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RT2 Profiler PCR Arrays: Pathway-focused gene
RT2 Profiler PCR Arrays: Pathway-focused gene

... pathway or disease state and three RNA quality control elements (see Figure 2 for the layout of a typical RT2 Profiler PCR Array). Researchers are able to focus on genes related to their biological pathway or disease state with our pre-designed pathway- or application-specific gene panels. By limiti ...
Gene Section MINA (MYC induced nuclear antigen) Atlas of Genetics and Cytogenetics
Gene Section MINA (MYC induced nuclear antigen) Atlas of Genetics and Cytogenetics

... The human MINA coding sequence consists of 1398 bp from the start codon to the stop codon. In addition to the 1395 bp-coding sequence, multiple alternative spliced transcript variants have been found for this gene. c-MYC protein stimulates the transcription of MINA through the E-box near the transcr ...
PTC_241Lecture005Cells
PTC_241Lecture005Cells

... have to bind transcription factors in order for transcription to take place. So protein synthesis just doesn’t happen willy nilly. It’s only activated when certain kind of factors bind to the chromosome and start transcription. So it’s a switch that turns transcription on, turns transcription off. S ...
complex patterns of inheritance
complex patterns of inheritance

... As we have just seen, an epistatic interaction causes the alleles of one gene to mask the effects of a different gene. Let’s now turn to another way that the alleles of different genes may affect the phenotype of a single trait. In many cases, the effects of alleles may be additive. This has been ob ...
CRISPR-Cas9 Mouse Toolbox
CRISPR-Cas9 Mouse Toolbox

... List of plasmids described below: 1. AAV:ITR-U6-sgRNA(Kras)-U6-sgRNA(p53)-U6-sgRNA(Lkb1)-pEFS-Rluc-2A-Cre-shortPAKrasG12D_HDRdonor-ITR (AAV-KPL) 2. AAV:ITR-U6-sgRNA(LacZ)-pEFS-Rluc-2A-Cre-WPRE-hGHpA-ITR 3. AAV:ITR-U6-sgRNA(backbone)-pEFS-Rluc-2A-Cre-WPRE-hGHpA-ITR 4. AAV:ITR-U6-sgRNA(NeuN)-pCBh-Cre- ...
Speciation genes in plants - Oxford Academic
Speciation genes in plants - Oxford Academic

... isolation (RI) between populations (Orr and Presgraves, 2000; Butlin and Ritchie, 2001; Noor, 2003; Orr et al., 2004; Rieseberg et al., 2004; Noor and Feder, 2006; Mallet, 2006; Bomblies and Weigel, 2007b; Rieseberg and Willis, 2007; Bomblies, 2010; Presgraves, 2010). These so-called ‘speciation gen ...


... mechanisms of macrophage parasitism by M. tuberculosis. We used signature tag transposon mutagenesis (STM) and a strategy of allelic replacement to identify M. tuberculosis genes involved in the ability of the bacillus to parasitise human macrophages. The inactivation of the two two-component signal ...
Investigation 9: Genetic Variation
Investigation 9: Genetic Variation

... • We’ve seen the traits in a population of walkingsticks change over the course of several generations. Today we are going to start an investigation into the question of just how that kind of change can happen in a population. ...
Word - The Open University
Word - The Open University

... 1 Genetic medicine: dreams and realities Genetics can be used in medicine to confirm a previous or make a fresh diagnosis, or predict a disorder likely to occur in future. At the moment, that is often all that can be done. The so-called ‘diagnostic therapeutic gap’ is one immediate problem for us to ...
One of the crucial proteins to influence type 2 diabetes
One of the crucial proteins to influence type 2 diabetes

... hand, HMGA1 and INSR expressions decrease in diabetic carriers of IVS5-13insC compared with those of wild-type diabetic and non-diabetic patients(Chiefari, et al., 2011). INSR protein expression and insulin-binding capacity are also restored in lymphoblasts obtained from diabetic IVS5-13insC carrier ...
Applied Environmnetal Microbiology
Applied Environmnetal Microbiology

... fivefold in 10 mM Tris-HCl (pH 8.0) buffer containing 1 mM phenylmethylsulfonyl fluoride, and the cells were disrupted by ultrasonic treatment until lysis was complete. The lysates were then centrifuged at 10,000 3 g to collect the inclusion bodies, and, finally, the pellet was suspended at 1/10 the ...
Expanding Yeast Knowledge Online.
Expanding Yeast Knowledge Online.

... genome, the genes it contains and their interactions. SGD provides current, annotated yeast sequence through the WWW and via FTP. In addition to providing an on-line genome database, SGD also provides access to other information of interest to the budding yeast community. SGD is responsible for main ...
Article The Pseudoautosomal Regions of the U/V Sex
Article The Pseudoautosomal Regions of the U/V Sex

... size (Spearman’s correlation test  = 0.113, P = 0.598) whereas gene density and GC percentage increase with ...
Précis - Scoliosis and Spinal Disorders
Précis - Scoliosis and Spinal Disorders

... for three loci on chromosome 6p, distal 10q, and 18q [23]. Another study found a linkage with IS at locus 17p11 in a three generation IS Italian family 9 and another linkage with IS was found at locus 19p13.3 in a Chinese family [11]. A recent study reports that also an X-linked susceptibility locus ...
assoc_intro
assoc_intro

... This can only lead to underpowered studies and inflated expectations •We should concern ourselves with the apparent effect size at the marker, which results from 1) difference in frequency of marker and trait alleles 2) LD between the marker and trait loci 3) effect size of trait allele ...
Problem Set 2 The purpose of this problem set is to familiarize
Problem Set 2 The purpose of this problem set is to familiarize

... Gene ID for that gene. To do this, you should create a simple python script that uses a dictionary to translate RefSeq IDs in a bed file to Entrez IDs provided in a translation file. We have created a file with RefSeq IDs and their associated Entrez Gene ID in DATA/PS2/Prom_with_Entrez.txt. Note ...
Bowel Cancer and Inherited Predisposition
Bowel Cancer and Inherited Predisposition

... Variations to the information in one of these ‘cancer protection’ genes such as a breast or bowel cell may cause the process of cell division to be less well controlled and cells may grow and divide abnormally. A variation that makes the gene faulty is called a mutation or a pathogenic variant. Muta ...
Morphogenesis of Flowers—Our Evolving View
Morphogenesis of Flowers—Our Evolving View

... and ensured that seeds subsequently developed. He concluded that petals were not involved because many flowers lack petals but set seeds (e.g., vines and cereals), and also some garden plant variants had extra petals at the expense of stamens (double flowers), and even though these may have styles, ...
Detection of Five Rare Cystic Fibrosis Mutations Peculiar to
Detection of Five Rare Cystic Fibrosis Mutations Peculiar to

... the one most distant from the CFTR gene. A recombinant event between the XV2c locus and the CFTR gene is not inconceivable. The mutation detected in the second French patient could derive from a second, more recent, recombinant event within the CFTR gene, between exons 8 and 19. The mutation detecti ...
ISMB2008PosterManagingGenomicData
ISMB2008PosterManagingGenomicData

... GMOD supports visualizing comparative genomics data. Sybil shows syntenic regions and whole genome comparisons. CMap shows comparative maps of any type (genetic, physical, sequence, …). SynView (shown), GBrowse_syn and SynBrowse are GBrowsebased synteny browsers. ...
Identification of Potential Corynebacterium ammoniagenes Purine
Identification of Potential Corynebacterium ammoniagenes Purine

... C. ammoniagenes gDNA Clones in E. coli The dependence of purines in the regulation of purE-lacZ and purF-lacZ was characterized by the candidate C. ammoniagenes gDNA clones involved in pur reporter repression. The 3 candidate clones (“E-7”, “E-32”, and “E-33”) strongly repressed purE-lacZ expression ...
unit II - SP College
unit II - SP College

... Satellite DNA adopts higher-order three-dimensional structures in eukaryotic organisms. This was demonstrated in the land crab Gecarcinuslateralis, whose DNA contains 3% of a GC-rich sequence consisting of repeats of a ~2100 base pair (bp) sequence called RU. The RU was arranged in long tandem array ...
Mutations at the Darkener of apricot Locus Modulate Transcript
Mutations at the Darkener of apricot Locus Modulate Transcript

... of wing-structure was compared among the four classes of wing tissue, Doa mutant heterozygotes intermediate segregants in the F1 generation. Since the Bx locus is X amounts, and Doa heteroallelic flies the most. Other linked, F, males were hemizygous for Bx'~,and females were Bx alleles similarly te ...
Familial Adenomatous Polyposis (FAP)
Familial Adenomatous Polyposis (FAP)

... If we think of a gene as a long word carrying a message, then the FAP gene has nearly 9000 letters in it. In different families it is a different letter or group of letters which have been wrongly copied which causes the gene not to work. The genetics team will try to work this out for each family, ...
Supplementary Infomation (doc 1650K)
Supplementary Infomation (doc 1650K)

... downstream of rs12649507, earlier associated with SDav1) for associations with SDav in the discovery meta-analysis (−log10 P values on the y axis and the SNP genomic position on the x axis). We could confirm the earlier association of rs12649507 or rs11932595 with SDav (only had imputed genotypes) i ...
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RNA-Seq



RNA-seq (RNA sequencing), also called whole transcriptome shotgun sequencing (WTSS), is a technology that uses the capabilities of next-generation sequencing to reveal a snapshot of RNA presence and quantity from a genome at a given moment in time.
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