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Large transcription units unify copy number variants and common fragile sites arising under replication stress

Genome research, 2015-02, Vol.25 (2), p.189-200

2015

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De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining

PLoS genetics, 2012-09, Vol.8 (9), p.e1002981

2012

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Replication stress and mechanisms of CNV formation

Current opinion in genetics & development, 2012-06, Vol.22 (3), p.204-210

2012

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Fragile sites in cancer: more than meets the eye

Nature reviews. Cancer, 2017-08, Vol.17 (8), p.489-501

2017

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ATR Regulates Fragile Site Stability

Cell, 2002-12, Vol.111 (6), p.779-789

2002

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Establishing the Usability of a Virtual Training System for Assembly Operations within the Automotive Industry

Human factors and ergonomics in manufacturing & service industries, 2016-11, Vol.26 (6), p.667-679

2016

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Hydroxyurea induces de novo copy number variants in human cells

Proceedings of the National Academy of Sciences - PNAS, 2011-10, Vol.108 (42), p.17360-17365

2011

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Mutations in FOXC2 ( MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

American journal of human genetics, 2000-12, Vol.67 (6), p.1382-1388

2000

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Common fragile sites as targets for chromosome rearrangements

DNA repair, 2006-09, Vol.5 (9), p.1126-1135

2006

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Mechanisms of common fragile site instability

Human molecular genetics, 2005-10, Vol.14 (suppl-2), p.R197-R205

2005

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Quality of life in patients with unilateral vestibular schwannoma on wait and see - strategy

Neurological research (New York), 2018-01, Vol.40 (1), p.34-40

2018

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Replication stress induces tumor-like microdeletions in FHIT/FRA3B

Proceedings of the National Academy of Sciences - PNAS, 2008-01, Vol.105 (1), p.246-251

2008

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Using δ13C of Levoglucosan As a Chemical Clock

Environmental science & technology, 2018-10, Vol.52 (19), p.11094-11101

2018

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Genomic Structure, Evolutionary Origins, and Reproductive Function of a Large Amplified Intrinsically Disordered Protein-Coding Gene on the X Chromosome ( Laidx ) in Mice

G3 : genes - genomes - genetics, 2020-06, Vol.10 (6), p.1997-2005

2020

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Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites

Oncogene, 2006-07, Vol.25 (32), p.4381-4388

2006

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High Resolution Imaging of Viscoelastic Properties of Intracranial Tumours by Multi-Frequency Magnetic Resonance Elastography

Clinical neuroradiology (Munich), 2015-12, Vol.25 (4), p.371-378

2015

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Chromosomal Instability at Common Fragile Sites in Seckel Syndrome

American journal of human genetics, 2004-10, Vol.75 (4), p.654-660

2004

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BRCA1 Is Required for Common-Fragile-Site Stability via Its G2/M Checkpoint Function

Molecular and Cellular Biology, 2004-08, Vol.24 (15), p.6701-6709

2004

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Cerebrospinal fluid leak after microsurgical surgery in vestibular schwannomas via retrosigmoidal craniotomy

Neurological research (New York), 2011-11, Vol.33 (9), p.947-952

2011

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Locus-specific transcription silencing at the FHIT gene suppresses replication stress-induced copy number variant formation and associated replication delay

Nucleic acids research, 2021-07, Vol.49 (13), p.7507-7524

2021

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

Genetics (Austin), 2011-03, Vol.187 (3), p.675-683

2011

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

Genes chromosomes & cancer, 2002-01, Vol.33 (1), p.82-92

2002

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Recurrence rate, time to progression and facial nerve function in microsurgery of vestibular schwannoma

Neurological research (New York), 2011-12, Vol.33 (10), p.1032-1037

2011

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A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome

Journal of medical genetics, 2017-03, Vol.54 (3), p.212-216

2017

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Common fragile sites

Cytogenetic and Genome Research, 2003-01, Vol.100 (1-4), p.92-100

2003

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Large transcription units unify copy number variants and common fragile sites arising under replication stress

De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining

Replication stress and mechanisms of CNV formation

Fragile sites in cancer: more than meets the eye

ATR Regulates Fragile Site Stability

Establishing the Usability of a Virtual Training System for Assembly Operations within the Automotive Industry

Hydroxyurea induces de novo copy number variants in human cells

Mutations in FOXC2 ( MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Common fragile sites as targets for chromosome rearrangements

Mechanisms of common fragile site instability

Quality of life in patients with unilateral vestibular schwannoma on wait and see - strategy

Replication stress induces tumor-like microdeletions in FHIT/FRA3B

Using δ13C of Levoglucosan As a Chemical Clock

Genomic Structure, Evolutionary Origins, and Reproductive Function of a Large Amplified Intrinsically Disordered Protein-Coding Gene on the X Chromosome ( Laidx ) in Mice

Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites

High Resolution Imaging of Viscoelastic Properties of Intracranial Tumours by Multi-Frequency Magnetic Resonance Elastography

Chromosomal Instability at Common Fragile Sites in Seckel Syndrome

BRCA1 Is Required for Common-Fragile-Site Stability via Its G2/M Checkpoint Function

Cerebrospinal fluid leak after microsurgical surgery in vestibular schwannomas via retrosigmoidal craniotomy

Locus-specific transcription silencing at the FHIT gene suppresses replication stress-induced copy number variant formation and associated replication delay

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

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

Recurrence rate, time to progression and facial nerve function in microsurgery of vestibular schwannoma

A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome

Common fragile sites

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