(Q36512738)

14 August 2017

Modeling Rett syndrome with stem cells (English)

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14 August 2017

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2

Konrad Hochedlinger

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author name string

Ryan M Walsh

series ordinal

1

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14 August 2017

language of work or name

English

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publication date

1 November 2010

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14 August 2017

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14 August 2017

143

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14 August 2017

4

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14 August 2017

499-500

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A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

Induced pluripotency: history, mechanisms, and applications

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

Female human iPSCs retain an inactive X chromosome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

Reversal of neurological defects in a mouse model of Rett syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

Rett syndrome: model of neurodevelopmental disorders

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3538362

10.1016/J.CELL.2010.10.037

30 September 2017

Identifiers

DOI

1 reference

release_l44esuljyzbslhsongjanmsq5i

14 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/l44esuljyzbslhsongjanmsq5i

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

14 August 2017

PubMed publication ID

21074040

1 reference