(Q34660147)

3 August 2017

title

Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin-Lowry syndrome (English)

1 reference

3 August 2017

main subject

Coffin-Lowry syndrome

1 reference

7

Allan L Reiss

1 reference

3 August 2017

Shelli R Kesler

1

1 reference

3 August 2017

Richard J Simensen

2

1 reference

3 August 2017

Kytja Voeller

3

1 reference

3 August 2017

Fatima Abidi

4

1 reference

3 August 2017

Roger E Stevenson

5

1 reference

3 August 2017

Charles E Schwartz

6

1 reference

3 August 2017

publication date

22 February 2007

1 reference

3 August 2017

1 reference

3 August 2017

volume

8

1 reference

3 August 2017

issue

2

1 reference

3 August 2017

page(s)

143-147

1 reference

https://scigraph.springernature.com/pub.10.1007/s10048-007-0080-6

3 August 2017

exact match

0 references

cites work

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The movement disorders of Coffin-Lowry syndrome

7 July 2018

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7 July 2018

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7 July 2018

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Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin-Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning

7 July 2018

1 reference

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7 July 2018

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7 July 2018

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A syndromic form of X-linked mental retardation: the Coffin-Lowry syndrome

7 July 2018

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7 July 2018

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7 July 2018

1 reference

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Cognitive impairment in Coffin-Lowry syndrome correlates with reduced RSK2 activation

7 July 2018

1 reference

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New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome

7 July 2018

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7 July 2018

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26 October 2018

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Expression of the RSK2 gene during early human development

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055244

Genetics of childhood disorders: LI. Learning and memory, Part 4: Human cognitive disorders and the ras/ERK/CREB pathway.

26 October 2018

1 reference

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Postmortem findings in the Coffin-Lowry Syndrome.

26 October 2018

1 reference

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Cognitive function in Coffin-Lowry syndrome

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055244

Brain-derived neurotrophic factor induces long-term potentiation in intact adult hippocampus: requirement for ERK activation coupled to CREB and upregulation of Arc synthesis.

26 October 2018

1 reference

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26 October 2018

1 reference

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26 October 2018

1 reference

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Reliability and validity of an algorithm for fuzzy tissue segmentation of MRI.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055244

26 October 2018

Coffin-Lowry syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17318637

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Changes in trkB-ERK1/2-CREB/Elk-1 pathways in hippocampal mossy fiber organization after traumatic brain injury

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17318637

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Callosal dysgenesis in a patient with Coffin-Lowry syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17318637

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10048-007-0080-6

1 reference

3 August 2017

1 reference

3 August 2017

1 reference