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16 Mustafa Saffarini NOOR MA`ABREH PATHOLOGY Mazen al
16 Mustafa Saffarini NOOR MA`ABREH PATHOLOGY Mazen al

... Whether this is a cause or an effect of the original insult, we don’t know. There are two possibilities: a. Mitotic checkpoint failure leads to Aneuploidy. b. Aneuploidy leads to mitotic checkpoint failure and over expression. Because now there is an abnormal number of genes in the cell (these cells ...
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...  The repair enzymes go to work, cutting out a chunk from one side of the DNA containing the mistake. Then new enzymes, using the base pairing code, make a new side from the opposite strand of DNA.  The new strand is put into place by another enzyme system. ...
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... erosion at cell divisions, chromosomal non-homologous end-joinings and nuclease attacks. ...
recombinant dna technology
recombinant dna technology

... • FIRST, THE PLASMID IS TREATED WITH THE SAME RESTRICTION ENZYME AS WAS USED TO CREATE THE DNA FRAGMENT • THE RESTRICTION ENZYME WILL CUT THE PLASMID AT THE SAME RECOGNITION SEQUENCES, PRODUCING THE SAME STICKY ENDS CARRIED BY THE FRAGMENTS • MIXING THE FRAGMENTS WITH THE CUT PLASMIDS ALLOWS BASE-PA ...
State-of-the-art Biological Processes Enrichment Using Gene Ontology
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Unit 5 vocab
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... - What kind of mutations can happen to DNA (i.e. a nucleotide is deleted)? Deletion, insertion. - Do all mutations result in a faulty protein? Why or why not? No, because if you make mRNA that codes for same amino acids, you will end up with the same protein. This happens because some codons code fo ...
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... Tay-Sachs disease is a fatal genetic lipid storage disorder in which harmful quantities of a fatty substance called ganglioside GM2 build up in tissues and nerve cells in the brain. The condition is caused by insufficient activity of an enzyme called beta-hexosaminidase A that catalyzes the biodegra ...
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... • The physical features of the two orphan girls were determined by a particular assortment of genes. • Perhaps one of the girls had brown eyes and, since genes come in pairs, let us refer to these genes as BB. The capital В is used because the gene for brown eyes is a dominant gene, meaning that it ...
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... the high expression level of the -gene and that the -fusion mRNA is less stable than the mRNA, which would explain the moderate increase in HbA2 (12). For case 2 and 3 gene rearrangement results in loss of one  gene. This explains the unexpectedly low level of HbA2 observed in both cases. The h ...
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... serine proteases, which have strong fibrinolytic and thrombolytic activities. The proteases have the abilities not only to hydrolyze fibrin and other proteins, but also activate proenzymes such as plasminogen and prothrombin11. Compared to the present thrombolytic drugs, earthworm fibrinolytic enzym ...
The Chromosome Theory of Inheritance
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... Morgan’s Experimental Evidence: Scientific Inquiry •Thomas Hunt Morgan: A. first to observe and note genes and chromosomes move together B. provided convincing evidence Mendel’s heritable factors are on chromosomes C. worked with fruit flies – Why? breed at a high rate new generation every 2 weeks o ...
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Chapter 12 Cell Cycle Functions of cell division. . Phases of the cell

... DNA as the Genetic Material 1. Read the contributions of various scientist in history of DNA given in notes. Griffith’s transformation experiment. 2. What was the experimental evidence that helped Watson and Crick to propose the structure of DNA. 3. Describe the structure of DNA (base-pairing rule, ...
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Site-specific recombinase technology



Nearly every human gene has a counterpart in the mouse (regardless of the fact that a minor set of orthologues had to follow species specific selection routes). This made the mouse the major model for elucidating the ways in which our genetic material encodes information. In the late 1980s gene targeting in murine embryonic stem (ES-)cells enabled the transmission of mutations into the mouse germ line and emerged as a novel option to study the genetic basis of regulatory networks as they exist in the genome. Still, classical gene targeting proved to be limited in several ways as gene functions became irreversibly destroyed by the marker gene that had to be introduced for selecting recombinant ES cells. These early steps led to animals in which the mutation was present in all cells of the body from the beginning leading to complex phenotypes and/or early lethality. There was a clear need for methods to restrict these mutations to specific points in development and specific cell types. This dream became reality when groups in the USA were able to introduce bacteriophage and yeast-derived site-specific recombination (SSR-) systems into mammalian cells as well as into the mouse
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