Mattias Höglund
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- 2005
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Mark
Telomere-mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma
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- Contribution to journal › Article
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Mark
Statistical behavior of complex cancer karyotypes.
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- Contribution to journal › Scientific review
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Mark
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.
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- Contribution to journal › Article
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Mark
Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer.
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- Contribution to journal › Article
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Mark
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
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- Contribution to journal › Article
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Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
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- Contribution to journal › Article
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Mark
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
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- Contribution to journal › Article
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Mark
Connecting mitotic instability and chromosome aberrations in cancer-can telomeres bridge the gap?
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- Contribution to journal › Scientific review
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Mark
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations
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- Contribution to journal › Article
- 2004
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Mark
A model for karyotypic evolution in testicular germ cell tumors.
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- Contribution to journal › Article
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Mark
Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.
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- Contribution to journal › Article
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Mark
Approximate geodesic distances reveal biologically relevant structures in microarray data
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- Contribution to journal › Article
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Mark
Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution.
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- Contribution to journal › Article
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Mark
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
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- Contribution to journal › Article
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Mark
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
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- Contribution to journal › Article