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Nonstationary Functional Optimization
Nonstationary Functional Optimization

... In each generation the best and the average tness are reported as performance measures. The two problems were run independently. Figure 2 & gure 3 show the best-ofgeneration and the generation average results of the rst problem (table 1), and gure 4 & gure 5 give the corresponding results of th ...
Abstract/Session Information for Program Number 1264
Abstract/Session Information for Program Number 1264

... SNP analysis of control and CCD subjects and cross species sequence analysis, we have identified conserved GATA domain binding sites in the RUNX2 promoter. Because TRPS1 is the only GATA domain transcription factor known to function in skeletogenesis, we analyzed its expression pattern during mouse ...
Molecular Testing Applications in Coagulation
Molecular Testing Applications in Coagulation

... • AT deficiency = up to 16-fold increase in risk of VTE and may manifest heparin resistance • Acquired deficiencies of protein C and protein S may occur in association with vitamin K deficiency ...
Information Encoding in Biological Molecules: DNA and
Information Encoding in Biological Molecules: DNA and

... other tracks are available Lab 7.2 ...
Nature Genetics - Community Capability Model
Nature Genetics - Community Capability Model

... Nature quality primary research in genetics and genomics - Professional editors choose which papers to publish - Peer referees provide technical guidance to improve the work - Editorial standards and decision criteria are constantly revised in light of referee advice, author comments, conference pr ...
A global view of pleiotropy and phenotypically
A global view of pleiotropy and phenotypically

... groups with more complex phenotype profiles (Figure 2B), but with equally specific functional enrichments as the gene sets constructed from low-pleiotropy mutants. Consistent with recently published results (Parsons et al, 2004), many of the clusters that include conditions with drugs added to the m ...
PHAR2811 Dale`s lecture 7 The Transcriptome Definitions: Genome
PHAR2811 Dale`s lecture 7 The Transcriptome Definitions: Genome

... • The 3’ end of the tRNAs all have a CCA, some of which are attached after cleavage (some have the sequence encoded in the DNA). The attachment is done by a special enzyme. • The CCA is important as this is where the amino acid is attached. • Several of the bases e.g. pseudouracils in tRNA molecules ...
Evolution of Mammalian KELL Blood Group Glycoproteins and
Evolution of Mammalian KELL Blood Group Glycoproteins and

... may result in severe hemolytic transfusion reactions and hemolytic disease of the fetus and newborn [5,7]. Recent studies have suggested that these reactions may occur not only as a result of immune RBC destruction, but also by the suppression of erythropoiesis by antiKELL-K1 antibodies, which can l ...
ppt - Chair of Computational Biology
ppt - Chair of Computational Biology

... between the genes associated with each such junction were calculated. The junctions were grouped according to the directionality of the reactions, as shown. Divergent junctions, which allow the flow of metabolites in two alternative directions, predominantly show a linear coregulation pattern, where ...
Solving the University Timetabling Problem with
Solving the University Timetabling Problem with

... tors for self-adaptation of genetic algorithms that is suitable for solving the university timetabling problem. Comparing to previous approaches (e.g. [2], [12], [20]) we designed the encoding for self-adaptation not only one parameter but for all or nearly all possible parameters of genetic algorit ...
Gene Section FANCE  (Fanconi  anemia,  complementation  group E)
Gene Section FANCE (Fanconi anemia, complementation group E)

Slides PPT
Slides PPT

... material, stored as DNA. • The nuclear genome refers to the DNA in the chromosomes contained in the nucleus; in the case of humans the DNA in the 46 chromosomes. It is the nuclear genome that defines a multicellular organism; it will be the same for all (almost) cells of the organism. ...
Slide 1
Slide 1

... For at least 5% of all clinically recognized human pregnancies, meiotic segregation errors give rise to zygotes with the wrong number of chromosomes. Although most aneuploid fetuses perish in utero, trisomy in liveborns is the leading cause of mental retardation. A large percentage of human trisomie ...
not a plastid specific promoter but is also capable of
not a plastid specific promoter but is also capable of

... Analysis of PAT activity of transgenic SRI carrying T-DNAs of pGSC65, pGSC65 -1, pGSC65 -2 and pGSC54 revealed that only transgenic plants carrying the intact psbA region express PAT to a detectable level (table 1). This indicates the functional importance of both the CAAT and the TATA region for PA ...
Genetics and Genomics
Genetics and Genomics

... 2.4.4. Double-Y syndrome, "superman" or Jacobs syndrome .............................. 39 3. Uniparental disomy (UPD) ................................................................................................. 39 4. Mixoploid mutations .......................................................... ...
Gene Section PAX2 (Paired box gene 2) Atlas of Genetics and Cytogenetics
Gene Section PAX2 (Paired box gene 2) Atlas of Genetics and Cytogenetics

Personnel changes should be notified to GMSO
Personnel changes should be notified to GMSO

...  does insertion of foreign gene alter pathogenicity of host through complementation/ transcriptional effects ?  does the inserted DNA encode a toxin, oncogenic protein, allergen, hormone, cytokine, antibiotic resistance factor or any other protein with a potentially harmful biological activity ?  ...
Cell Division Studies of Escherichia Coli: Expression and Protein
Cell Division Studies of Escherichia Coli: Expression and Protein

... Progress has been made in understanding cell division at the genetic level. Conditional lethal mutants that cannot form septa have been isolated and referred to as filamentation temperature-sensitive (fts) mutants. septum are ...
Massive Changes in Genome Architecture Accompany
Massive Changes in Genome Architecture Accompany

... codons and, in a branch-specific analysis using PAML, a higher dN/dS ratio along the N. tetrasperma branch for the genes in the nonrecombining region compared to their N. crassa and N. discreta orthologs. However, these analyses assume that the location and number of nonrecombining strata in their li ...
E45
E45

... breeding. Since the inheritance of these traits is different from that of quantitative traits in a traditional sense, the classic analysis methods are no longer valid for them. There need to be appropriate methods for obtaining correct genetic conclusions. As reviewed by Gilbert (1985b), single locu ...
File - Mr. Shanks` Class
File - Mr. Shanks` Class

... Mendel allowed the ______ plants to mature and self-pollinate. Their offspring were called the __________ ________ ___________ (___) Mendel's Observations: _______of the plants were tall, _______ of the plants were short Mendel's Conclusion: Offspring inherit two __________ for each characteristic ( ...
Enhanced Detection of Longer Insertions and Deletions in Clinical
Enhanced Detection of Longer Insertions and Deletions in Clinical

... found in the human genome and substantial amount of research, such as that by the International HapMap Consortium, has been focused on accurately mapping and identifying SNVs for human genetic variation studies [8]. However, in spite of being the second most common type of genomic alterations [9], i ...
Extrachromosomal DNA Transformationof Caenorhabditis elegans
Extrachromosomal DNA Transformationof Caenorhabditis elegans

... amount of pBR322 hybridization expected for each worm DNA preparation if the plasmid sequences were present in one copy per genome (see Table 2). The percentage of transformed worms in each population was used to derive the copy number per genome per transformant. It should be noted that the copy nu ...
supplementary material
supplementary material

... conditional TERT activation affects telomere function, we derived mouse embryo fibroblasts (MEFs) and splenocytes from i-TERT mice and non-transgenic controls. TERT mRNA was induced in a doxycycline-dependent manner in both MEFs and splenocyte cultures (Fig. S1a). Analysis of metaphase preparations ...
Physiological and Molecular Plant Pathology (2001) 59, 33-43
Physiological and Molecular Plant Pathology (2001) 59, 33-43

... (accession No: AF126402). The amino-acid sequences of AP1 and AP4 share 94 and 93 % identities, respectively, with that of a Mal d 1 isoform (accession No Z724251) from M. domestica cv. Gala [18], but only 76-77 % identities with the above-mentioned isoforms from the Golden Delicious cv. The tree [F ...
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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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