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Lack of Association in Caucasians and African
Lack of Association in Caucasians and African

... 4 were calculated with respect to the null hypotheses that the corresponding ORs equal 1; they were derived using 2 X 2 contingency table statistics with Yate's continuity correction (29). ...
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... majority of phenotypic variation between these two species[1]. Moreover, it has long been speculated that mutations in gene regulatory elements (GREs) have a significant impact on evolution[2,3]. Since then, various lines of evidence have confirmed the functional impact of gene regulatory mutations[ ...
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... Note, however, this approximation works well only for small distances (d < 30 cM) but progressively fails at longer distances. This is because as the two loci get farther apart the RF reaches a maximum at 50%, like it would for two loci assorting independently (not linked). In fact, most chromosomes ...
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Glassman, S.

... pressure of the BM1 inversion in one X. the combination of heterozygous inversions in the presence of a free Y causes a high frequency of non-disjunction of the X’s, with resultant matroclinous daughters, bearing both the mother’s X’s, that can be scored for visible mutations arising in the original ...
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...  Is it reasonable to assume that the Q and q alleles will be alternatively “fixed” in the alternate F0 lines? Hence, that the QTL genotype of all F1 animals is the same? Especially when this is not the case for the SNP or microsatellite markers.  This has lead to many erroneous conclusions of impr ...
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... lutely necessary for germline divisions themselves, but are involved in a process that confers regularity to these divisions. In two of the loci (stall and pep) ovarian tumors are formed. These ovaries show ovarioles which contain many small, undifferentiated cells. A similar phenotype has been desc ...
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Genetic analysis of metabolites in apple fruits indicates an mQTL

... and LG16, were found to contain mQTL hotspots, mainly regulating metabolites that belong to the phenylpropanoid pathway. The genetics of annotated metabolites was studied in more detail using MapQTL. A number of quercetin conjugates had mQTLs on LG1 or LG13. The most important mQTL hotspot with the ...
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Chpt9_Transposition.doc
Chpt9_Transposition.doc

... resulting corn kernel will show the phenotypes specified by the dominant alleles. However, if the chromosome with the dominant alleles also has a Ds element, and Ac is present in the genome, the chromosome will break in some of the cells making up the kernel as some stage in development. Then the re ...
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Crossing Over…Markov Meets Mendel

... one of these two alleles. 2. Independent assortment: Alleles of different genes are inherited independently (later deemed not so accurate). The state of a gene, the genotype, is determined by the two alleles. The resulting trait, the phenotype, is then a function of this state. When the alleles are ...
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Commentary: Genotype does not determine phenotype

... there is no evidence for this view. Certainly in such populations the “static” transitions between the genotypical differences manifesting themselves in several characters may be called continuous—but such a “continuity of museums,” as it might be called, is not at all identical with genetic continu ...
GENETIC MODELS FOR DEVELOPMENTAL HOMEOSTASIS
GENETIC MODELS FOR DEVELOPMENTAL HOMEOSTASIS

... inversions in Drosophila pseudoobscura, Dobzhansky reached the conclusion that the frequency of inversion polymorphism in this species is under the control of natural selection, with individuals heterozygous for these inversions having a higher Darwinian fitness than either homozygote (Dobzhansky 19 ...
Effects of OPRM1, ABCB1 and CYP2D6 single nucleotide
Effects of OPRM1, ABCB1 and CYP2D6 single nucleotide

... R: 5’-GAAGAGAGACTlACATTAGGC-3’ encodes P-gp, an effCYP2D6*10 F: 5’-TCAACACAGCAGGTTCA-3’ 52°C 45 s ...
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Dominance (genetics)



Dominance in genetics is a relationship between alleles of one gene, in which the effect on phenotype of one allele masks the contribution of a second allele at the same locus. The first allele is dominant and the second allele is recessive. For genes on an autosome (any chromosome other than a sex chromosome), the alleles and their associated traits are autosomal dominant or autosomal recessive. Dominance is a key concept in Mendelian inheritance and classical genetics. Often the dominant allele codes for a functional protein whereas the recessive allele does not.A classic example of dominance is the inheritance of seed shape, for example a pea shape in peas. Peas may be round, associated with allele R or wrinkled, associated with allele r. In this case, three combinations of alleles (genotypes) are possible: RR, Rr, and rr. The RR individuals have round peas and the rr individuals have wrinkled peas. In Rr individuals the R allele masks the presence of the r allele, so these individuals also have round peas. Thus, allele R is dominant to allele r, and allele r is recessive to allele R. This use of upper case letters for dominant alleles and lower caseones for recessive alleles is a widely followed convention.More generally, where a gene exists in two allelic versions (designated A and a), three combinations of alleles are possible: AA, Aa, and aa. If AA and aa individuals (homozygotes) show different forms of some trait (phenotypes), and Aa individuals (heterozygotes) show the same phenotype as AA individuals, then allele A is said to dominate or be dominant to or show dominance to allele a, and a is said to be recessive to A.Dominance is not inherent to an allele. It is a relationship between alleles; one allele can be dominant over a second allele, recessive to a third allele, and codominant to a fourth. Also, an allele may be dominant for a particular aspect of phenotype but not for other aspects influenced by the same gene. Dominance differs from epistasis, a relationship in which an allele of one gene affects the expression of another allele at a different gene.
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