(Q46971971)

English

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.

scientific article published in May 1994

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scholarly article

1 reference

Europe PubMed Central

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24 October 2019

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 (English)

1 reference

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24 October 2019

facioscapulohumeral muscular dystrophy

0 references

Katherine Mathews

4

1 reference

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24 October 2019

author name string

S T Winokur

1

1 reference

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24 October 2019

U Bengtsson

2

1 reference

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24 October 2019

J Feddersen

3

1 reference

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24 October 2019

B Weiffenbach

5

1 reference

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24 October 2019

H Bailey

6

1 reference

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24 October 2019

R P Markovich

7

1 reference

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24 October 2019

J C Murray

8

1 reference

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24 October 2019

J J Wasmuth

9

1 reference

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24 October 2019

M R Altherr

10

1 reference

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24 October 2019

publication date

1 May 1994

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24 October 2019

Chromosome Research

1 reference

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24 October 2019

2

1 reference

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24 October 2019

3

1 reference

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24 October 2019

225-234

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24 October 2019

https://scigraph.springernature.com/pub.10.1007/bf01553323

0 references

Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the committee on the genetic constitution of chromosome 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counselling in facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modifiers of position effect are shared between telomeric and silent mating-type loci in S. cerevisiae.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal position and activation of retroviral genomes inserted into the germ line of mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transformation of white locus DNA in drosophila: dosage compensation, zeste interaction, and position effects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Position-effect variegation--an assay for nonhistone chromosomal proteins and chromatin assembly and modifying factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterochromatin and satellite DNA in man: properties and prospects

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effects of chromosome rearrangements on the expression of heterochromatic genes in chromosome 2L of Drosophila melanogaster

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structure of a subterminal repeated sequence present on many human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Position effect variegation in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly repeated sequences in mammalian genomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Location of Ribosomal DNA in the Human Chromosome Complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of a foreign gene in a line of transgenic mice is modulated by a chromosomal position effect

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomere-proximal DNA in Saccharomyces cerevisiae is refractory to methyltransferase activity in vivo

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome banding in amphibia. XI. Constitutive heterochromatin, nucleolus organizers, 18S + 28S and 5S ribosomal RNA genes in Ascaphidae, Pipidae, Discoglossidae and Pelobatidae

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of heterochromatin in the expression of a heterochromatic gene, the rolled locus of Drosophila melanogaster

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimating genomic distance from DNA sequence location in cell nuclei by a random walk model

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence definition and organization of a human repeated DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counterselective procedure to isolate interspecific cell hybrids containing single human chromosomes: construction of cell hybrids and recombinant DNA libraries specific for human chromosomes 3 and 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Position effect variegation in Drosophila: towards a genetics of chromatin assembly

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution patterns of HP1, a heterochromatin-associated nonhistone chromosomal protein of Drosophila

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A structural basis for variegating position effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome bands, their chromatin flavors, and their functional features

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sixty years of mystery

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visualization of nucleolar organizer regions in mammalian chromosomes using silver staining

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Position-effect variegation after 60 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Basic local alignment search tool

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular organization and chromosomal location of human GC-rich heterochromatic blocks.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage in human heterochromatin between highly divergent Sau3A repeats and a new family of repeated DNA sequences (HaeIII family).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive set of sequence analysis programs for the VAX

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The proximity of DNA sequences in interphase cell nuclei is correlated to genomic distance and permits ordering of cosmids spanning 250 kilobase pairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of He-T DNA sequences in the pericentric regions of Drosophila chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution mapping of mammalian genes by in situ hybridization to free chromatin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved sequencing of cosmids using new primers and linearized DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Position effect at S. cerevisiae telomeres: reversible repression of Pol II transcription

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal location by in situ hybridization of the human Sau3A family of DNA repeats

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Untwirling dirvish

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine mapping of human 5S rRNA genes to chromosome 1q42.11→q42.13

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic criteria for facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region

1 reference

https://pubmed.ncbi.nlm.nih.gov/8069466

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01553323

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8069466%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8069466%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

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