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Exome Sequencing Project release
Exome Sequencing Project release

... population and often were only observed in a single individual, explained Dr. Leal, who presented the findings today at the American Society of Human Genetics 2012 meeting. Dr. Leal added that most of the observed coding variants are population specific, occurring in either European or African Ameri ...
A founder mutation of the potassium channel KCNQ1 in long
A founder mutation of the potassium channel KCNQ1 in long

... of symptomatic mutation carriers (470 ⫾ 30 ms) was significantly longer than that of the asymptomatic ones (450 ⫾ 30 ms, p ⬍ 0.001), and there was an increasing likelihood of occurrence of symptoms by increasing QTc value (Fig. 3). In 48 cases (58%) the triggering factor for syncope could unequivoca ...
A statistical framework for genome
A statistical framework for genome

... more consistent results across different studies. Fourth, it significantly facilitates the interpretation of the association findings by incorporating prior knowledge of biological pathways into association inference. A variety of statistical or computational methods have been developed to identify ...
Klug10chapt03
Klug10chapt03

... 3.4 The Trihybrid Cross Demonstrates That Mendel’s Principles Apply to Inheritance of Multiple Traits 3.4.1 The Forked-Line Method, or Branch Diagram ...
Ch. 9 Meiosis
Ch. 9 Meiosis

... Inheritable traits are carried on factors called genes and are passed down from generation to generation. ...
"Engineering Large Animal Species to Model Human Diseases". In
"Engineering Large Animal Species to Model Human Diseases". In

... (iPS) cells have also been developed for livestock species, and while there has been one report of germline transmission in chimeric pigs, the offspring failed to live (West et al., 2010, 2011). Why ES cells and iPS cells have been so challenging outside of rodent species is not clear, but possible ...
here. - Signet
here. - Signet

... Traditionally it has been believed that scurs are sex-influenced due to the fact that they have been shown to be more common in bulls than cows. An example of this is that when Aberdeen Angus cattle are crossed with Brown Swiss the result is scurred bulls and smooth polled (non-scurred) cows. Simil ...
Leukaemia Section t(3;9)(q27;p13) GRHPR/BCL6  Atlas of Genetics and Cytogenetics
Leukaemia Section t(3;9)(q27;p13) GRHPR/BCL6 Atlas of Genetics and Cytogenetics

... Prot) which mediates homodimerization and proteinprotein interactions with other corepressors (including HDAC1 and NCOR2/SMRT to constitute a large repressing complex, another transcription repression domain (191-386), PEST sequences (300-417) with a KKYK motif (375-379), and six zinc finger at the ...
Chapter 23: Population Genetics
Chapter 23: Population Genetics

... Genetic variation must exist for natural selection to occur much of the genetic variation in a population will produce no selective advantage – called neutral variation ...
Chapter 11 Mutation: The Source of Genetic Variation
Chapter 11 Mutation: The Source of Genetic Variation

... Genomic Imprinting • Expression of the gene depends on whether it is inherited from the mother or the father • Genes are marked during gamete formation or early embryonic development • The mechanism is not clearly understood • Does not affect all genes • Not a mutation, but a modification of the DN ...
Exploring Data using Dimension Reduction and Clustering
Exploring Data using Dimension Reduction and Clustering

... 2. Points can move from one cluster to another, but the final solution depends strongly on centroid initialization (so we usually restart several times to check). 3. If two centroids are equally (and maximally) close to an observation at a given iteration, we have to choose arbitrarily (the problem ...
17 - Rutgers Chemistry
17 - Rutgers Chemistry

... With reporter gene assays, different regulatory sequences (enhancers and/or promoters) can be tested to determine if they control expression of the target gene in different cells. For example, Figure 3 shows that regulatory sequence 3 activates the target gene in cell B; regulatory sequence 2 activa ...
Gene Section CDX2 (caudal-related homeobox 2) Atlas of Genetics and Cytogenetics
Gene Section CDX2 (caudal-related homeobox 2) Atlas of Genetics and Cytogenetics

... Found to be mutated in rare cases of colorectal carcinoma. ...
Ch 23 Evolution - philipdarrenjones.com
Ch 23 Evolution - philipdarrenjones.com

... number  of  alleles  at  a  locus     •  Is  the  total  number  of   individuals  x  2     •  The  total  number  of  dominant   alleles  at  a  locus     •  Is  2  alleles  for  each  homozygous   dominant  individual     •  Plu ...
Mr. Charles Montgomery Burns (Cellular Aging)
Mr. Charles Montgomery Burns (Cellular Aging)

... Sirtuins may protect against acetylation of molecules (ie. histone proteins) that may cause interference with normal function Nutrition: evidence to suggest that dietary caloric restriction can reduce incidence of certain age-related diseases and increase longevity in short-lived mammals (ie. rats) ...
Chapter 1 A Perspective on Human Genetics
Chapter 1 A Perspective on Human Genetics

... Genomic Imprinting • Expression of the gene depends on whether it is inherited from the mother or the father • Genes are marked during gamete formation or early embryonic development • The mechanism is not clearly understood • Does not affect all genes • Not a mutation, but a modification of the DN ...
A Long-Term Evolutionary Pressure on the Amount of Noncoding DNA
A Long-Term Evolutionary Pressure on the Amount of Noncoding DNA

... proportion of the offspring keep the ancestral phenotype by bearing no mutation or only neutral ones (Van Nimwegen et al. 1999; Wilke 2001a, 2001b; Wilke et al. 2001). Indeed, if the ancestral fitness cannot be retained from one generation to the next because deleterious mutations are too frequent, ...
Molecular studies on an ancient gene encoding
Molecular studies on an ancient gene encoding

Case Report Section
Case Report Section

... the karyotype 46,Y,t(X;11)(q22;q23) in 25 out of 30 metaphases. Fluorescence in situ hybridization study showed rearrangement of the MLL gene in interphase and metaphase cells revealing that the break-apart 5'MLL segment is translocated to the derivative X chromosome. The patient achieved a complete ...
Unit 2 Lesson 4 - Park Rapids school
Unit 2 Lesson 4 - Park Rapids school

The gene responsible for Clouston hidrotic
The gene responsible for Clouston hidrotic

... DFNB1 (29) and dominant DFNA3 (30), also map to the region containing the HED locus and show linkage to D13S175, D13S143 and D13S115. These two diseases result from an endocochlear defect and the responsible genes may code for one of the proteins involved in cochlea structure and function. Because c ...
Nematode genome evolution
Nematode genome evolution

... of sequence matches to Brugia malayi BAC end sequences (Whitton et al., 2004). 3.4. The effect of co-expressed genes on chromosomal evolution There are ~1000 operons in the C. elegans genome, of which 96% are conserved in C. briggsae, far more than expected if selection selection did not act to pres ...
Evolutionary Computation: Genetic Algorithms
Evolutionary Computation: Genetic Algorithms

... new population through genetic operations, and repeating this process a number of times. ■ We will start with Genetic Algorithms (GAs) as most of the other evolutionary algorithms can be viewed as variations of genetic algorithms. ...
Colorado Potato Breeding and Selection Program
Colorado Potato Breeding and Selection Program

... Fig. 1 PCR-based marker phenotypes used for MAS. The resistance locus and the linked marker are shown on the left of each panel. The diagnostic DNA fragment for each resistance locus is indicated by its approximate size in base pairs shown on the right. The first three lanes from the left in each p ...
Integrative Genome-wide Analysis of the Determinants of RNA
Integrative Genome-wide Analysis of the Determinants of RNA

... Since each event can represent the same transcript structure, these events are certainly not independent leading to exon skip events in 5, 623 genes, 3, 703 genes with alternative 3’-ends and 3, 278 genes showing alternative 5’ ends. After a very conservative correction (p-value <5 · 10−9 and 5% eff ...
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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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