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Real-time Quantification of HER2/neu Gene Amplification by
Real-time Quantification of HER2/neu Gene Amplification by

... The techniques used to evaluate the HER2/neu gene status have included gene-based assays such as Southern and slot blotting, in-situ hybridization (fluorescent and nonfluorescent) and PCR methods [7]. Each of the techniques mentioned has its advantages and disadvantages. In order to perform a fast p ...
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... Copyright © 2007 by Pearson Education, Inc. Publishing as Benjamin Cummings ...
Molecular Structure of the GARP Family of Plant Myb
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... assay was performed with a set of synthetic 34-bp oligonucleotides, each containing the core sequence (AGAT) or its variant (GGAT), as shown in Figure 5A. The presumed minimum DNA binding domain of 64 amino acids (i.e., ARR10-B) was used for the gel-shift assays. The results are shown in Figure 5A. ...
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... those of the Z curve method (33 parameters) which Guo et al. used to recognize protein-coding genes in bacterial and archaeal genomes [1]. It means that our method proposed here is comparable with the best existing methods for the gene finding problem. The main aim of this work is to develop efficie ...
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RSC Communication Template (Version 3.1)
RSC Communication Template (Version 3.1)

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On-going effort by a Cambodian expert to apply the GPG
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Chpt7_RepairDNA.doc
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chapter 7 mutation and repair of dna
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... Question 7.5. Both hypoxanthine and xanthine can base pair with cytosine in DNA. Why is this? Oxidation of C to U occurs spontaneously at a high rate. The frequency is such that 1 in 1000 Cs in the human genome would become Us during a lifetime, if they were not repaired. As will be discussed later, ...
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Ch 8 Workbook Answer Key

... One of the earliest was done by Frederick Griffith who was studying two forms of the bacterium that causes pneumonia. The S form was surrounded by a coating that made them look smooth. The R form did not have a coating, and the colonies looked rough. Griffith injected these bacteria into mice and fo ...
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... asymptomatic father in this family. Thus it is highly likely that the O4 deletion is responsible for EPP in this family. Our expression studies in E. coli cells clearly showed that the mutant ferrochelatase with the O4 deletion was translated as no immunologically detectable protein or enzyme activi ...
Reaction of Systemic Lupus Erythematosus Antinative DNA
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... NaOH and reneutralized, and electrophoresis was run for 2.5 h at 75 mA. The OX174 RF HINC II digest was also denatured. were denatured by the addition of NaOH to a final concentration of 0.1 N, reneutralized, and examined ...
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... one amino acid. This is not true of the genetic code, i.e., there is no ambiguity. Amino acid – one of twenty monomers of proteins. Each of them have a central carbon atom surrounded by an amine group, a carboxyl group, a hydrogen atom and a side group (referred to as the “R-group” that is unique to ...
PDF - Oxford Academic - Oxford University Press
PDF - Oxford Academic - Oxford University Press

... 96% of amino acid residues. These assignments allowed chemical shift changes upon DNA binding to be mapped to specific regions of the protein backbone. Similar chemical shift mapping strategies have been widely used to localise intermolecular binding surfaces in other DNA/protein systems (31–33). In ...
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Microsatellite



A microsatellite is a tract of repetitive DNA in which certain DNA motifs (ranging in length from 2–5 base pairs) are repeated, typically 5-50 times. Microsatellites occur at thousands of locations in the human genome and they are notable for their high mutation rate and high diversity in the population. Microsatellites and their longer cousins, the minisatellites, together are classified as VNTR (variable number of tandem repeats) DNA. The name ""satellite"" refers to the early observation that centrifugation of genomic DNA in a test tube separates a prominent layer of bulk DNA from accompanying ""satellite"" layers of repetitive DNA. Microsatellites are often referred to as short tandem repeats (STRs) by forensic geneticists, or as simple sequence repeats (SSRs) by plant geneticists.They are widely used for DNA profiling in kinship analysis and in forensic identification. They are also used in genetic linkage analysis/marker assisted selection to locate a gene or a mutation responsible for a given trait or disease.
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