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PowerPoint® slides
PowerPoint® slides

... LIMITED TO THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE. University will not be liable for any costs, damages, fees or other liability, nor for any direct, indirect, special, incidental or consequential damages (including lost profits) with respect to any claims by ...
Cool Stuff About DNA
Cool Stuff About DNA

... More than 200 genes in the human genome have a bacterial ancestry. ...
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... person, [which can then be used to distinguish that persons DNA from other DNA] One allele masks the expression of the other. Biological catalyst ...
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... cell division, this can result in cancer or genetic defects such as trisomy 21. Therefore, to ensure safe transport of DNA during cell division the long and coiled DNA fibers must be tightly packed. Scientists have only a sketchy understanding of this step. The SMC-kleisin protein complexes play a k ...
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... Microarrays can be used to study the expression of genes and compare patterns between healthy and unhealthy cells. It is the mRNA from cells which is used to form labelled probes (after it has been copied into single stranded DNA). ...
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< 1 ... 323 324 325 326 327 328 329 330 331 ... 356 >

Epigenomics

Epigenomics is the study of the complete set of epigenetic modifications on the genetic material of a cell, known as the epigenome. The field is analogous to genomics and proteomics, which are the study of the genome and proteome of a cell (Russell 2010 p. 217 & 230). Epigenetic modifications are reversible modifications on a cell’s DNA or histones that affect gene expression without altering the DNA sequence (Russell 2010 p. 475). Two of the most characterized epigenetic modifications are DNA methylation and histone modification. Epigenetic modifications play an important role in gene expression and regulation, and are involved in numerous cellular processes such as in differentiation/development and tumorigenesis (Russell 2010 p. 597). The study of epigenetics on a global level has been made possible only recently through the adaptation of genomic high-throughput assays (Laird 2010) and.
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