(Q36684143)

15 August 2017

DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex (English)

1 reference

15 August 2017

Masaru Miyano

1

1 reference

15 August 2017

Shin-ichi Horike

2

1 reference

15 August 2017

Shutao Cai

3

1 reference

15 August 2017

Mitsuo Oshimura

4

1 reference

15 August 2017

Terumi Kohwi-Shigematsu

5

1 reference

15 August 2017

5 June 2008

1 reference

Journal of Cellular and Molecular Medicine

15 August 2017

1 reference

15 August 2017

12

1 reference

15 August 2017

4

1 reference

15 August 2017

1188-1191

1 reference

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

Loss of silent-chromatin looping and impaired imprinting of DLX5 in 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=3597349

A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

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=3597349

A highly conserved enhancer in the Dlx5/Dlx6 intergenic region is the site of cross-regulatory interactions between Dlx genes in the embryonic forebrain.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3597349

Dlx5, the mouse homologue of the human-imprinted DLX5 gene, is biallelically expressed in the mouse brain.

30 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1582-4934.2008.00377.X

10.1111/J.1582-4934.2008.00377.X

21 January 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

18537997

1 reference