(Q36059676)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

Design of an improved set of oligonucleotide primers for genotyping MeCP2tm1.1Bird KO mice by PCR (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

author name string

Julie Miralvès

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Eddy Magdeleine

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

publication date

31 August 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

Molecular Neurodegeneration

4 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

volume

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

page(s)

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

Repbase Update, a database of eukaryotic repetitive elements

4 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2018688

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2018688

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2018688

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2018688

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2018688

Male development of chromosomally female mice transgenic for Sry.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2018688

Breeding and maintenance of an Mecp2-deficient mouse model of Rett syndrome

11 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17764542

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1750-1326-2-16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

4 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764542%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

PubMed publication ID

17764542

1 reference