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Identification of Novel Non-Metal Haloperoxidases from the Marine
Identification of Novel Non-Metal Haloperoxidases from the Marine

... However, clones in group B, including CS19 HPO clone, showed relatively higher homology of approximately 80% with 70% identity as shown in Fig. 3. ...
Chapter 5 Gases - Saint Demetrios Astoria School
Chapter 5 Gases - Saint Demetrios Astoria School

... Number Changes in Humans? (cont’d.) – Trisomy 21 (Down syndrome) • A normal gamete (n) fuses with an n+1 gamete • New individual is trisomic (2n+1), having three of one type of chromosome and two of every other type • Effects: Mild to moderate mental impairment; health problems such as heart disease ...
Application of the new manP counter-selection system for B. subtilis
Application of the new manP counter-selection system for B. subtilis

... subtilis, iii) encodes an antibiotic resistance gene for selection in B. subtilis and iiii) ...
LacZ Reporter Gene Expression in 81 KOMP Heterozygous Mutants
LacZ Reporter Gene Expression in 81 KOMP Heterozygous Mutants

... sections has a similar anatomical distribution and is observed less frequently than that found with whole-mounts. ...
Journal of Genomics The Sex Chromosomes of Frogs: Variability
Journal of Genomics The Sex Chromosomes of Frogs: Variability

... to mammals, Drosophila have a macromolecular complex thought to increase expression of genes on the single male X chromosome by about 2-fold, thus making male and female expression effectively the same; it is worth noting, however, that complex network dynamics and transcriptional control are also i ...
HMW glutenin subunits in multiploid Aegilops species: composition
HMW glutenin subunits in multiploid Aegilops species: composition

... presence of the subunits possessing an electrophoretic mobility similar to, or larger than, that of the 1Dx2.2 subunit was observed. However, it was not known if these subunits were encoded by the D genome component in the relevant Aegilops species. ( ) Genomic PCR reactions. Based on the above SDS- ...
Conservation and diversification of gene function during mouthpart
Conservation and diversification of gene function during mouthpart

... The mandibles are the chewing mouthparts, articulated to the head by two condyles. From the base of the mandibles extend two lobes: the distal incisor lobe and the inner median molar lobe, which are linked by a flexible area (Fig. 5Ai to iv). The setae on the inner periphery of the incisor lobe delim ...
Genomic Analysis of Arabidopsis Thaliana
Genomic Analysis of Arabidopsis Thaliana

... many generations to select for increased utility as food and agricultural resources compared to wild-type progenitors. The selection of traits was intended for practical use, not for plant scientists. As a result, crops have a genetic bias for agricultural purposes, such as increased yield, growth, ...
A genome-wide association scan in pig identifies novel regions
A genome-wide association scan in pig identifies novel regions

... availability of the PorcineSNP60 BeadChip (Illumina, San Diego, CA), which contains more than 62,000 SNP spread over entire porcine genome, gives us the opportunity to carry out association studies to map chromosomal regions associated with economically important traits in pigs at the population lev ...
Multi-petal cyclamen flowers produced by
Multi-petal cyclamen flowers produced by

... although the transcripts of each gene were also detected in stamen, carpel and receptacle6. Chimeric repressor gene-silencing technology (CRES-T) provides a powerful tool for dominant negative genetic modification of a transcription factor. In CRES-T, a short but strong, plant-specific transcription ...
The relationship between higher‑order chromatin structure and
The relationship between higher‑order chromatin structure and

... sediments more slowly than bulk chromatin or a non‑expressed gene, whereas it sediments with bulk chromatin in non‑expressing cells [8,9,11]. However, can the β‑globin locus, whose regulation is known to be very complex in mammalian cells, be used as a paradigm for the other ∼25 000 genes in the gen ...
Deficiency in plastidic glutamine synthetase alters proline
Deficiency in plastidic glutamine synthetase alters proline

... by the action of arginase (Delauney et al., 1993). The importance of this alternative pathway for proline synthesis is controversial. In some plants, the arginase ⁄ OAT route seems to have an important role in stress-induced proline production (Xue et al., 2009 and references therein). However, anal ...
AnsteadSeniorHonorsThesis
AnsteadSeniorHonorsThesis

... located on the 2nd chromosome, with males having deficiency regions located on the 3rd chromosome, which span multiple genes. To measure the results, two genetic markers will be attached to the mutants with deficiencies: curly wings (compared to the wild-type straight wings), located on the second c ...
Genetic Evidence for a Silent SUC Gene in Yeast.
Genetic Evidence for a Silent SUC Gene in Yeast.

... and LAMPEN 1968; OTTOLENGHI1971). Six nonallelic SUC loci (SUCI-SUC6) were previously identified by segregational analysis of cliff erent Saccharomyces 1949; WINGEand ROBERTS1952; MORTIMER and strains (Table 1) (GILLILAND HAWTHORNE 1966). Any individual haploid strain of yeast may have zero, one, (1 ...
Correction to “Frequency of Undetected CYP2D6
Correction to “Frequency of Undetected CYP2D6

... The frequency of hybrids genes in CYP2D6*4 and CYP2D6*10 samples is reported for both heterozygous or homozygous and heterozygous alone. We did not determine whether one or both chromosomes contained a hybrid tandem in homozygous samples. For this reason, to determine the risk that a CYP2D6*4 or CYP ...
credits - CiteSeerX
credits - CiteSeerX

... saw that many traits existed in either of two possible forms. A pea plant was either tall or short; its seeds were either yellow or green. Mendel studied seven different traits that appeared in the pea plants. Obviously, Mendel knew nothing of genes, chromosomes, or the processes of mitosis and meio ...
GENETICS accepted
GENETICS accepted

... SNP analysis. him-5(ok1896) was introgressed into the Hawaiian CB4658 background by repeated backcrosses. Hawaiian specific alleles used in these studies were confirmed by PCR genotyping. Spontaneous males from this stock were crossed to dpy-17(e164); him-5(ok1896) and non-Dpy, him-5 trans-heterozyg ...
A Common Polygenic Basis for Quinine and
A Common Polygenic Basis for Quinine and

... differences result from allelic variation at a single locus. However, segregation patterns incompatible with monogenic inheritance have been found for quinine avoidance. The Soa bitter sensitivity locus exerts some influence on this phenotype, but an unknown number of other loci also contribute. Rel ...
View PDF - G3: Genes | Genomes | Genetics
View PDF - G3: Genes | Genomes | Genetics

... chromosome (t-test, P , 0.001). However, the numbers varied widely among crosses due to variable mating efficiency. A total of 72.5% and 52.4% of crosses produced a minimum of 50 and 100 deficiencycarrying females, respectively, summed over replicates. The percentage of each chromosome arm covered is ...
New functions of the Drosophila rhomboid gene
New functions of the Drosophila rhomboid gene

... varying degrees in the enhancer piracy line shown in Fig. 2FH. The most common defect is a loss of one or both halteres (Fig. 2F). Strongly affected individuals may also lack part of the wing, resulting in the formation of a mirror symmetric double anterior wing (Fig. 2G), or may lack virtually all ...
Restriction Fragment Length Polymorphism of hsp70
Restriction Fragment Length Polymorphism of hsp70

... Previous studies from our laboratory have demonstrated that the intermediate phenotype of thermosensitivity is present in hypertensive mice and rats. Increased expression of hsp70 caused by increased transcription rate was demonstrated in vivo, in organs, and in cultured cells from spontaneously hyp ...
PHI-Canto video tutorial text - PHI-base
PHI-Canto video tutorial text - PHI-base

Molecular genetics of Rett syndrome and clinical
Molecular genetics of Rett syndrome and clinical

... expression of a select group of genes, although the mechanism that might account for this is dif®cult to predict. These genes may be neuronal-speci®c or widely expressed but detrimental only to neuronal development when misexpressed. In support of the idea that MeCP2 might regulate only a subset of ...
Chapter 44 Self Test (EOC)
Chapter 44 Self Test (EOC)

... Answer— The latter view represents our current understanding. There are many examples of small gene families (such as, Hox, MADS) whose apparent role in generating phenotypic diversity among major groupings of organisms is in altering the expression of other genes. Alterations in timing (heterochron ...
Hox Targets and Cellular Functions
Hox Targets and Cellular Functions

... distinct cell affinities, regulate cell proliferation, and establish organ shape [40]. The identification of realizator genes was, therefore, key to understand how Hox genes shape different structures. Different approaches to isolate and characterize Hox targets in Drosophila and vertebrates were in ...
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Genomic imprinting

Genomic imprinting is the epigenetic phenomenon by which certain genes are expressed in a parent-of-origin-specific manner. If the allele inherited from the father is imprinted, it is thereby silenced, and only the allele from the mother is expressed. If the allele from the mother is imprinted, then only the allele from the father is expressed. Forms of genomic imprinting have been demonstrated in fungi, plants and animals. Genomic imprinting is a fairly rare phenomenon in mammals; most genes are not imprinted.In insects, imprinting affects entire chromosomes. In some insects the entire paternal genome is silenced in male offspring, and thus is involved in sex determination. The imprinting produces effects similar to the mechanisms in other insects that eliminate paternally inherited chromosomes in male offspring, including arrhenotoky.Genomic imprinting is an inheritance process independent of the classical Mendelian inheritance. It is an epigenetic process that involves DNA methylation and histone methylation without altering the genetic sequence. These epigenetic marks are established (""imprinted"") in the germline (sperm or egg cells) of the parents and are maintained through mitotic cell divisions in the somatic cells of an organism.Appropriate imprinting of certain genes is important for normal development. Human diseases involving genomic imprinting include Angelman syndrome and Prader–Willi syndrome.
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