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- Publications
- Influence
High-resolution analysis of DNA copy number using oligonucleotide microarrays.
- G. Bignell, Jing Huang, +11 authors R. Wooster
- Biology, Medicine
- Genome research
- 1 February 2004
Genomic copy number alterations are a feature of many human diseases including cancer. We have evaluated the effectiveness of an oligonucleotide array, originally designed to detect single-nucleotide… Expand
Recent developments in the assessment of chromosomal damage.
- A. T. Natarajan, A. Balajee, +7 authors S. Vermeulen
- Biology, Medicine
- International journal of radiation biology
- 1994
Ionizing radiation and restriction endonucleases are very efficient in inducing chromosomal aberrations (CAs). These aberrations are mainly consequences of misrepair of DNA double-strand breaks… Expand
Cytogenetic effects of hexavalent chromium in Bulgarian chromium platers.
- D. Benova, V. Hadjidekova, +10 authors R. Nilsson
- Biology, Medicine
- Mutation research
- 15 February 2002
The aim of the present study was to evaluate the genotoxic effects of hexavalent chromium (Cr(VI)) in vivo in exposed Bulgarian chromium platers by using classical cytogenetic and molecular… Expand
Haplotype Structure of FSHB, the Beta-Subunit Gene for Fertility-Associated Follicle-Stimulating Hormone: Possible Influence of Balancing Selection
- M. Grigorova, K. Rull, M. Laan
- Biology, Medicine
- Annals of human genetics
- 1 January 2007
Follicle‐stimulating hormone (FSH) is essential for human reproduction. The unique functions of this hormone are provided by the FSH receptor‐binding beta‐subunit encoded by the FSHB gene.… Expand
137Cesium-induced chromosome aberrations analyzed by fluorescence in situ hybridization: eight years follow up of the Goiânia radiation accident victims.
- A. T. Natarajan, S. J. Santos, +9 authors M. Curado
- Biology, Medicine
- Mutation research
- 25 May 1998
The radiation accident in focus here occurred in a section of Goiânia (Brazil) where more than a hundred individuals were contaminated with 137Cesium on September 1987. In order to estimate the… Expand
Induction and persistence of chromosomal exchanges in mouse bone marrow cells following whole-body exposure to X-rays.
- Y. Xiao, F. Darroudi, M. Grigorova, A. T. Natarajan
- Biology, Medicine
- International journal of radiation biology
- 1 September 1999
PURPOSE
To investigate the induction and persistence of chromosome aberrations in mouse bone marrow cells after X-ray exposure and to detect differential involvement of individual chromosomes in… Expand
Frequencies and types of exchange aberrations induced by X-rays and neutrons in Chinese hamster splenocytes detected by FISH using chromosome-specific DNA libraries.
- M. Grigorova, R. Brand, Y. Xiao, A. T. Natarajan
- Biology, Medicine
- International journal of radiation biology
- 1998
PURPOSE
To estimate the frequencies of radiation- (low and high LET) induced chromosome aberrations in Chinese hamster splenocytes by two-colour fluorescence in situ hybridization using DNA painting… Expand
Possible causes of chromosome instability: comparison of chromosomal abnormalities in cancer cell lines with mutations in BRCA1, BRCA2, CHK2 and BUB1
- M. Grigorova, J. M. Staines, H. Ozdag, C. Caldas, P. A. Edwards
- Biology, Medicine
- Cytogenetic and Genome Research
- 2004
A large proportion of epithelial cancers show the chromosome-instability phenotype, in which they have many chromosome abnormalities. This is thought to be the result of mutations that disrupt… Expand
Chromosome abnormalities in 10 lung cancer cell lines of the NCI-H series analyzed with spectral karyotyping.
- M. Grigorova, Rachel C Lyman, C. Caldas, P. Edwards
- Biology, Medicine
- Cancer genetics and cytogenetics
- 1 October 2005
The karyotypes of 10 lung cancer cell lines of the NCI-H series were analyzed with spectral karyotyping (SKY): 7 non-small lung cancer (NSCLC) lines and 3 small cell lung cancer (SCLC) lines. Modal… Expand
Single-cell sequencing of genomic DNA resolves sub-clonal heterogeneity in a melanoma cell line
- Enrique I. Velazquez-Villarreal, Shamoni Maheshwari, +9 authors D. Craig
- Biology, Medicine
- Communications Biology
- 25 June 2020
We performed shallow single-cell sequencing of genomic DNA across 1475 cells from a cell-line, COLO829, to resolve overall complexity and clonality. This melanoma tumor-line has been previously… Expand