Non-B DNA conformations, genomic rearrangements, and human disease (Q35869768)

10 August 2017

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title

Non-B DNA conformations, genomic rearrangements, and human disease (English)

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10 August 2017

1

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10 August 2017

Robert D Wells

2

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PubMed ID

15326170

10 August 2017

language of work or name

English

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publication date

23 August 2004

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Journal of Biological Chemistry

10 August 2017

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10 August 2017

279

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10 August 2017

47411-47414

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10 August 2017

46

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The Role of DNA Structure in Genetic Regulatio

10 August 2017

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https://api.crossref.org/works/10.1074%2FJBC.R400028200

The structure of telomeric DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Identifying hydrogen bond alignments in multistranded DNA architectures by NMR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Definitions and analysis of DNA Holliday junction geometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Do natural DNA triple-helical structures occur and function in vivo?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Unusual DNA duplex and hairpin motifs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Dimeric DNA quadruplex containing major groove-aligned A-T-A-T and G-C-G-C tetrads stabilized by inter-subunit Watson-Crick A-T and G-C pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Double-strand breaks and translocations in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Breakpoints of gross deletions coincide with non-B DNA conformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

AT-rich palindromes mediate the constitutional t(11;22) translocation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Frequent chromosomal translocations induced by DNA double-strand breaks

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Molecular mechanisms for constitutional chromosomal rearrangements in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Abundant gene conversion between arms of palindromes in human and ape Y chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Genome architecture catalyzes nonrecurrent chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

The contribution of <i>cis</i>-elements to disease-associated repeat instability: clinical and experimental evidence

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Molecular basis of genetic instability of triplet repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Flexible DNA: genetically unstable CTG.CAG and CGG.CCG from human hereditary neuromuscular disease genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Molecular mechanism of class switch recombination: linkage with somatic hypermutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Transcription-targeted DNA deamination by the AID antibody diversification enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

R-loops at immunoglobulin class switch regions in the chromosomes of stimulated B cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Palindromic but not G-rich sequences are targets of class switch recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

AID enzyme-induced hypermutation in an actively transcribed gene in fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Mechanisms by which transcription can regulate somatic hypermutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

DNA inverted repeats and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Mutational mechanisms of Williams-Beuren syndrome deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R400028200

21 January 2018

Identifiers

DOI

10.1074/JBC.R400028200

1 reference

10 August 2017

1 reference

PubMed ID

15326170