(Q48231304)

English

Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends

scientific article published in September 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

Nadia Chuzhanova

1

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

David N. Cooper

4

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

Michael Krawczak

3

object named as

Michael Krawczak

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

author name string

Shaun S Abeysinghe

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

publication date

1 September 2003

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

22

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

3

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

245-251

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs

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Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

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Palindrome resolution and recombination in the mammalian germ line

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Homologous recombination as a mechanism for genome rearrangements: environmental and genetic effects

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The role of DNA repeats and associated secondary structures in genomic instability and neoplasia

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Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexity

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A common molecular basis for rearrangement disorders on chromosome 22q11

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

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Double-strand breaks and translocations in cancer

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On the complexity measures of genetic sequences.

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The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors

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Sequence analysis of deletion mutations at the HPRT locus of human T-lymphocytes: association of a palindromic structure with a breakpoint cluster in exon 2

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Chromosomal translocations in human cancer.

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Coupled homologous and nonhomologous repair of a double-strand break preserves genomic integrity in mammalian cells

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Molecular analysis of bcl-1/IgH junctional sequences in mantle cell lymphoma: potential mechanism of the t(11;14) chromosomal translocation

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Genome architecture, rearrangements and genomic disorders

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The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers

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Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer.

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Chromosomal stability and the DNA double-stranded break connection

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Chromosome translocation based on illegitimate recombination in human tumors

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Identifiers

10.1002/HUMU.10253

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/12938089

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