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CLASSIFYING CANCER GENES
CLASSIFYING CANCER GENES

... collaborative, online building of a data set accomplished by the students and the genome analysis done by the researchers (on a larger scale). Students could post their 3-2-1 analyses as blog posts (on a class blog or individual student blogs). Once posted, the comments feature could be used to faci ...
Reading Guide for Chapter 10
Reading Guide for Chapter 10

... 4. What is the human female gamete? ______________ Is it haploid or diploid? ______________ 5. What is the human male gamete? ________________ Is it haploid or diploid? _______________ 6. Why does meiosis have to occur? _______________________________________________________ 7. Why is it called sexu ...
GENETICS OF CONTINUOUS VARIATION
GENETICS OF CONTINUOUS VARIATION

... far beyond the limits of the variability of the original series. Both extremes, when crossed to self-colored rats, gave self (that is, uniformly colored) in F1, and 3 self to 1 hooded in F2. Castle argued that this pointed to a gradual change in the hooded gene, rather than to an accumulation of mod ...
DNA Extraction Lab
DNA Extraction Lab

Sex and the genome
Sex and the genome

... high conformational flexibility, are very different and probably confer unique properties on each sHSP. The fact that mutations in different sHSPs are associated with similar, but not identical, diseases support this idea of distinct roles for these proteins. Moreover, the relatively late onset of s ...
Ch .15 - Crestwood Local Schools
Ch .15 - Crestwood Local Schools

... Could produce 38,000 different polypeptides Many of these polypeptides have been found ...
Transcript
Transcript

... Tumor progression. Subclones are generated from the original malignant cells. The most fit survive and predominate in the tumor. The rate at which subclones with additional phenotypes develop is variable. ...
Gene Mutations
Gene Mutations

... Xeroderma Pigmentosum ...
pdf
pdf

... provide a polyploid clade with the potential to radiate. Polyploidy is important for the generation of genetic and genomic novelty, but it also requires extensive genome reorganization in order for this evolutionary potential to be fully realized (i.e. ‘diploidization’). Over intermediate timescales ...
O - Faculty Web Pages
O - Faculty Web Pages

... Xeroderma Pigmentosum ...
Mendelian Genetics
Mendelian Genetics

... Recessive allele: the allele that is NOT expressed if there is a dominant allele present. (Use a small letter). ...
History—One gene, one polypeptide hypothesis The Overall
History—One gene, one polypeptide hypothesis The Overall

... RNA polymerase is the kind of enzyme that joins ribonucleotides to make all the kinds of RNA. RNA polymerase finds the promoter region of a gene with help from transcription factor polypeptides which in turn are signaled by the cell to recognize particular genes. RNA polymerase binds to the DNA doub ...
Deriving Trading Rules Using Gene Expression Programming
Deriving Trading Rules Using Gene Expression Programming

... due to the various flavors of operators that take different numbers of arguments and have different return types. This variety generates numerous restrictions when applying crossover and mutation like operations, as syntax trees must be kept valid after transformations are made. A criticism of genet ...
Lecture 8 Annotating Gene Lists
Lecture 8 Annotating Gene Lists

... chromosome location, KEGG pathways, transcription factor or microRNA target genes ...
to view the Abstract Guidelines
to view the Abstract Guidelines

... immunogenicity, pathogenicity and the limited size of therapeutic DNA which can be incorporated into the viral genome. Nonviral approaches are not subject to these problems but, thus far, have proven inefficient in delivering therapeutic DNA to the nucleus. We have used various approaches to optimis ...
nature | methods Versatile P[acman] BAC libraries for transgenesis
nature | methods Versatile P[acman] BAC libraries for transgenesis

... was used to innoculate a secondary culture, induce high plasmid copy number, and perform paired end sequencing, as described above. Two plasmid DNA preparation methods were used; these can be substituted. For CHORI322 clones, cultures were induced to high plasmid copy number with CopyControl™ Fosmid ...
here
here

... substitutions for genes found only in the E.coli Salmonella clade is lower than 1, but larger than for more widely ...
genotype–phenotype correlation difficult. As far as we know, this is
genotype–phenotype correlation difficult. As far as we know, this is

... the 33K tiling BAC array and of the proband by 2.7M high-resolution oligonucleotide array painting did not reveal additional genomic variation. Furthermore, mutation screening of the TRPS1 also did not reveal any alteration. Finally, expression studies of TRPS1 performed from LCLs indicate that inte ...
Mendelian Genetics Part 1
Mendelian Genetics Part 1

... 2. Genes can be of alternate forms called alleles. E.g. one form of the gene that determines pod color was green; the other was yellow. ...
dsRNA synthesis RNAi (Howard Clarke)
dsRNA synthesis RNAi (Howard Clarke)

... Selection and preparation of DNA template: Chose an exon-rich region of genomic DNA 300bp in length (>500 is better, and 3’ UTR sequence is fine). Alternatively, cDNA clones or first-strand cDNA generated by RT-PCR can be used as template (see protocol “Oligo d(T) primed cDNA synthesis”). cDNA templ ...
Efficient TALEN-mediated gene targeting of chicken
Efficient TALEN-mediated gene targeting of chicken

... To target the DDX4 locus we utilised TALEN-stimulated HDR to recombine a GFP2a-puromycin transgene targeting vector into the DDX4 locus, replacing exon 2 and 3 of the endogenous DDX4 locus (Fig. 1A). A TALEN pair was designed that cleaved exon 2 of the DDX4 locus immediately downstream of the ATG st ...
Table 7. Summary statistics for the consensus gene set of Haliotis
Table 7. Summary statistics for the consensus gene set of Haliotis

... discus hannai was 1.86 Gb, and this is the biggest genome among known gastropods. It is 5.31 and 2.02 times larger than genomes size of L.gigantea (0.35 Gb) and A.californica (0.92 Gb) in the same Gastropoda class. In animals, the increase of genome size is commonly driven by transposable element, ...
Supplementary Text 1 (doc 52K)
Supplementary Text 1 (doc 52K)

... Sequencing of 16S rRNA genes and phylogenetic analysis PCR products were sequenced using the DYEnamic Direct cycle sequencing kit (Amersham Life Science) and a Model 4200 automated DNA sequencer (LI-COR) as described by Rink et al. (2007). Sequences were analysed by BLASTn search (http://www.ncbi.n ...
principles of genetics
principles of genetics

... divides to produce two new cells, each containing an exact copy of the DNA of the parent cell. Candidates should be able to name and explain the stages of mitosis and recognise each stage from diagrams and photographs. ...
17.1 – Isolating the Genetic Material
17.1 – Isolating the Genetic Material

... renders a gene unable to code for any functional polypeptide product 2) frame-shift mutation – permanent change in the genetic material of a cell caused by the insertion or deletion of one or two nucleotides within a sequence of codons. Usually, a frame-shift causes a nonsense mutation (see fig 17.3 ...
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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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