(Q39369265)

English

Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats

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scholarly article

1 reference

Europe PubMed Central

11 September 2017

Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats (English)

1 reference

Europe PubMed Central

11 September 2017

author name string

Lena M Brueckner

1

1 reference

Europe PubMed Central

11 September 2017

Evgeny Sagulenko

2

1 reference

Europe PubMed Central

11 September 2017

Elisa M Hess

3

1 reference

Europe PubMed Central

11 September 2017

Diana Zheglo

4

1 reference

Europe PubMed Central

11 September 2017

Anne Blumrich

5

1 reference

Europe PubMed Central

11 September 2017

Manfred Schwab

6

1 reference

Europe PubMed Central

11 September 2017

Larissa Savelyeva

7

1 reference

Europe PubMed Central

11 September 2017

publication date

5 April 2012

1 reference

Europe PubMed Central

11 September 2017

1 reference

Europe PubMed Central

11 September 2017

131

1 reference

Europe PubMed Central

11 September 2017

1345-1359

1 reference

Europe PubMed Central

11 September 2017

8

1 reference

Europe PubMed Central

11 September 2017

https://scigraph.springernature.com/pub.10.1007/s00439-012-1165-3

0 references

Cycles of chromosome instability are associated with a fragile site and are increased by defects in DNA replication and checkpoint controls in yeast

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Inhibition of topoisomerase I prevents chromosome breakage at common fragile sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Common fragile sites as targets for chromosome rearrangements

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Comparison of constitutional and replication stress-induced genome structural variation by SNP array and mate-pair sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Signatures of mutation and selection in the cancer genome

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

The FRA2C common fragile site maps to the borders of MYCN amplicons in neuroblastoma and is associated with gross chromosomal rearrangements in different cancers.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

A-kinase anchoring protein 4 binding proteins in the fibrous sheath of the sperm flagellum

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Cytogenetics and DNA amplification in colorectal cancers

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Secondary structure formation and DNA instability at fragile site FRA16B

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

ATR Regulates Fragile Site Stability

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Functional and clinical significance of variants localized to 8q24 in colon cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Common fragile sites nested at the interfaces of early and late-replicating chromosome bands: cis acting components of the G2/M checkpoint?

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Common fragile sites: mechanisms of instability revisited.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

How common are common fragile sites in humans: interindividual variation in the distribution of aphidicolin-induced fragile sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

DNA instability at chromosomal fragile sites in cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Chromosome fragile sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Replication stress induces tumor-like microdeletions in FHIT/FRA3B

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinoma.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

DNA breaks at fragile sites generate oncogenic RET/PTC rearrangements in human thyroid cells

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

The functional role of long non-coding RNA in human carcinomas

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Common fragile sites.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Mechanisms for human genomic rearrangements

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

lincRNAs act in the circuitry controlling pluripotency and differentiation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

An oncogene-induced DNA damage model for cancer development

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C1--relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Sequence of the FRA3B common fragile region: implications for the mechanism of FHIT deletion

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Common fragile sites are characterized by histone hypoacetylation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Replication fork barriers: pausing for a break or stalling for time?

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Deletion at fragile sites is a common and early event in Barrett's esophagus.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Chromosomal translocations in yeast induced by low levels of DNA polymerase a model for chromosome fragile sites.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Failure of origin activation in response to fork stalling leads to chromosomal instability at fragile sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Breakages at common fragile sites set boundaries of amplified regions in two leukemia cell lines K562 - Molecular characterization of FRA2H and localization of a new CFS FRA2S.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Stably transfected common fragile site sequences exhibit instability at ectopic sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

The neurobeachin gene spans the common fragile site FRA13A.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

The molecular basis of common and rare fragile sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Interspersed repeats and other mementos of transposable elements in mammalian genomes

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Large common fragile site genes and cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Rare fragile sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Systematic identification of fragile sites via genome-wide location analysis of gamma-H2AX.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Oncogene-induced replication stress preferentially targets common fragile sites in preneoplastic lesions. A genome-wide study

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

An AT-rich sequence in human common fragile site FRA16D causes fork stalling and chromosome breakage in S. cerevisiae

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Molecular basis for expression of common and rare fragile sites

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1165-3

21 January 2018

Custom fluorescent-nucleotide synthesis as an alternative method for nucleic acid labeling

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the human common fragile site FRA2G

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal fragile site FRA16D and DNA instability in cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FRA1E common fragile site breaks map within a 370kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathology and biology associated with the fragile FHIT gene and gene product

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WWOX, the tumour suppressor gene affected in multiple cancers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role for common fragile site induction in amplification of human oncogenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel aphidicolin-inducible common fragile site FRA9G maps to 9p22.2, within the C9orf39 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/22476624

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-012-1165-3

1 reference

Europe PubMed Central

11 September 2017

1 reference

Europe PubMed Central

11 September 2017

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