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Dynamic Model of Paclitaxel Biosynthesis Suggests That the Key
Dynamic Model of Paclitaxel Biosynthesis Suggests That the Key

... pathways: MVA pathway in cytosol and MEP/DXP pathway in plastid. ...
Retrogenes reveal the direction of sex-chromosome
Retrogenes reveal the direction of sex-chromosome

... Heteromorphic sex chromosomes, both XX/XY and ZZ/ZW systems, have evolved independently multiple times in both animals and plants (BULL 1983; CHARLESWORTH 1996; RICE 1996). Sex chromosomes are thought to evolve from a pair of autosomes that acquire a new sex-determining locus. Theory suggests that ...
Single nucleotide polymorphism in coronary
Single nucleotide polymorphism in coronary

... ISR and require further investigation, also by means of genetic analysis from large cohorts of patients worldwide. Already provided data support the thesis of genetic background of higher susceptibility to CAD itself, some to atherosclerosis, also located in other than coronary vessels, but ISR is s ...
S0735109712013162_mmc1
S0735109712013162_mmc1

... Additional loci for clopidogrel ...
oculocutaneous albinism and analysis of tyrosinase gene in
oculocutaneous albinism and analysis of tyrosinase gene in

... patients. One is allele-specific amplification based on the specific amplification of the target allele by a PCR with the normal and mutant allele-specific modified primers inhibiting unfavorable amplification. 15) The other is successful sequence analysis of all amplified exons of the tyrosinase ge ...
The case for transgenerational epigenetic inheritance in humans
The case for transgenerational epigenetic inheritance in humans

Age study
Age study

... accurately describe the variables that affect the response variables (gene expression). Thus, by incorporating the same variables into the ANOVA that are affecting the microarray data, the technical effects can be accounted for, and the biologically relevant effects become more apparent. Additionall ...
Differential Expression Analysis
Differential Expression Analysis

... Suppose that 1000 genes are represented on an array and we test each with a t test with a Type I error threshold of 0.05. We might expect 40 genes to be differentially expressed. Of the 960 non-differentially expressed genes we can expect 5% errors, or .05 × 960 = 48 false positives. In other words, ...
Activation of the JNK pathway during dorsal closure in Drosophila
Activation of the JNK pathway during dorsal closure in Drosophila

TregouetD_EGEE3-presentation
TregouetD_EGEE3-presentation

... • Genome Wide Haplotype Association Studies are now a reality thanks to the use of Grid technology • Using EGEE, we were able to identify a cluster of 3 genes where haplotypes are strongly associated with CAD risk (Tregouet et al. Nature Genetics March 2009) • Possibility to apply such tool to other ...
The Clinical Spectrum - American Diabetes Association
The Clinical Spectrum - American Diabetes Association

... a few months but may reappear months or years later. The other 50% have permanent NDM (PNDM). In a small percentage of these, diabetes is part of a complex clinical syndrome involving organs other than the endocrine pancreas. For those with isolated PNDM, mutations in four different genes have been ...
Mendel’s Laws and Genetics Douglas Wilkin, Ph.D. Jean Brainard, Ph.D.
Mendel’s Laws and Genetics Douglas Wilkin, Ph.D. Jean Brainard, Ph.D.

... The expression of an organism’s genotype produces its phenotype. The phenotype refers to the organism’s characteristics, such as purple or white flowers. As you can see from Table 1.1, different genotypes may produce the same phenotype. For example, BB and Bb genotypes both produce plants with purpl ...
Professor Anthony Monaco - AWARES, the All Wales Autism Resource
Professor Anthony Monaco - AWARES, the All Wales Autism Resource

... families -Rare mutations identified: NLGN, NRXN, SHANK3 •Common Disease, Common Variant model -High Resolution SNP/haplotype association mapping -Regional or Whole Genome Association studies ...
glycan associated protein of Legionella (PpiA)
glycan associated protein of Legionella (PpiA)

... for the evaluation of diagnostic DNA probes. lt is of interest that the Cla I hybridization pattern of the strains exhibited heterogeneity to some degree and that the cloned 1.8 kb Cla I fragment was not present in this size in the original strain L. pneumophila, P-hiladelphia 1. Differences in DNA ...
chapter thirteen
chapter thirteen

... The number of combinations possible when chromosomes assort independently into gametes is 2n, where n is the haploid number of the organism.  If n = 3, there are 23 = 8 possible combinations.  For humans with n = 23, there are 223, or more than 8 million possible combinations of chromosomes. ...
13_DetailLectOut_AR
13_DetailLectOut_AR

... The number of combinations possible when chromosomes assort independently into gametes is 2n, where n is the haploid number of the organism.  If n = 3, there are 23 = 8 possible combinations.  For humans with n = 23, there are 223, or more than 8 million possible combinations of chromosomes. ...
Document
Document

... Consider the codons specifying aspartic acid and lysine: both start AA, lysine ends A or G, and aspartic acid ends T or C. So, if the rate at which C changes to T is higher from the rate that C changes to G or A (as is often the case), then more of the changes at the third position will be synonymou ...
Differential Regulation of Antagonistic Pleiotropy in Synthetic and
Differential Regulation of Antagonistic Pleiotropy in Synthetic and

... specific (a locus with an effect in only one environment), scale (a similar effect but varying in ...
Contrasting Properties of Gene-Specific Regulatory, Coding, and
Contrasting Properties of Gene-Specific Regulatory, Coding, and

... either the expression or function of a gene product can contribute to phenotypic evolution; mutations that alter gene copy number have also been shown to be an important source of phenotypic variation. Predicting when and why one type of mutation is more likely to underlie a phenotypic change than a ...
Comparative Genomic Hybridization in Chronic B
Comparative Genomic Hybridization in Chronic B

X-chromosome inactivation and its implications for human
X-chromosome inactivation and its implications for human

... cleavage stage embryos comparable to the mouse23, whereas another study found XCI-initiation on both Xchromosomes at the blastocyst stage without silencing, which only occurs at later stages on a single Xchromosome24. A recent study has used in vitro culture of human embryos on decidualized endometr ...
Why do more divergent sequences produce smaller non
Why do more divergent sequences produce smaller non

... amino acids (BAUD and K ARLIN 1999). The active site of an enzyme may only tolerate very few different amino acids that can stabilize a particular substrate and carry out an enzymatic reaction. Halpern and Bruno (1998; see also TAMURI et al. 2012) proposed a codon substitution model based on a popul ...
Laws of Inheritance
Laws of Inheritance

... R allele for the seed shape gene and either a Y or a y allele for the seed color gene. It R and an r allele; each gamete can have only one allele per gene. The law of independent assortment states that a gamete into which an r allele is sorted would be equally likely to contain either a Y or a y all ...
Cot-1 banding of human chromosomes using fluorescence
Cot-1 banding of human chromosomes using fluorescence

... labeling. Clear green signals of probe DNA on the red banded chromosomes can be obtained and the banding resolution is as clear as Q-banding. By this method, we mapped a 4-kb genomic DNA fragment from myelin protein zero (MPZ) gene on chromosome 1q22 to q23 (Fig. 4) that is consistent with our previ ...
Multiple domestications of Asian rice
Multiple domestications of Asian rice

... of a π(wild)/π(domesticated) threshold of 4 for each of japonica, indica and aus, and implied that a higher threshold would be more appropriate for the detection of selective sweeps in japonica. In fact, we tested the data with such approach – we described it in the first paragraph of our methods, a ...
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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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