glia and neurons: focus on synaptic plasticity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

NIBP, a novel NIK and IKK(beta)-binding protein that enhances NF-(kappa)B activation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Differential regulation of AMPA receptor and GABA receptor trafficking by tumor necrosis factor-alpha

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Local-pooled-error test for identifying differentially expressed genes with a small number of replicated microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Missing pieces in the NF-kappaB puzzle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Control of synaptic strength by glial TNFalpha

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Evidence for the involvement of TNF and NF-kappaB in hippocampal synaptic plasticity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Nuclear translocation of NF-kappaB is increased in dopaminergic neurons of patients with parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Transcription factor NF-kappaB is activated in primary neurons by amyloid beta peptides and in neurons surrounding early plaques from patients with Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

23 August 2017

Activation of the IkappaB kinase complex and nuclear factor-kappaB contributes to mutant huntingtin neurotoxicity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

14 September 2017

The prevalence of mental retardation: a critical review of recent literature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

28 September 2017

Tumor necrosis factor alters synaptic transmission in rat hippocampal slices

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

26 June 2018

A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

2 September 2018

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

2 September 2018

Activation of the transcription factor NF-kappaB in Schwann cells is required for peripheral myelin formation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

2 September 2018

Truncating neurotrypsin mutation in autosomal recessive nonsyndromic mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

2 September 2018

A requirement of nuclear factor-kappaB activation in fear-potentiated startle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2795800

2 September 2018

Identifiers

10.1016/J.AJHG.2009.11.007

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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