(Q34333357)

1 August 2017

title

Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination (English)

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1 August 2017

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2

Tomasz Gambin

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1 August 2017

8

Anna Gambin

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1 August 2017

Ian M Campbell

1

0 references

Pawel Stankiewicz

11

object named as

Paweł Stankiewicz

1 reference

1 August 2017

7

Ankita Patel

1 reference

1 August 2017

Piotr Dittwald

3

1 reference

1 August 2017

Christine R Beck

4

1 reference

1 August 2017

Andrey Shuvarikov

5

1 reference

1 August 2017

Patricia Hixson

6

1 reference

1 August 2017

Chad A Shaw

9

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1 August 2017

Jill A Rosenfeld

10

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1 August 2017

publication date

23 September 2014

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1 August 2017

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1 August 2017

volume

12

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1 August 2017

page(s)

74

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Creative Commons Attribution 4.0 International

1 August 2017

copyright license

start time

23 September 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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6 July 2018

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Mechanisms for recurrent and complex human genomic rearrangements

6 July 2018

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A recurrent translocation is mediated by homologous recombination between HERV-H elements

6 July 2018

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Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-over

6 July 2018

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LINE-1 elements in structural variation and disease

6 July 2018

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Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome

6 July 2018

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Structural variation in the human genome and its role in disease

6 July 2018

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PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice

6 July 2018

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6 July 2018

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Mechanisms for human genomic rearrangements

6 July 2018

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

6 July 2018

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Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

6 July 2018

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Genomic rearrangements and sporadic disease

6 July 2018

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The evolutionary dynamics of human endogenous retroviral families

6 July 2018

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Segmental duplications and copy-number variation in the human genome

6 July 2018

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HERVd: the Human Endogenous RetroViruses Database: update

6 July 2018

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The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats

6 July 2018

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Evidence for genomic rearrangements mediated by human endogenous retroviruses during primate evolution

6 July 2018

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6 July 2018

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6 July 2018

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LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis

6 July 2018

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Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients

6 July 2018

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Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease

6 July 2018

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A general method for the identification of transcribed retrovirus sequences (R-U5 PCR) reveals the expression of the human endogenous retrovirus loci HERV-H and HERV-K in teratocarcinoma cells

6 July 2018

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Dependence of intrachromosomal recombination in mammalian cells on uninterrupted homology

6 July 2018

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Long interspersed nuclear element-1 (LINE1)-mediated deletion of EVC, EVC2, C4orf6, and STK32B in Ellis-van Creveld syndrome with borderline intelligence.

6 July 2018

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New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome.

21 January 2018

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HERV-mediated genomic rearrangement of EYA1 in an individual with branchio-oto-renal syndrome

21 January 2018

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Definition and variation of human endogenous retrovirus H.

21 January 2018

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A common sequence motif associated with recombination hot spots and genome instability in humans

21 January 2018

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21 January 2018

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Development and validation of a CGH microarray for clinical cytogenetic diagnosis

21 January 2018

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Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25246103

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25246103

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25246103

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12915-014-0074-4

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference

1 August 2017

1 reference