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  1. No Access

    Protocol

    Profiling Numerical and Structural Chromosomal Instability in Different Cancer Types

    Many cancers display whole chromosome instability (W-CIN) and structural chromosomal instability (S-CIN), referring to increased rates of acquiring numerically and structurally abnormal chromosome changes. Thi...

    **aoxiao Zhang, Maik Kschischo in Cancer Cytogenetics and Cytogenomics (2024)

  2. Article

    Open Access

    Generation of realistic synthetic data using Multimodal Neural Ordinary Differential Equations

    Individual organizations, such as hospitals, pharmaceutical companies, and health insurance providers, are currently limited in their ability to collect data that are fully representative of a disease populati...

    Philipp Wendland, Colin Birkenbihl, Marc Gomez-Freixa in npj Digital Medicine (2022)

  3. Article

    Open Access

    Loss of USP28 and SPINT2 expression promotes cancer cell survival after whole genome doubling

    Whole genome doubling is a frequent event during cancer evolution and shapes the cancer genome due to the occurrence of chromosomal instability. Yet, erroneously arising human tetraploid cells usually do not p...

    Sara Vanessa Bernhard, Katarzyna Seget-Trzensiok, Christian Kuffer in Cellular Oncology (2022)

  4. Article

    Open Access

    Systems approaches identify the consequences of monosomy in somatic human cells

    Chromosome loss that results in monosomy is detrimental to viability, yet it is frequently observed in cancers. How cancers survive with monosomy is unknown. Using p53-deficient monosomic cell lines, we find t...

    Narendra Kumar Chunduri, Paul Menges, **aoxiao Zhang in Nature Communications (2021)

  5. Article

    Open Access

    The p53/p73 - p21CIP1 tumor suppressor axis guards against chromosomal instability by restraining CDK1 in human cancer cells

    Whole chromosome instability (W-CIN) is a hallmark of human cancer and contributes to the evolvement of aneuploidy. W-CIN can be induced by abnormally increased microtubule plus end assembly rates during mitos...

    Ann-Kathrin Schmidt, Karoline Pudelko, Jan-Eric Boekenkamp, Katharina Berger in Oncogene (2021)

  6. Article

    Open Access

    DNA replication stress mediates APOBEC3 family mutagenesis in breast cancer

    The APOBEC3 family of cytidine deaminases mutate the cancer genome in a range of cancer types. Although many studies have documented the downstream effects of APOBEC3 activity through next-generation sequencin...

    Nnennaya Kanu, Maria Antonietta Cerone, Gerald Goh in Genome Biology (2016)

  7. Article

    Open Access

    Learning (from) the errors of a systems biology model

    Mathematical modelling is a labour intensive process involving several iterations of testing on real data and manual model modifications. In biology, the domain knowledge guiding model development is in many c...

    Benjamin Engelhardt, Holger Frőhlich, Maik Kschischo in Scientific Reports (2016)

  8. No Access

    Book

  9. No Access

    Chapter

    Membrane Transport in Yeast, An Introduction

    Research on membrane transport has made continuous progress in the last decades and remains an active field of scientific investigation. In the case of yeast, most of the research has been conducted for the mo...

    Maik Kschischo, José Ramos, Hana Sychrová in Yeast Membrane Transport (2016)

  10. No Access

    Chapter

    Mathematical Modelling of Cation Transport and Regulation in Yeast

    Mathematical modelling of ion transport is a strategy to understand the complex interplay between various ionic species and their transporters. Such models should provide new insights and suggest new interesti...

    Matthiasé Kahm, Maik Kschischo in Yeast Membrane Transport (2016)

  11. No Access

    Article

    Expression of regulators of mitotic fidelity are associated with intercellular heterogeneity and chromosomal instability in primary breast cancer

    Regulators of transition through mitosis such as SURVIVIN and Aurora kinase A (AURKA) have been previously implicated in the initiation of chromosomal instability (CIN), a driver of intratumour heterogeneity. ...

    Rebecca Roylance, David Endesfelder in Breast Cancer Research and Treatment (2014)

  12. Article

    Correction: Corrigendum: Replication stress links structural and numerical cancer chromosomal instability

    Nature 494, 492–496 (2013); doi:10.1038/nature11935 In this Letter we inadvertently omitted full details of The Cancer Genome Atlas data sets. The Acknowledgements should have included these sentences: “The re...

    Rebecca A. Burrell, Sarah E. McClelland, David Endesfelder, Petra Groth in Nature (2013)

  13. No Access

    Article

    Replication stress links structural and numerical cancer chromosomal instability

    A mechanism to explain chromosomal instability (CIN) in colorectal cancer is demonstrated; three new CIN-suppressor genes (PIGN, MEX3C and ZNF516) encoded on chromosome 18q are identified, the loss of which leads...

    Rebecca A. Burrell, Sarah E. McClelland, David Endesfelder, Petra Groth in Nature (2013)

  14. No Access

    Article

    How dynamical models can learn from the data—an example with a simplified ENSO model

    Most dynamical models of the natural system contain a number of empirical parameters which reflect our limited understanding of the simulated system or describe unresolved subgrid-scale processes. While the pa...

    Heiko Paeth, Janna Lindenberg, Maik Kschischo in Theoretical and Applied Climatology (2011)

  15. No Access

    Article

    Ring test assessment of the mKir2.1 growth based assay in Saccharomyces cerevisiae using parametric models and model-free fits

    Inward rectifying K+ (Kir) channels are a subfamily of the potassium channel superfamily. They mediate potassium influx into the cells, a process responding to the polarization state, a variety of intracellular m...

    Guido Hasenbrink, Lucie Kolacna, Jost Ludwig in Applied Microbiology and Biotechnology (2007)

  16. No Access

    Article

    Automatic Scoring and Quality Assessment Using Accuracy Bounds for FP-TDI SNP Genoty** Data

    Background: Human diversity, namely single nucleotide polymorphisms (SNPs), is becoming a focus of biomedical research. Despite the binary nature of SNP determination, the majority of genoty** ...

    Maik Kschischo, Rainer Kern, Christian Gieger, Martin Steinhauser in Applied Bioinformatics (2005)

  17. No Access

    Article

    Toward an accurate statistics of gapped alignments

    Sequence alignment has been an invaluable tool for finding homologous sequences. The significance of the homology found is often quantified statistically by p-values. Theory for computing p-values exists for gapl...

    Maik Kschischo, Michael Lässig, Yi-Kuo Yuc in Bulletin of Mathematical Biology (2005)