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CHO-human hybrid cells as models for human chromosome non-disjunctionEvans, Elizabeth Balconi 02 May 2009 (has links)
We have used Chinese hamster ovary (CHO)-human hybrid cells containing chromosomes 16, 18, X, and 21 to test the ability of human kinetochores to successfully bind to spindle microtubules and to be distributed to the daughter cells. We have established the intrinsic rate of non-disjunction among these human chromosomes noted above and compared these rates with those in cells presented with mitotic challenges such as taxol, nocodazole, and mitosis with unreplicated genomes (MUG). Cells were grown on culture slides, fixed and processed for immunofluorescence and fluorescence in situ hybridization (FISH). Daughter pairs were identified by staining with anti-á-tubulin to identify midbodies. Human centromere DNA probes were used for FISH in order to test for the successful passage of human kinetochores to daughter cells during anaphase. Our data indicate that different human kinetochores vary in their ability to properly engage the spindle and to be successfully distributed. In addition, mitotic challenges have been shown to affect the rate of non-disjunction. The mechanism of this effect is not yet known.
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The Mammalian Process of Meiotic SynapsisBrown, Petrice Wynaka January 2007 (has links)
No description available.
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Transgenerational Genetic Effects In Mouse Models Of Complex TraitsNelson, Vicki R. January 2010 (has links)
No description available.
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X Chromosome Aneuploidy: A Look at the Effects of X InactivationSprong, Amy Nicole 26 April 2008 (has links)
No description available.
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Evaluation of Soybean Germplasm for Additional Sources of Resistance and Characterization of Resistance towards Fusarium graminearum.Acharya, Bhupendra 03 November 2014 (has links)
No description available.
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THE REGULATION OF BubR1 EXPRESSION BY p53: A ROLE FOR p53 IN THE MITOTIC SPINDLE CHECKPOINT AND CHROMOSOME INSTABILITYSTUABACH, AMY ELIZABETH January 2004 (has links)
No description available.
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Immune Defects in Chromosome 22q11.2 Deletion SyndromesBobey, Nicola A. 08 April 2010 (has links)
No description available.
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Chromosomal abnormalities identified in infants with congenital heart diseaseConnor, Jessica 04 August 2011 (has links)
No description available.
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Molecular and Integrated Systems Physiology of ProlactinChristensen, Heather R. 23 September 2011 (has links)
No description available.
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Genomic signatures of population history in a pair of recently diverged Australian teal support strong selection on the Z - sex chromosomeHawkins, Kevin Kyle 30 August 2016 (has links)
No description available.
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