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Nematode genome evolution
Nematode genome evolution

... 3. The evolution of chromosome number and structure 3.1. The range of haploid chromosome numbers among nematodes Most nematodes have haploid chromosome numbers of n=4–12 (Walton, 1959). The karyotypes of just ~300 species have been studied, but nematodes display a lot of karyotypic variation (Špakul ...
Mutations in the gene encoding methyl-CpG-binding
Mutations in the gene encoding methyl-CpG-binding

... has either the wild-type or the mutant MECP2active. This excludes a possible dominant-negative mechanism in which the protein produced from the mutant allele would interfere with the function of its wild-type counterpart. However, it does not exclude the less likely alternative of dominant– negative ...
The common bean growth habit gene PvTFL1y is a
The common bean growth habit gene PvTFL1y is a

... Using the sequences obtained with degenerate primers (Kwak et al. 2008), the BD GenomeWalkerTM Universal Kit (BD Biosciences Clontech, Mountain View, CA, USA) was used to extend sequences of PvTFL1y using the method recommended by the manufacturer. The genomic libraries of G12873 and Midas were cons ...
Genetics of Indo-European populations: the past, the future*
Genetics of Indo-European populations: the past, the future*

... Without a doubt, coinciding results of linguistic and genetic studies could tell even more about population history; finding such examples is always pleasant for researchers. Our study on North Caucasian populations [Balanovsky et al., 2011] provided the best fit published to date. We studied the Y­ ...
Gene Section SSX2 (synovial sarcoma, X breakpoint 2) in Oncology and Haematology
Gene Section SSX2 (synovial sarcoma, X breakpoint 2) in Oncology and Haematology

I. Mitosis - MSU Billings
I. Mitosis - MSU Billings

... 22. Between the two divisions of meiosis there is A. a full cell cycle. B. a pairing of homologues. C. replication of some parts of the chromosomes. D. no S phase. E. random combination among chromatids. 23. Crossing over of chromosomes takes place in A. prophase II. B. prophase I. C. interphase II. ...
application of next generation sequencing in the diagnosis
application of next generation sequencing in the diagnosis

... case of FBH, the mode of inheritance is autosomal dominant, and this disease is caused by a single heterozygous mutation either in COL4A3 or in COL4A4 genes 10. If there are two mutations either in COL4A3 or COL4A4 genes,—a more severe— form of AS develops. Because of this FBH can be viewed as the c ...
Evolutionary Origin and Adaptive Function of Meiosis
Evolutionary Origin and Adaptive Function of Meiosis

... ordinary molecular subunits that are not endowed with any unusual quantum mechanical stability, and this “chemical vulgarity” makes DNA vulnerable to all the “chemical horrors” that might befall any such molecule in a warm aqueous environment. The particular types of DNA damage occurring when organi ...
! Mendel`s Law of Independent Assortment
! Mendel`s Law of Independent Assortment

... see that each of these is ¼ of the total number of squares. How do we get the phenotypic results? The sum rule of probability tells us that when the same event can occur in more than one way, we can add the results. Because 1, 2, and 3 all result in unattached earlobes, we add them up to know that t ...
Template for Exome Report Abstract. The abstract should include
Template for Exome Report Abstract. The abstract should include

... The declaration is made using this DECIPHER xls file provided. All items, including those that are not mandatory for DECIPHER, must be completed, according to DECIPHER keywords. The main phenotypic traits must be added using HPO. 5.2. Subset of variations reported in the manuscript Among variants, ...
NIH Public Access
NIH Public Access

... that have a given connectivity.(34) Degree distribution is calculated by counting the number of nodes of a given k and dividing by the total number of nodes.(34) The topology of a network can be revealed by plotting the degree distribution P(k). In a random network, this plot results in a bell curve ...
Genetic polymorphisms in biotransformation enzymes in
Genetic polymorphisms in biotransformation enzymes in

... aetiology of Crohn’s disease. Biotransformation enzymes play a pivotal role in a variety of detoxification processes. In this case control study, we found a highly significant difference in allele frequency of the Tyr113 variant in exon 3 of the EPXH gene between patients with Crohn’s disease (0.67) ...
Evolutionary relationships and diversification of barhl genes within
Evolutionary relationships and diversification of barhl genes within

... although few cells co-expressing both genes are always visible at the expression boundaries (as indicated by arrows in Figure 4D-E, and 4N-O). Therefore, in contrast with barhl1.2, the complementary expression of barhl2 and atoh7 suggests a reciprocal negative regulation between these two genes. To ...
Lesson 3: Can you taste PTC?
Lesson 3: Can you taste PTC?

... otypes and their phenotypes are not always 100%, as in the case of polygenic phenotypes or in‐ complete penetrance)?    4)  Ask student pairs to determine how they would test the rela onship between TAS2R38 genotype  and PTC phenotype among their fellow students.  What data would they collect?  How  ...
Variations in the Expression of Genetic Myths Among Twins
Variations in the Expression of Genetic Myths Among Twins

... There are a list of characters like arm folding, clasping of hands, hitchhiker’s thumb, bent pinkie,darwin’s tubercle, lengthier 2nd toe, type of ear wax, attached ear lobe, cheek and chin dimple,mid-digital hair, tongue rolling etc which are called genetic myths but are proven mostly not to have a ...
In Vitro Cell. Dev. Biol. In Press
In Vitro Cell. Dev. Biol. In Press

... DNA (10 mg) was digested with HindIII and fractionated on a 0.8% agarose gel and blotted onto a nylon membrane (Genescreenplus, Dupont). A 0.6 kb fragment encompassing npt II sequence from the plasmid pME 504 was labeled with [a-32P]dCTP using a random primer labeling kit (Amersham Biosciences) and ...
Adaptive Evolution of 5#HoxD Genes in the
Adaptive Evolution of 5#HoxD Genes in the

... First, the divergence of the early cetaceans from their even-toed relatives coincided with the reacquisition of the pentadactyl forelimb, whereas the ancestors of tetradactyl baleen whales (Mysticeti) later lost a digit again. To test whether the evolution of the cetacean forelimb is associated with ...
Evaluation of genomic DNA from paraffin
Evaluation of genomic DNA from paraffin

... The Newfoundland breed has an increased incidence for DCM (Tidholm & Jönsson 1997) and shows attenuated wavy fibers (Tidholm et al. 1998). Even seven of 15 examined Newfoundland dogs without any abnormalities in echocardiographical examination or clinical signs for heart disease have been reported t ...
Basic Genetics for the Cat Breeder
Basic Genetics for the Cat Breeder

... color is represented (either black or red) but in the female who has two X chromosomes, it is possible that both black and red can be expressed – tortoiseshell. ...
Gene Section MAP2K4 (mitogen activated protein kinase kinase 4) -
Gene Section MAP2K4 (mitogen activated protein kinase kinase 4) -

Genetics-HEREDITY Unit Overview
Genetics-HEREDITY Unit Overview

... 4. Chromosome - Long pieces of DNA found in the center (nucleus) of eukaryotic cells 5. Co-dominance____________________________________________________________ ______________________________________________________________________ 6. Cross ___________________________________________________________ ...
www.LessonPlansInc.com
www.LessonPlansInc.com

... Standards: CA Biology 5c Students know how mutations in the DNA sequence of a gene may or may not affect the expression of the gene or the sequence of amino acids in an encoded protein. 5e Students know proteins can differ from one another in the number and sequence of amino acids. 7a Students know ...
With the inclusion of incomplete dominance
With the inclusion of incomplete dominance

... gene. We now know that this is an oversimplification. Although individual humans (and alldiploid organisms) can only have two alleles for a given gene, multiple alleles may exist at the population level such that many combinations of two alleles are observed. Note that when many alleles exist for th ...
Replication studies in longevity: puzzling findings in Danish
Replication studies in longevity: puzzling findings in Danish

... pool (Table 2). These results may be caused by a different recruitment of Danish and Italian samples, or occur by chance. However, it is worth noting that a similar phenomenon was observed for the Tyrosine Hydroxylase (TH) gene, whose HUMTHO–STR marker was found to be positively associated with long ...
Host-Plasmid Interactions in Saccharomyces
Host-Plasmid Interactions in Saccharomyces

... After transformation of each of these two plasmids into the n, 2n and 4n strains, the stability of the plasmids following transfer from selective to non-selective growth conditions was examined in two ways: (a) by calculating the rate of plasmid loss per cell division (i) during exponential growth; ...
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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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