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Novel genetic aspects of Klinefelter`s syndrome
Novel genetic aspects of Klinefelter`s syndrome

... The human X chromosome, inactivation and gene-dosage The human sex chromosomes (X and Y) originate from an ancestral homologous chromosome pair, which during mammalian evolution lost homology due to progressive degradation of the Y chromosome (Charlesworth and Charlesworth, 2005; Graves, 2006). In a ...
Efficient Ends-Out Gene Targeting In Drosophila
Efficient Ends-Out Gene Targeting In Drosophila

... marker with a GFP marker, or replacing wild type loxP sites with other lox site variants. pRK2 was generated by adding GMR enhancer into the BsiWI site of pRK1. In addition, enzyme sites in 5' MCS are ordered similarly to the popular pUAST vector. Thus, when pRK1 or pRK2 is used for making knock-in ...
population
population

... • Sexual reproduction can shuffle existing alleles into new combinations • In organisms that reproduce sexually, recombination of alleles is more important than mutation in producing the genetic differences that make adaptation possible 有性生殖導致基因重組 增加適應性 ...
Dosyayı İndir
Dosyayı İndir

... The order of genes along the chromosome can be deduced by determining the genes transferred during short matings vs. those transferred during long matings Copyright ©The McGraw-Hill Companies, Inc. Permission required for reproduction or display ...
Designing Microarray Experiments
Designing Microarray Experiments

... which may be specific to tissues or conditions. So many of the genes may differentially express It is important to keep the coverage of the array broad in the sense that genes come from many different expression studies. It is important to include “house-keeping” genes on the array. Genes which are ...
Genetics introduction
Genetics introduction

... •Genotype of each parent? •What is the genotypic ratio? •What is the phenotypic ratio? •What percentage of the F1 generation will have a heterozygous genotype? •What is the probability that the 5th puppy will have a pink nose? ...
BROWSING GENES AND GENOMES WITH ENSEMBL
BROWSING GENES AND GENOMES WITH ENSEMBL

... 8 Type ‘refseq’ in the ‘Find a track’ text box. 8 Select ‘RefSeq import – Expanded with labels’. 8 Click (P). 8 Click on individual transcript models to retrieve more information about them. There has been one transcript annotated by RefSeq for the BRCA2 gene, i.e. NM_000059.3. This transcript ...
Naming `junk`: Human non-protein coding RNA (ncRNA) gene
Naming `junk`: Human non-protein coding RNA (ncRNA) gene

... Previously, the majority of the human genome was thought to be ‘junk’ DNA with no functional purpose. Over the past decade, the field of RNA research has rapidly expanded, with a concomitant increase in the number of non-protein coding RNA (ncRNA) genes identified in this ‘junk’. Many of the encoded ...
Two distinct teleost hepatocyte nuclear factor 1 genes, hnf1a/tcf1
Two distinct teleost hepatocyte nuclear factor 1 genes, hnf1a/tcf1

... by using TRIZOL reagent (Invitrogen). Using 1 Ag of total RNA, the first-strand cDNAs (20 Al) were synthesized with oligo(dT) by SUPERSCRIPT III reverse transcriptase (Invitrogen) according to manufacturer’s protocol. After reverse transcription, 2-Al first-strand cDNAs were subjected to PCR by usin ...
Expansion of the Pseudo-autosomal Region and Ongoing
Expansion of the Pseudo-autosomal Region and Ongoing

... SA polymorphism hypothesis for recombination suppression, a genetic map is essential, together with comparative maps from related species without sex chromosomes. Ideally such mapping work should be based on markers in functional genes to identify orthologous genes for comparative mapping, which can ...
Supplementary Data File Supplementary Figures Figure S1
Supplementary Data File Supplementary Figures Figure S1

... Figure S1. Hypothetical example of variability count distributions for a pathway and a reference. A. The reference distribution corresponds to a hypothetical data set with 10,000 genes where 2,500 genes are in the low variability category, 5000 in the medium and 2500 in the high variability category ...


... (A) DNA gel blot of P. hybrida plants harboring the mutable an2-W82 allele (W82) or four independently derived An21 revertant alleles (R1 to R4) hybridized with the dTph1 flanking sequence jaf41. The size of the hybridizing fragments (in kilobases) is indicated at right. (B) Diagram showing the stru ...
Plasmodium malariae and P. ovale genomes provide insights into
Plasmodium malariae and P. ovale genomes provide insights into

... hosts. As noted in previous comparative genomics studies involving host switches in the Plasmodium genus, invasion-related genes are consistently found to be rapidly evolving. The RBP family is highly expanded (Extended Data Fig. 4a) but its differential distribution across species suggests that RBP ...
of C. hortensis and C. nemoralis
of C. hortensis and C. nemoralis

... chromosomes shows a secondary constriction about half-way along one of its arms. A great many satellites and secondary constrictions are apparent in the chromosomes of C. hortensis (Fig. 2A, B) but as these are not a consistent feature of the karyotype and their demonstration is much dependent on tr ...
Identification of eight novel coagulation factor XIII subunit A
Identification of eight novel coagulation factor XIII subunit A

... mutations within F13B gene. In this study we present only the mutations in the F13A gene while the mutations for the F13B gene will be published separately. In addition, genetic analysis of FXIII genes was done in a single patient with severe FXIII deficiency (<5% of normal FXIII activity). The clin ...
The Heritability of happiness
The Heritability of happiness

... ‘Happiness depends, as Nature shows, less on exterior things than most suppose. ‘ - William Cowper ...
CDKN2 (p16/MTS1) Gene Deletion or CDK4
CDKN2 (p16/MTS1) Gene Deletion or CDK4

... tions had been identified previously among the anaplastic astrocyto mas, yet one case which had previously shown loss of one allele at the IFNa/w locus and 2 cases in which no losses had been identified at either locus were found to have homozygous deletions located be tween but not involving the D9 ...
Genetics
Genetics

... Percentages quoted in the slides are for a group of 100 trainee primary teachers on entry to ITE, having obtained a ‘C’ or better at GCSE, usually two or three years previously. This gives secondary trainees an insight into the misconceptions that survive a GCSE course, and all trainees some comfort ...
Molecular Mechanisms of Developmental Review
Molecular Mechanisms of Developmental Review

... major developmental landmarks that define the C. elegans life cycle. An answer to this question can be achieved by returning to an analogy described by Ambros and Horvitz (1987) and later extended by Slack and Ruvkun (1997). These authors proposed that temporal patterning is analogous to spatial pat ...
Mapping quantitative trait loci and expressed sequence tags related
Mapping quantitative trait loci and expressed sequence tags related

... 2001, Yang et al. 2002). However, the BPH resistance conferred by these major genes is not durable; for example, Bph1 and bph2 can be overcome by BPH biotypes 2 and 3 (Pathak and Heinrichs 1982, Panda and Khush 1995). In contrast, quantitative trait loci (QTLs) were found to confer more durable BPH ...
The Genetics of SMA - Families of SMA Canada
The Genetics of SMA - Families of SMA Canada

... contains the two SMN genes. The major difference between the two SMN gene copies is the C (SMN1) to T (SMN2) nucleotide change in exon 7 in their DNA. Because of this difference, SMN2 mostly makes mRNA message that excludes exon 7 and produces a smaller, unstable SMN protein. SMN1 makes mRNA message ...
Fluorescence in Situ Hybridization Evaluation of c-erbB
Fluorescence in Situ Hybridization Evaluation of c-erbB

... human cancers (1). A few studies using FISH showed c-erbB-2 gene amplification in bladder cancers, and the clinical significance of c-erbB-2 gene amplification is controversial. Sauter et al. (4) reported that c-erbB-2 gene amplification (defined as more than twice as many c-erbB-2 signals as centro ...
Genetics - Muscular Dystrophy Canada
Genetics - Muscular Dystrophy Canada

... contains the two SMN genes. The major difference between the two SMN gene copies is the C (SMN1) to T (SMN2) nucleotide change in exon 7 in their DNA. Because of this difference, SMN2 mostly makes mRNA message that excludes exon 7 and produces a smaller, unstable SMN protein. SMN1 makes mRNA message ...
Y chromosome polymorphisms in medicine
Y chromosome polymorphisms in medicine

... Among these, partial gene copy deletions of multicopy genes or rearrangements/inversions occurring in non-coding sequences but with possible functional effects on gene expression, are the most obvious candidates. These types of alterations may segregate with certain Y backgrounds, therefore the de®n ...
Document
Document

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Gene expression programming

In computer programming, gene expression programming (GEP) is an evolutionary algorithm that creates computer programs or models. These computer programs are complex tree structures that learn and adapt by changing their sizes, shapes, and composition, much like a living organism. And like living organisms, the computer programs of GEP are also encoded in simple linear chromosomes of fixed length. Thus, GEP is a genotype-phenotype system, benefiting from a simple genome to keep and transmit the genetic information and a complex phenotype to explore the environment and adapt to it.
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