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The Complex Inheritance of Maize Domestication Traits and Gene
The Complex Inheritance of Maize Domestication Traits and Gene

... I want to extend my thanks to John Doebley for making this dissertation possible. John has been a constant voice of encouragement and insight throughout my graduate career. He has been instrumental in keeping me focused on the big question, while allowing me the freedom to chase down side interests ...
Practice Genetic Problems PMB 220 1. In working with a haploid
Practice Genetic Problems PMB 220 1. In working with a haploid

... spores and 20 of these were isolated at random. When the resulting cultures were tested on various media, they give the results shown below, were Arg means arginine is added to the medium, Ad, means adenine is added to the medium, Nic means nicotinamide is added to the medium and Leu means leucine i ...
C57BL/6 - Envigo
C57BL/6 - Envigo

How to recognize and diagnose chromosome rearrangements. David D. Perkins Background
How to recognize and diagnose chromosome rearrangements. David D. Perkins Background

... identify and score genes that confer vegetative incompatibility). At least a few ascospores can be obtained from heterozygous crosses of most duplications. As expected, these produce black ascospores, some of which are duplications. Deficiencies. Meiotic products carrying a segmental deficiency can ...
1999 Dekkers: BREEDING IN THE 21st CENTURY
1999 Dekkers: BREEDING IN THE 21st CENTURY

... collective effect of polygenes. Kennedy et al (1992) suggested inclusion of genotype as a fixed effect in an animal model to estimate the effects of known genes, capitalizing on population-wide disequilibrium. Fernando and Grossman (1989) developed BLUP-QTL models for QTL linked to markers, relying ...
Variability of polyphenol oxidase (PPO) alleles located on
Variability of polyphenol oxidase (PPO) alleles located on

... its interaction with PPO genes, we found that 50% of the PPO activity was determined by the variations in allelic genes on chromosomes 2A and 2D, whereas 37–50% of the activity was controlled by genetic background and 9% by the interaction between genetic background and PPO genes. This result sugges ...
Expression and characterization of von Willebrand
Expression and characterization of von Willebrand

... subtypes IIA, IIC, IID, IIE, IIF, IIG, and IIH, have been combined to form a common type, vWD type 2A, which comprises all variants lacking HMWM in plasma.11 The single exception is type 2B, in which the absence of plasma HMWM ...
Functional Interactions of Genes Mediating Convergent Extension
Functional Interactions of Genes Mediating Convergent Extension

Derivative Alleles of the Arabidopsis Gibberellin
Derivative Alleles of the Arabidopsis Gibberellin

... has an important role in floral initiation in short photoperiods (Wilson et al., 1992). gai is a mutation conferring insensitivity to GA (Koornneef et al., 1985a). Plants containing gai resemble plants homozygous for mutations at the GA7 to GA5 loci; they are dwarfed, darker green, and display reduc ...
Hox patterning of the vertebrate axial skeleton
Hox patterning of the vertebrate axial skeleton

... Together, these experiments provided strong evidence that the HomC genes are critical AP patterning cues in the development of the body plan in Drosophila. In single Hox mutant mice, however, some defects have been characterized as anterior homeotic transformations—the kinds of transformations that ...
American Thoracic Society Documents
American Thoracic Society Documents

... 2. To improve general knowledge regarding PHOX2B as the disease-defining gene for CCHS. The reader will learn that (i) approximately 90% of individuals with the CCHS phenotype are heterozygous for a polyalanine expansion repeat mutation in the PHOX2B gene, (ii) approximately 10% of individuals with ...
11.1-11.3 Notes
11.1-11.3 Notes

... passed from one parental generation to the next. ...
A role for wingless in the segmental gradient of Drosophila?
A role for wingless in the segmental gradient of Drosophila?

... for 2.5 hours at 25°C, then aged 13.5 hours at 15°C, given a heatshock pulse and left at 15°C for 4 days. Although the resulting smooth phenotypes are more variable than those of embryos kept at 15°C all the time, we did not observe consistent differences between embryos with or without the HSwg con ...
redundancy and regulatory interactions between two
redundancy and regulatory interactions between two

Daniël van Draanen - Utrecht University Repository
Daniël van Draanen - Utrecht University Repository

org.Mm.eg.db
org.Mm.eg.db

Jaw and branchial arch mutants in zebrafish I: branchial
Jaw and branchial arch mutants in zebrafish I: branchial

... flathead group, lack several adjacent branchial arches and their associated cartilages. Five alleles at the flathead locus all lead to larvae that lack arches 4-6. Among 34 other flathead group members complementation tests are incomplete, but at least six unique phenotypes can be distinguished. The ...
Mesenchymal Dysplasia: A Recessive Mutation
Mesenchymal Dysplasia: A Recessive Mutation

... pellet and ash weight yielded the amount of protein. These data were corrected for aliquot size to obtain the final absolute amounts of fat, protein, and mineral present in each carcass. The data are expressed as a percent of total carcass weight and were analyzed without arcsine transformation beca ...
Scriver Charles R. Garrod`s Croonian Lectures (1908)
Scriver Charles R. Garrod`s Croonian Lectures (1908)

... way, he studied disease and found particular forms of evidence from which he assembled the larger vision. During the past 100 years, the evidence garnered from the four inborn errors of metabolism, described in his Croonian Lectures, has grown and been refined. That legacy of the Croonian Lectures i ...
Lecture 4
Lecture 4

... Maternal Rescue Hide an essential role for a gene in embryonic pattern formation. Pure zygotic screens may miss important functions. ...
Help Me Understand Genetics
Help Me Understand Genetics

... DNA, or deoxyribonucleic acid, is the hereditary material in humans and almost all other organisms. Nearly every cell in a person’s body has the same DNA. Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where ...
oto`s role in head and trunk development
oto`s role in head and trunk development

... requirement that is consistent with other recent insights into the regulation of mammalian anterior development. The first obvious sign of anteroposterior (AP) pattern in the mouse embryo is provided by the formation of the primitive streak. Molecular studies have shown that AP pattern in the viscer ...
Genetics: Mendelian Genetics (1) Patterns of Inheritance
Genetics: Mendelian Genetics (1) Patterns of Inheritance

... the basis of a theory (Law) of segregation, which we state here in modern terms: ...
COAGULATION AND TRANSFUSION MEDICINE Original Article
COAGULATION AND TRANSFUSION MEDICINE Original Article

Hereditary ataxias: overview
Hereditary ataxias: overview

... each disorder see GeneReviews.org). Although ordering molecular testing for the polyglutamine ataxia disorders listed above is straightforward and tests are commercially available, there are two notes of caution in the interpretation of results: 1. Some disorders are associated with alleles for whi ...
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Epistasis



Epistasis is a phenomenon that consists of the effect of one gene being dependent on the presence of one or more 'modifier genes' (genetic background). Similarly, epistatic mutations have different effects in combination than individually. It was originally a concept from genetics but is now used in biochemistry, population genetics, computational biology and evolutionary biology. It arises due to interactions, either between genes, or within them leading to non-additive effects. Epistasis has a large influence on the shape of evolutionary landscapes which leads to profound consequences for evolution and evolvability of traits.
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