4.6 Review

A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

Related references

Note: Only part of the references are listed.
Article Cell Biology

Break-induced replication - What is it and what is it for?

Bertrand Llorente et al.

CELL CYCLE (2008)

Article Biochemistry & Molecular Biology

Rad51 protein controls Rad52-mediated DNA annealing

Yun Wu et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2008)

Article Genetics & Heredity

Double complex mutations involving F8 and FUNDC2 caused by distinct break-induced replication

Campbell R. Sheen et al.

HUMAN MUTATION (2007)

Article Biochemistry & Molecular Biology

An evolution revolution provides further revelation

James R. Lupski

BIOESSAYS (2007)

Article Multidisciplinary Sciences

Paired-end mapping reveals extensive structural variation in the human genome

Jan O. Korbel et al.

SCIENCE (2007)

Article Multidisciplinary Sciences

Gene duplication and the adaptive evolution of a classic genetic switch

Chris Todd Hittinger et al.

NATURE (2007)

Article Multidisciplinary Sciences

Rag mutations reveal robust alternative end joining

Barbara Corneo et al.

NATURE (2007)

Article Biochemistry & Molecular Biology

Gene copy number variation spanning 60 million years of human and primate evolution

Laura Dumas et al.

GENOME RESEARCH (2007)

Article Biochemistry & Molecular Biology

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

Graham R. Bignell et al.

GENOME RESEARCH (2007)

Article Multidisciplinary Sciences

Break-induced replication and telomerase-independent telomere maintenance require Pol32

John R. Lydeard et al.

NATURE (2007)

Article Genetics & Heredity

Spontaneous DNA breakage in single living Escherichia coli cells

Jeanine M. Pennington et al.

NATURE GENETICS (2007)

Review Oncology

Regulation of DNA repair in hypoxic cancer cells

Ranjit S. Bindra et al.

CANCER AND METASTASIS REVIEWS (2007)

Article Multidisciplinary Sciences

Template switching during break-induced replication

Catherine E. Smith et al.

NATURE (2007)

Article Biochemistry & Molecular Biology

Ability of polymerase η and T7 DNA polymerase to bypass bulge structures

Vincent J. Cannistraro et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2007)

Article Biochemistry & Molecular Biology

Inverted DNA repeats channel repair of distant double-strand breaks into chromatid fusions and chromosomal rearrangements

Kelly VanHulle et al.

MOLECULAR AND CELLULAR BIOLOGY (2007)

Article Biochemistry & Molecular Biology

Repression of RAD51 gene expression by E2F4/p130 complexes in hypoxia

R. S. Bindra et al.

ONCOGENE (2007)

Review Genetics & Heredity

Hypoxia-induced genetic instability - a calculated mechanism underlying tumor progression

L. Eric Huang et al.

JOURNAL OF MOLECULAR MEDICINE-JMM (2007)

Review Biochemistry & Molecular Biology

Adaptive amplification

P. J. Hastings

CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY (2007)

Article Genetics & Heredity

A comprehensive analysis of common copy-number variations in the human genome

Kendy K. Wong et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2007)

Article Biochemistry & Molecular Biology

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

Daisuke Komura et al.

GENOME RESEARCH (2006)

Article Genetics & Heredity

Genome assembly comparison identifies structural variants in the human genome

Razi Khaja et al.

NATURE GENETICS (2006)

Article Biochemistry & Molecular Biology

Accurate and reliable high-throughput detection of copy number variation in the human genome

Heike Fiegler et al.

GENOME RESEARCH (2006)

Article Multidisciplinary Sciences

Global variation in copy number in the human genome

Richard Redon et al.

NATURE (2006)

Article Multidisciplinary Sciences

Multiple pathways of selected gene amplification during adaptive mutation

Elisabeth Kugelberg et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Biochemistry & Molecular Biology

Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease

Jennifer A. Lee et al.

HUMAN MOLECULAR GENETICS (2006)

Review Biochemistry & Molecular Biology

Control of translocations between highly diverged genes by Sgs1, the Saccharomyces cerevisiae homolog of the Bloom's syndrome protein

Kristina H. Schmidt et al.

MOLECULAR AND CELLULAR BIOLOGY (2006)

Review Genetics & Heredity

Primate segmental duplications: crucibles of evolution, diversity and disease

Jeffrey A. Bailey et al.

NATURE REVIEWS GENETICS (2006)

Article Genetics & Heredity

On the mechanism of gene amplification induced under stress in Escherichia coli

Andrew Slack et al.

PLOS GENETICS (2006)

Article Biochemistry & Molecular Biology

Decoding the fine-scale structure of a breast cancer genome and transcriptome

S Volik et al.

GENOME RESEARCH (2006)

Article Biochemistry & Molecular Biology

Dual roles for DNA polymerase η in homologous DNA recombination and translesion DNA synthesis

T Kawamoto et al.

MOLECULAR CELL (2005)

Article Biochemistry & Molecular Biology

A genome-wide survey of structural variation between human and chimpanzee

TL Newman et al.

GENOME RESEARCH (2005)

Article Biochemistry & Molecular Biology

Spontaneous homologous recombination is induced by collapsed replication forks that are caused by endogenous DNA single-strand breaks

N Saleh-Gohari et al.

MOLECULAR AND CELLULAR BIOLOGY (2005)

Article Genetics & Heredity

Fine-scale structural variation of the human genome

E Tuzun et al.

NATURE GENETICS (2005)

Article Biochemistry & Molecular Biology

RAD51-dependent break-induced replication in yeast

AP Davis et al.

MOLECULAR AND CELLULAR BIOLOGY (2004)

Article Genetics & Heredity

Detection of large-scale variation in the human genome

AJ Iafrate et al.

NATURE GENETICS (2004)

Article Multidisciplinary Sciences

Large-scale copy number polymorphism in the human genome

J Sebat et al.

SCIENCE (2004)

Article Biochemistry & Molecular Biology

Serial segmental duplications during primate evolution result in complex human genome architecture

P Stankiewicz et al.

GENOME RESEARCH (2004)

Article Biochemistry & Molecular Biology

Down-regulation of Rad51 and decreased homologous recombination in hypoxic cancer cells

RS Bindra et al.

MOLECULAR AND CELLULAR BIOLOGY (2004)

Review Genetics & Heredity

Birth of 'human-specific' genes during primate evolution

JL Nahon

GENETICA (2003)

Article Genetics & Heredity

Genome architecture catalyzes nonrecurrent chromosomal rearrangements

P Stankiewicz et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2003)

Article Biochemistry & Molecular Biology

Decreased expression of the DNA mismatch repair gene Mlh1 under hypoxic stress in mammalian cells

VT Mihaylova et al.

MOLECULAR AND CELLULAR BIOLOGY (2003)

Review Oncology

The hypoxic tumour microenvironment and metastatic progression

P Subarsky et al.

CLINICAL & EXPERIMENTAL METASTASIS (2003)

Article Genetics & Heredity

Analysis of 22 deletion breakpoints in dystrophin intron 49

C Nobile et al.

HUMAN GENETICS (2002)

Article Multidisciplinary Sciences

Genomic DNA breakpoints in AML1/RUNX1 and ETO cluster with topoisomerase II DNA cleavage and DNase I hypersensitive sites in t(8;21) leukemia

YM Zhang et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)

Review Genetics & Heredity

Genome architecture, rearrangements and genomic disorders

P Stankiewicz et al.

TRENDS IN GENETICS (2002)

Article Multidisciplinary Sciences

Instability of repetitive DNA sequences: The role of replication in multiple mechanisms

M Bzymek et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)

Article Biochemistry & Molecular Biology

Adaptive amplification: An inducible chromosomal instability mechanism

PJ Hastings et al.