(Q71468182)

English

Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat family

scientific article published on 01 September 1996

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8781186%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat family (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8781186%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

author name string

L N Clark

1

1 reference

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18 October 2019

U Koehler

2

1 reference

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18 October 2019

D C Ward

3

1 reference

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18 October 2019

J Wienberg

4

1 reference

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18 October 2019

J E Hewitt

5

1 reference

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18 October 2019

publication date

1 September 1996

1 reference

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18 October 2019

1 reference

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18 October 2019

105

1 reference

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18 October 2019

180-189

1 reference

Europe PubMed Central

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18 October 2019

3

1 reference

Europe PubMed Central

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18 October 2019

https://scigraph.springernature.com/pub.10.1007/bf02509499

0 references

Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

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/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of GC-rich repetitive nucleotide sequences in great apes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA DIVERGENCE AMONG HOMINOIDS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of the chAB4 multisequence family in primates.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy familes (FSHD) with 4q markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: implications for recombination between nonhomologues and Robertsonian translocations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

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/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

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/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of human extrachromosomal DNA elements originating from different beta-satellite subfamilies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA hybridization evidence of hominoid phylogeny: a reanalysis of the data

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mammalian chromosome structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

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/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

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/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reconstruction of genomic rearrangements in great apes and gibbons by chromosome painting

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

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/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypermethylation of human DNA sequences in embryonal carcinoma cells and somatic tissues but not in sperm

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 724 family of DNA sequences is interspersed about the pericentromeric regions of human acrocentric chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative high-resolution mapping of human and primate chromosomes by fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8781186

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02509499

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8781186%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8781186%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

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