Apolipoprotein A5, a Newly Identified Gene That Affects Plasma
... A unique feature of APOA5 compared with its evolutionarily related apolipoprotein paralogues is its multiple transcripts of ⬇1.3 and 1.9 kb, as determined by Northern blot analysis.8 Alternative transcripts have not been described for other members within this gene cluster. Examination of expressed ...
... A unique feature of APOA5 compared with its evolutionarily related apolipoprotein paralogues is its multiple transcripts of ⬇1.3 and 1.9 kb, as determined by Northern blot analysis.8 Alternative transcripts have not been described for other members within this gene cluster. Examination of expressed ...
Document
... Quantification of the effect of promoter regions on reporter gene expression in transient assays can be used to gain information about how a particular section of DNA drives gene expression in isolation from a chromosomal context. There are advantages and disadvantages associated with using transien ...
... Quantification of the effect of promoter regions on reporter gene expression in transient assays can be used to gain information about how a particular section of DNA drives gene expression in isolation from a chromosomal context. There are advantages and disadvantages associated with using transien ...
Early Ideas of Heredity
... than one effect on the phenotype Seen in human diseases such as 1) cystic fibrosis 2) sickle cell anemia Multiple symptoms traced back to one defective allele ...
... than one effect on the phenotype Seen in human diseases such as 1) cystic fibrosis 2) sickle cell anemia Multiple symptoms traced back to one defective allele ...
Document
... genes involved in fatty acid metabolism of E. coli; under anaerobic conditions, transcription of fad regulon genes is increased upon the inactivation of ArcA, whereas, under aerobic conditions, transcription of those genes is not affected by the inactivation of ArcA; the fadR deletion affects both a ...
... genes involved in fatty acid metabolism of E. coli; under anaerobic conditions, transcription of fad regulon genes is increased upon the inactivation of ArcA, whereas, under aerobic conditions, transcription of those genes is not affected by the inactivation of ArcA; the fadR deletion affects both a ...
Evolutionary Computation - University of Kent School of computing
... A7 A2 0 A7 A5 0 0 represents a candidate solution where the attributes A7, A2 and A5 are selected. This unconventional individual encoding has some advantages, e.g. the fact that occurrences of very relevant attributes may be replicated across the genome. Regardless of the internal details of indiv ...
... A7 A2 0 A7 A5 0 0 represents a candidate solution where the attributes A7, A2 and A5 are selected. This unconventional individual encoding has some advantages, e.g. the fact that occurrences of very relevant attributes may be replicated across the genome. Regardless of the internal details of indiv ...
... β-tubulin gene specific primers were obtained from Genei, Bangalore. These were used to amplify βtubulin gene from the genomic DNA of each mutant along with the wild strain. PCR reaction was set up under sterile conditions in 200 µl capacity PCR tubes. The PCR mixture contained 200 ng of template DN ...
Apolipoprotein A5, a Newly Identified Gene That Affects Plasma
... A unique feature of APOA5 compared with its evolutionarily related apolipoprotein paralogues is its multiple transcripts of ⬇1.3 and 1.9 kb, as determined by Northern blot analysis.8 Alternative transcripts have not been described for other members within this gene cluster. Examination of expressed ...
... A unique feature of APOA5 compared with its evolutionarily related apolipoprotein paralogues is its multiple transcripts of ⬇1.3 and 1.9 kb, as determined by Northern blot analysis.8 Alternative transcripts have not been described for other members within this gene cluster. Examination of expressed ...
Missense mutation in the ligand-binding domain of the horse
... The qPCR revealed signals from all 5 Y-chromosomal genes (SRY, ZFY, EIF1AY, TSPY, and USP9Y) in HT, DSD, the control stallion and also identified XY chromosome constitution in one half-sister (CM14). This animal was a previously unidentified case of XY DSD. The X-chromosomal qPCR signal was observed ...
... The qPCR revealed signals from all 5 Y-chromosomal genes (SRY, ZFY, EIF1AY, TSPY, and USP9Y) in HT, DSD, the control stallion and also identified XY chromosome constitution in one half-sister (CM14). This animal was a previously unidentified case of XY DSD. The X-chromosomal qPCR signal was observed ...
PDF - Oxford Academic - Oxford University Press
... The longevity phenotype measures overall life span without consideration of health and physical or cognitive function and hence is a very heterogeneous phenotype that may be affected by many environmental and other nongenetic factors. The relative contribution of additive genetic effects may be grea ...
... The longevity phenotype measures overall life span without consideration of health and physical or cognitive function and hence is a very heterogeneous phenotype that may be affected by many environmental and other nongenetic factors. The relative contribution of additive genetic effects may be grea ...
Association genetics of complex traits in conifers
... identified in tomatoes and maize [8,9]. Species of the forest tree genus Populus also possess many of these attributes but, as yet, QTLs have not been positionally cloned in these species. By contrast, it is not possible to clone QTLs positionally in conifers. Genome sizes are large [10], there are ...
... identified in tomatoes and maize [8,9]. Species of the forest tree genus Populus also possess many of these attributes but, as yet, QTLs have not been positionally cloned in these species. By contrast, it is not possible to clone QTLs positionally in conifers. Genome sizes are large [10], there are ...
Introduction to Genetics - Bruce Walsh's Home Page
... Each parent contributes one of its two alleles (at random) to its offspring Hence, a YY parent always contributes a Y, while a gg parent always contributes a g An individual carrying only one type of an allele (e.g. yy or gg) is said to be a homozygote In the F1, YY x gg --> all individuals are Yg ...
... Each parent contributes one of its two alleles (at random) to its offspring Hence, a YY parent always contributes a Y, while a gg parent always contributes a g An individual carrying only one type of an allele (e.g. yy or gg) is said to be a homozygote In the F1, YY x gg --> all individuals are Yg ...
Commonly Used STR Markers
... Must agree how to name and genotype STRs so that matches can be made • Name is based on core repeat unit: – Example – AGAT ...
... Must agree how to name and genotype STRs so that matches can be made • Name is based on core repeat unit: – Example – AGAT ...
Goldmine: Integrating information to place sets of genomic ranges
... the goldmine() function. The data source for the gene and feature sets is the table archive of the UCSC Genome Browser. The first time a table is needed, Goldmine will download and cache the table. On subsequent calls to goldmine(), and other functions that access UCSC Genome Browser tables, the dat ...
... the goldmine() function. The data source for the gene and feature sets is the table archive of the UCSC Genome Browser. The first time a table is needed, Goldmine will download and cache the table. On subsequent calls to goldmine(), and other functions that access UCSC Genome Browser tables, the dat ...
Gene Section SSX2 (synovial sarcoma, X breakpoint 2) in Oncology and Haematology
... variants are rare. One was described by Fligman et al (1995). It contains an additional 126 bp segment proximal to SSX2 Exon 6, where the break occurred in Exon 5 while maintaining the frame. Another SS18-SSX2 variant includes 50 additional base pairs of SSX2 Exon 5 (Otsuka et al., 2006). Hybrid/Mut ...
... variants are rare. One was described by Fligman et al (1995). It contains an additional 126 bp segment proximal to SSX2 Exon 6, where the break occurred in Exon 5 while maintaining the frame. Another SS18-SSX2 variant includes 50 additional base pairs of SSX2 Exon 5 (Otsuka et al., 2006). Hybrid/Mut ...
How to complete a Test Cross
... Explain how TWO factors lead to variation. Must include the idea of inheritance. Eg Mutation – change in the genetic makeup. If this change occurs in the somatic cells, it cannot be passed on, but if in the sex cell, it may be inherited. Meiosis – each parent passes on one member of each pair of hom ...
... Explain how TWO factors lead to variation. Must include the idea of inheritance. Eg Mutation – change in the genetic makeup. If this change occurs in the somatic cells, it cannot be passed on, but if in the sex cell, it may be inherited. Meiosis – each parent passes on one member of each pair of hom ...
1 - KSU Faculty Member websites
... occurs during prophase. B. occurs during anaphase. C. occurs during interphase. D. occurs during all stages of meiosis. Answer:C ...
... occurs during prophase. B. occurs during anaphase. C. occurs during interphase. D. occurs during all stages of meiosis. Answer:C ...
CFTR: The Gene Associated with Cystic Fibrosis Official Gene
... normal, functional copy of the CFTR gene and one mutated copy would just be a carrier of the disorder, and would not display typical CF symptoms. It is important to note that just because two people might have the same two copies of the mutated CFTR gene, each may experience very different symptoms. ...
... normal, functional copy of the CFTR gene and one mutated copy would just be a carrier of the disorder, and would not display typical CF symptoms. It is important to note that just because two people might have the same two copies of the mutated CFTR gene, each may experience very different symptoms. ...
Cancer Prone Disease Section X-linked lymphoproliferative disease (XLP) in Oncology and Haematology
... XLP1 or -2 patient who experiences primary EBV infection. Lymphomas can be effectively treated with standard chemotherpateutic regimens; however, patients should be carefully monitored for the development of EBV and other infections, which can be difficult to manage due to underlying immune defects. ...
... XLP1 or -2 patient who experiences primary EBV infection. Lymphomas can be effectively treated with standard chemotherpateutic regimens; however, patients should be carefully monitored for the development of EBV and other infections, which can be difficult to manage due to underlying immune defects. ...
Correlated selection responses in animal domestication: chickens
... pressures; selection for production traits is introduced, and animals are faced with larger and denser social groups. It is not unexpected then that domestication produces a simultaneous change in a number of traits, both physiological and behavioural. This correlated change in traits, e.g. egg prod ...
... pressures; selection for production traits is introduced, and animals are faced with larger and denser social groups. It is not unexpected then that domestication produces a simultaneous change in a number of traits, both physiological and behavioural. This correlated change in traits, e.g. egg prod ...
Recombinant DNA Technology
... scientists can alter DNA, they can then insert desired genes into another organism. They can alter the genes of bacteria to cause them to produce a desired human protein product. 2. Once a gene is sequenced, it can be used in recombinant DNA techniques. Sequencing is a technique used to determine th ...
... scientists can alter DNA, they can then insert desired genes into another organism. They can alter the genes of bacteria to cause them to produce a desired human protein product. 2. Once a gene is sequenced, it can be used in recombinant DNA techniques. Sequencing is a technique used to determine th ...
MUTATIONS
... FRAMESHIFT MUTATION A frameshift mutation changes the amino acid sequence from the site of the mutation. ...
... FRAMESHIFT MUTATION A frameshift mutation changes the amino acid sequence from the site of the mutation. ...
Has the combination of genetic and fossil evidence solved the riddle
... Polygenic trait—a trait that is influenced in its expression by differences in the alleles that individuals have at several or many different genetic loci. Quantitative trait linkage analysis—any of a related series of statistical techniques that search for correlation between variants at many loci i ...
... Polygenic trait—a trait that is influenced in its expression by differences in the alleles that individuals have at several or many different genetic loci. Quantitative trait linkage analysis—any of a related series of statistical techniques that search for correlation between variants at many loci i ...
Masters_Thesis_Final - JScholarship
... (courtesy of Dr. Dan Arking). Additional common SNPs were obtained from the 1000 Genomes project. ...
... (courtesy of Dr. Dan Arking). Additional common SNPs were obtained from the 1000 Genomes project. ...
Male Sex Drive and the Maintenance of Sex
... among the 12 species examined, indicating either that these genes are so diverged that orthology cannot be unambiguously assigned or that there is an overrepresentation of lineage-specific, de novo genes among those with male function (Haerty et al. 2007; see below). In addition to their rapid evolu ...
... among the 12 species examined, indicating either that these genes are so diverged that orthology cannot be unambiguously assigned or that there is an overrepresentation of lineage-specific, de novo genes among those with male function (Haerty et al. 2007; see below). In addition to their rapid evolu ...