The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans (Q35704490)

9 August 2017

The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans (English)

1 reference

9 August 2017

Anne M Connolly

3

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Feng Zhang

object named as

Feng Zhang

1

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James R. Lupski

6

object named as

James R Lupski

1 reference

9 August 2017

Mehrdad Khajavi

2

1 reference

9 August 2017

Charles F Towne

4

1 reference

9 August 2017

Sat Dev Batish

5

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9 August 2017

language of work or name

English

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publication date

21 June 2009

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9 August 2017

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9 August 2017

41

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9 August 2017

849-853

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9 August 2017

7

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https://scigraph.springernature.com/pub.10.1038/ng.399

9 August 2017

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cites work

Complex human chromosomal and genomic rearrangements

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Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching

12 July 2018

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Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants

12 July 2018

1 reference

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A microhomology-mediated break-induced replication model for the origin of human copy number variation

12 July 2018

1 reference

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Increased LIS1 expression affects human and mouse brain development

12 July 2018

1 reference

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Mechanisms for human genomic rearrangements

12 July 2018

1 reference

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Segmental duplications arise from Pol32-dependent repair of broken forks through two alternative replication-based mechanisms

12 July 2018

1 reference

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Mapping and sequencing of structural variation from eight human genomes

12 July 2018

1 reference

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The fine-scale and complex architecture of human copy-number variation

12 July 2018

1 reference

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A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

12 July 2018

1 reference

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The mechanism of human nonhomologous DNA end joining

12 July 2018

1 reference

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

12 July 2018

1 reference

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Recurrent DNA inversion rearrangements in the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

12 July 2018

1 reference

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Global variation in copy number in the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Live-cell imaging reveals replication of individual replicons in eukaryotic replication factories

12 July 2018

1 reference

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Human genomic deletions mediated by recombination between Alu elements.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Structural variation in the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Fine-scale structural variation of the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Detection of large-scale variation in the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Large-scale copy number polymorphism in the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

An Alu Transposition Model for the Origin and Expansion of Human Segmental Duplications

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Genome architecture, rearrangements and genomic disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

12 July 2018

Evolution of novel genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Exon shuffling mimicked in cell culture

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Template switching during break-induced replication

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4461229

Complex gene rearrangements caused by serial replication slippage

25 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.399

The clinical spectrum associated with a chromosome 17 short arm proximal duplication (dup 17p11.2) in three patients

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.399

21 January 2018

Identifiers

DOI

10.1038/NG.399

1 reference

Dimensions Publication ID

9 August 2017

0 references

1 reference

9 August 2017

1 reference