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Toxicity Mechanisms Identification via Gene Set
Toxicity Mechanisms Identification via Gene Set

... Toxicogenomics Time Series Data Generation. A highthroughput toxicogenomics assay was employed using the GFPfused stress response ensemble whole-cell library of E. coli K12, MG1655,23,24 with each fusion expressed from a low-copy plasmid, pUA66, which contains a kanamycin resistance gene and a fast ...
Genetic testing for asthma REVIEW
Genetic testing for asthma REVIEW

... Genetic testing for asthma G.H. Koppelman*, G.J. te Meerman# and D.S. Postma" ...
The Role of Mismatch Repair in Bacterial Evolution
The Role of Mismatch Repair in Bacterial Evolution

... mutS alleles and their respective strains (35). This is a result of frequent recombinational exchanges leading to the replacement of MMR mutator genes by non-mutator ones. In general, the sequence mosaicism of MMR genes may be a hallmark of a mechanism for adaptive evolution that involves modulation ...
TNFα signals through specialized factories where responsive coding
TNFα signals through specialized factories where responsive coding

... specialized NF-KB factories. A second question revolves around the number of clusters and whether these represent the Cook or Fraser type of "tx factory" or something else. Whereas the authors show colocalization of their target genes with p65 IF stained foci, they do not directly address whether th ...
evolution - Janelia Research Campus
evolution - Janelia Research Campus

... will use the two-dimensional case. Imagine that the phenotype currently sits on the edge of a circle; any position inside the circle represents an increased fitness and the center of the circle represents the optimal phenotype. A random change will then increase fitness less than half the time. For ...
Full Text  - Genes | Genomes | Genetics
Full Text - Genes | Genomes | Genetics

... only possible in a more aggregated form (for example at the level of protein complexes) (Mohr et al. 2014). We and others have recently developed a standardized RNAi based strategy, termed in vivo GFP interference (iGFPi) (or tag-mediated loss-of-function) (PastorPareja and Xu 2011; Neumuller et al. ...
Chapter 8 Using Dermatoglyphics from Down Syndrome and Class
Chapter 8 Using Dermatoglyphics from Down Syndrome and Class

... due to the degree of shared genetic heritage. Detecting positive correlations among relatives is a common approach for analyzing the genetic component of complex phenotypic traits. With this method it is very difficult, if not impossible, to determine the number of contributing genes. It is usually ...
Modeling of gene regulatory networks: A review
Modeling of gene regulatory networks: A review

... network is a fundamental problem in biology. With the availability of gene expression data and complete genome sequences, several novel experimental and computational approaches have recently been developed which helps to comprehensively characterize these regulatory networks by enabling the identif ...
SUNLIBB Work Packages, Aims and Achievements
SUNLIBB Work Packages, Aims and Achievements

... The aim of WP2 is to generate transcriptomic data for genes involved in secondary cell wall biosynthesis in maize, miscanthus and sugarcane. A better understanding of cell wall biosynthesis will allow the tailoring of lignocellulosic biomass for more efficient conversion into Biobased products. For ...
GA_lecture
GA_lecture

... In this case the goal was to evolve a structure with the size of 10 Lego units in each x-y-z dimension with the minimal weight. • Left structure was created at 895 generation and has sizes 10 by 10 by ...
−Table of Contents
−Table of Contents

... An identification of the unknown band 1 area was attempted using the uv-vis spectrum obtained. The unknown spectrum did not match up well with that of chalcone because it contained a peak around 270nm that chalcone lacks. The peaks of the unknown at 270nm and 362nm suggest that the unknown is a flav ...
Foundations of Biology - Geoscience Research Institute
Foundations of Biology - Geoscience Research Institute

... Down’s Syndrome)  Men have only one X chromosome and they are normal (at least they think so)  Women have two X chromosomes and they are normal  Mary Lyon proposed that the extra dosage of X chromosome that women have is compensated for by turning off one of the X chromosomes.  This turned-off c ...
Case report Homozygous Tangier disease with undetectable serum
Case report Homozygous Tangier disease with undetectable serum

... Tangier disease is caused by mutations in the ABCA1 gene which encodes the membrane transporter ABCA13. The ABCA1 gene resides on chromosome 9q22-q31, contains 50 exons, and codes for a 2261-amino acid long membrane protein4. In this case, the mutation was found to be a true homozygote for mutation ...
Solid Tumour Section Lung: non-small cell carcinoma with inv(2)(p21p23)
Solid Tumour Section Lung: non-small cell carcinoma with inv(2)(p21p23)

... Online updated version : http://AtlasGeneticsOncology.org/Tumors/inv2p21p23NSCCLungID5667.html DOI: 10.4267/2042/44570 This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 2.0 France Licence. © 2009 Atlas of Genetics and Cytogenetics in Oncology and Haematolog ...
PDF - WashU Epigenome Browser
PDF - WashU Epigenome Browser

... SNP and LD annotation tracks are available for human genomes. By default, the LD scoring system is D’. The correlation coefficient (R square) or LOD can be displayed using the configuration menu. These tracks can be found in the “Population variation” group of the annotation track panel. To search f ...
Van de Mark, Daniel: The Numerous Caveats of Designing, Implementing, and Interpreting Genome-Wide Association Studies
Van de Mark, Daniel: The Numerous Caveats of Designing, Implementing, and Interpreting Genome-Wide Association Studies

... here on, I will discuss only linking to disease phenotypes, but it is implied that the same methods could always be used to link variants to other quantitative traits). These studies involve genotyping members of a population on the basis of genetic markers that are spread throughout the genome, and ...
1 Feline Hypertrophic Cardiomyopathy (HCM) Genetic Testing
1 Feline Hypertrophic Cardiomyopathy (HCM) Genetic Testing

... have HCM on an ultrasound exam should be eliminated from the breeding population. Cats with a positive HCM genetic test should be screened by ultrasound to determine disease status and this overall information used in breeding decisions. Other health, type, and behavioral attributes should certainly ...
Bio 115 Lab 7: Probability and Genetics
Bio 115 Lab 7: Probability and Genetics

... The phenotype of an organism (the way it looks or behaves, or its physiology) is in large part determined by the genes it carries (its genotype). Most organisms are diploid, so that most carry two copies of each chromosome (a homologous pair). One chromosome of a homologous pair comes from the mothe ...
Document
Document

... Susskind and colleagues used bacteria with the chromosome illustrated (in smalr part) at bottom. The chromosome included two prophages: (1) a P22 prophage with a kanamycin resistance gene (yellow) driven by a λ PRM promoter with adjacent λ OR; (2) a λ prophage containing the λ cI gene (light green) ...
Question paper - Unit F215 - Control, genomes and
Question paper - Unit F215 - Control, genomes and

... (c) One effect of thyroid hormones is to increase the activity of mitochondria within cells. Suggest how the metabolism of a person with the condition congenital hypothyroidism might differ from that of a person who does not have this condition. ...
Variation in Drosophila melanogaster central metabolic genes
Variation in Drosophila melanogaster central metabolic genes

... of the method was evaluated by comparing the estimated frequency of each SNP after pyrosequencing to the expected frequency for the DGRP population based on the genome sequences (r ¼ 0.99). Pyrosequencing was carried out using PyroMark MD and peak heights scored to estimate SNP frequency. Primers we ...
Bio 211 Genetics Laboratory Experiment 5: Bioinformatics
Bio 211 Genetics Laboratory Experiment 5: Bioinformatics

... Exact match between the primer base and the corresponding base in the  matched sequence is indicated by a vertical line, while a mismatch does not  have this vertical line.  For example, find gb|AY258597.1| and you will note  that base position 43 of the forward primer does not match the DNA sequenc ...
Genotypes and phenotypes Review Proteomics and 2-DE
Genotypes and phenotypes Review Proteomics and 2-DE

... This leads us into a dilemma if we try to determine the precise and specific functions of a particular gene. The function of a gene is reflected by its phene. But where is the place on the long road from the genes to the external traits of an organism that most directly and specifically reveals the ...
Problem set 6 answers 1. You find a mouse with no tail. In order to
Problem set 6 answers 1. You find a mouse with no tail. In order to

... You then mate all the F1 males to their sisters and observe that three out of 42 F2 animals have no tail and two have short tails. What could explain this pattern of inheritance? There should be 1/4 m/m progeny from this cross, so many of these animals are wild type. The mutation results in a partia ...
Biology Ch. 12
Biology Ch. 12

... A. by activating genes to produce proteins that can overcome the disease B. by interfering with DNA replication in cells affected by the disease C. by preventing the translation of mRNA into the genes associated with the disease D. by shutting down protein synthesis in the cells of diseased tissues ...
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Genome (book)

Genome: The Autobiography of a Species in 23 Chapters is a 1999 popular science book by Matt Ridley, published by Fourth Estate.
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