(Q36549559)

14 August 2017

Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy (English)

1 reference

facioscapulohumeral muscular dystrophy

14 August 2017

0 references

R Tupler

1

0 references

author name string

G Perini

series ordinal

2

1 reference

14 August 2017

M A Pellegrino

series ordinal

3

1 reference

14 August 2017

M R Green

series ordinal

4

1 reference

14 August 2017

language of work or name

English

0 references

publication date

1 October 1999

1 reference

Proceedings of the National Academy of Sciences of the United States of America

14 August 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

14 August 2017

96

1 reference

14 August 2017

22

1 reference

14 August 2017

12650-12654

1 reference

Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

A screen for genes induced in the suprachiasmatic nucleus by light

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Differential screening and suppression subtractive hybridization identified genes differentially expressed in an estrogen receptor-positive breast carcinoma cell line

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Cloning the differences between two complex genomes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Basic local alignment search tool

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

DNA sequencing with chain-terminating inhibitors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23032

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

28 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.22.12650

Spreading the silence: epigenetic transcriptional regulation during Drosophila development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.22.12650

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.22.12650

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.22.12650

HMG17 is a chromatin-specific transcriptional coactivator that increases the efficiency of transcription initiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.22.12650

Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.22.12650

Improved methodology for analysis and quantitation of proteins on one-dimensional silver-stained slab gels

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.22.12650

A method for identifying differentially expressed genes in rare populations of primary human hematopoietic cells

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10535977

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.96.22.12650

1 reference

14 August 2017

0 references

1 reference

14 August 2017

1 reference