(Q48008172)

English

Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene.

scientific article published in November 1998

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6 December 2019

Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene (English)

1 reference

Europe PubMed Central

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6 December 2019

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6 December 2019

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J C McNaughton

1

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6 December 2019

D J Cockburn

2

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6 December 2019

G Hughes

3

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6 December 2019

W A Jones

4

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6 December 2019

P N Ray

6

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6 December 2019

P A Stockwell

7

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6 December 2019

G B Petersen

8

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6 December 2019

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publication date

1 November 1998

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6 December 2019

1 reference

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6 December 2019

222

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6 December 2019

1

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6 December 2019

41-51

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6 December 2019

Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene

1 reference

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Nucleotide sequence preference at rat liver and wheat germ type 1 DNA topoisomerase breakage sites in duplex SV40 DNA

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7 January 2021

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242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

1 reference

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Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.

1 reference

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Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.

1 reference

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7 January 2021

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Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels

1 reference

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7 January 2021

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Analysis of a dystrophin gene deletion by amplification of mRNA isolated from DMD myotubes cultured in vitro

1 reference

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7 January 2021

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Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

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7 January 2021

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Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing

1 reference

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7 January 2021

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CENSOR--a program for identification and elimination of repetitive elements from DNA sequences

1 reference

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7 January 2021

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

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7 January 2021

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The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1 reference

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7 January 2021

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Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1 reference

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7 January 2021

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The human minisatellite consensus at breakpoints of oncogene translocations

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7 January 2021

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Sequences of junction fragments in the deletion-prone region of the dystrophin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900466-1

7 January 2021

based on heuristic

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A cluster of transposon-like repetitive sequences in intron 7 of the human dystrophin gene

1 reference

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7 January 2021

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The evolution of an intron: analysis of a long, deletion-prone intron in the human dystrophin gene

1 reference

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7 January 2021

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Exon–Intron Organization of the Human Dystrophin Gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900466-1

7 January 2021

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Two hot spots of recombination in the DMD gene correlate with the deletion prone regions

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900466-1

7 January 2021

based on heuristic

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A transposon-like element in the deletion-prone region of the dystrophin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900466-1

7 January 2021

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A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

1 reference

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7 January 2021

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A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesis.

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7 January 2021

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Drosophila topoisomerase II double-strand DNA cleavage: analysis of DNA sequence homology at the cleavage site

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A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

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Dysfunction of chromosomal loop attachment sites: illegitimate recombination linked to matrix association regions and topoisomerase II.

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A consensus sequence for cleavage by vertebrate DNA topoisomerase II.

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7 January 2021

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Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis

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Identifiers

10.1016/S0378-1119(98)00466-1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9813236%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9813236%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

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