Assays for mitotic chromosome condensation in live yeast and mammalian cells
Chromosome Research, ISSN: 0967-3849, Vol: 17, Issue: 2, Page: 145-154
2009
- 3Citations
- 55Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations3
- Citation Indexes3
- CrossRef3
- Captures55
- Readers55
- 55
Review Description
The dynamic reorganization of chromatin into rigid and compact mitotic chromosomes is of fundamental importance for faithful chromosome segregation. Owing to the difficulty of investigating this process under physiological conditions, the exact morphological transitions and the molecular machinery driving chromosome condensation remain poorly defined. Here, we review how imaging-based methods can be used to quantitate chromosome condensation in vivo, focusing on yeast and animal tissue culture cells as widely used model systems. We discuss approaches how to address structural dynamics of condensing chromosomes and chromosome segments, as well as to probe for mechanical properties of mitotic chromosomes. Application of such methods to systematic perturbation studies will provide a means to reveal the molecular networks underlying the regulation of mitotic chromosome condensation. © 2009 Springer Science+Business Media B.V.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=63049115934&origin=inward; http://dx.doi.org/10.1007/s10577-008-9010-1; http://www.ncbi.nlm.nih.gov/pubmed/19308697; http://link.springer.com/10.1007/s10577-008-9010-1; https://dx.doi.org/10.1007/s10577-008-9010-1; https://link.springer.com/article/10.1007/s10577-008-9010-1; http://www.springerlink.com/index/10.1007/s10577-008-9010-1; http://www.springerlink.com/index/pdf/10.1007/s10577-008-9010-1
Springer Science and Business Media LLC
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