(Q38042854)

27 August 2017

Chromothripsis and cancer: causes and consequences of chromosome shattering (English)

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27 August 2017

2

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27 August 2017

3

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27 August 2017

Josep V Forment

1

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language of work or name

English

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publication date

13 September 2012

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27 August 2017

Nature Reviews Cancer

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27 August 2017

12

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27 August 2017

663-670

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27 August 2017

10

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https://scigraph.springernature.com/pub.10.1038/nrc3352

27 August 2017

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cites work

Hallmarks of Cancer: The Next Generation

1 reference

The impact of translocations and gene fusions on cancer causation

31 March 2020

1 reference

Massive genomic rearrangement acquired in a single catastrophic event during cancer development

31 March 2020

1 reference

DNA double-strand break repair pathways, chromosomal rearrangements and cancer

31 March 2020

1 reference

Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications

31 March 2020

1 reference

The DNA Damage Response: Making It Safe to Play with Knives

31 March 2020

1 reference

Pathways of mammalian replication fork restart.

31 March 2020

1 reference

Preventing nonhomologous end joining suppresses DNA repair defects of Fanconi anemia.

31 March 2020

1 reference

Ku70 corrupts DNA repair in the absence of the Fanconi anemia pathway

31 March 2020

1 reference

The DNA-damage response in human biology and disease

31 March 2020

1 reference

An oncogene-induced DNA damage model for cancer development

31 March 2020

1 reference

Mechanisms for recurrent and complex human genomic rearrangements

31 March 2020

1 reference

Complex human chromosomal and genomic rearrangements

31 March 2020

1 reference

Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer

31 March 2020

1 reference

Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients

31 March 2020

1 reference

Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes

31 March 2020

1 reference

Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms

31 March 2020

1 reference

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

31 March 2020

1 reference

Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements

31 March 2020

1 reference

Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†

31 March 2020

1 reference

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

31 March 2020

1 reference

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

31 March 2020

1 reference

Chromothripsis and human disease: piecing together the shattering process.

31 March 2020

1 reference

When catastrophe strikes a cell

31 March 2020

1 reference

The consequences of structural genomic alterations in humans: genomic disorders, genomic instability and cancer

31 March 2020

1 reference

Cancer genomes evolve by pulverizing single chromosomes

31 March 2020

1 reference

DNA breaks and chromosome pulverization from errors in mitosis

31 March 2020

1 reference

DNA damage signaling in response to double-strand breaks during mitosis

31 March 2020

1 reference

A mitotic phosphorylation feedback network connects Cdk1, Plk1, 53BP1, and Chk2 to inactivate the G(2)/M DNA damage checkpoint

31 March 2020

1 reference

Mammalian Cell Fusion : Induction of Premature Chromosome Condensation in Interphase Nuclei

31 March 2020

1 reference

Lagging chromosomes entrapped in micronuclei are not 'lost' by cells

31 March 2020

1 reference

Spatial organization of the mouse genome and its role in recurrent chromosomal translocations

31 March 2020

1 reference

Molecular mechanisms of micronucleus, nucleoplasmic bridge and nuclear bud formation in mammalian and human cells

31 March 2020

1 reference

Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations

31 March 2020

1 reference

Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells

31 March 2020

1 reference

Whole chromosome instability caused by Bub1 insufficiency drives tumorigenesis through tumor suppressor gene loss of heterozygosity

31 March 2020

1 reference

Proliferation of aneuploid human cells is limited by a p53-dependent mechanism.

31 March 2020

1 reference

The ATM-p53 pathway suppresses aneuploidy-induced tumorigenesis

31 March 2020

1 reference

Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations

31 March 2020

1 reference

Functional genomic screens identify CINP as a genome maintenance protein

31 March 2020

1 reference

Evidence for chromosome instability in vivo in bloom syndrome: Increased numbers of micronuclei in exfoliated cells

31 March 2020

1 reference

The DNA damage response and cancer therapy

31 March 2020

1 reference

Mutational processes molding the genomes of 21 breast cancers

31 March 2020

1 reference

Template Switching: From Replication Fork Repair to Genome Rearrangements

31 March 2020

1 reference

Merotelic kinetochore orientation, aneuploidy, and cancer.

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22972457

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sensitivity to five mutagens in Fanconi's anemia as measured by the micronucleus method

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22972457

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRC3352

1 reference

PubMed ID

22972457

Dimensions Publication ID

27 August 2017

1026374177

0 references

Fatcat ID

release_wfkua66vzbdtjk2axcipb6lvsi

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wfkua66vzbdtjk2axcipb6lvsi

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

22972457

1 reference

PubMed ID

22972457