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File - Amazing World of Science with Mr. Green
File - Amazing World of Science with Mr. Green

... comparison of BR-R and SU-R in graph 1. SU-R = 60% survival, BR-R = 45% / SU-R has higher survival than BR-R; SU-R offers more resistance than BR-R; Award [1 max] for any of the following which refer to the comparison of BR-R and SU-R in graph 2. BR-R performs (slightly) better when combined with SU ...
H63D: The Other Mutation - Iron Disorders Institute
H63D: The Other Mutation - Iron Disorders Institute

... especially when in combination with other mutations. C282Y/ S65C compound heterozygotes have demonstrated elevated serum iron indices and iron overload. When examined, H63D stands out as a significant modifier of disease onset, progression and even response to therapy. H63D is associated with arteri ...
H2 HomeFun Worksheet -Teacher`s Copy - CIA-Biology
H2 HomeFun Worksheet -Teacher`s Copy - CIA-Biology

... Date: _____________________ ...
Evolution: Hox genes and the cellared wine principle
Evolution: Hox genes and the cellared wine principle

... beetle gene fails to cause a segmentation defect, the role of this expression has not been clear [11]. It is reasonable to suppose that it performs a somewhat redundant function to that of the homeobox gene even skipped, which is expressed in every beetle segment but only the even-numbered fly segme ...
Chapter 11 Protein Characterization
Chapter 11 Protein Characterization

... Transgenic plants are plants possessing a single or multiple genes transferred from a different species. It refers to plants created in lab using recombinant DNA technology. Tumor inducing plasmids can be used to introduce new genes into plant cells. The TDNA segment of Ti plasmids can be integrate ...
Non-Mendelian Inheritance PPT
Non-Mendelian Inheritance PPT

... • Most of your traits are controlled by the interaction of many genes. • Multiple genes working together produce a continuous distribution in a “Bell Shape” curve of degrees. ...
Gene Section FOXQ1 (forkhead box Q1) Atlas of Genetics and Cytogenetics
Gene Section FOXQ1 (forkhead box Q1) Atlas of Genetics and Cytogenetics

... CA-AT at position 766-767. Foxq1sa-el has a point mutation a position 383 changing T to G thus replacing isoleucine with serin at position 128 in the protein. Foxq1sa-J has C to T mutation in position 490 changing the amino acide arginine to cysteine at position 164 in the protein (Hong et al., 2001 ...
Figure 1 - York College of Pennsylvania
Figure 1 - York College of Pennsylvania

... • Genes involved in neurodegeneration may also play a role in neurodevelopment (Bothwell and Giniger 2000). • The advantages to characterizing genes in zebrafish are their rapid development, translucent embryos, large clutches, and the development of in situ hybridization and morpholino knockdown te ...
Data
Data

... characterize the interactions among the input signals, and offer quantitative predictions for the observable variables. • Require more input data in general because of the large number of parameters to fit, as well as some type of understanding of the nature of the aggregation function. Most dynamic ...
Slides Part 2 PPTX
Slides Part 2 PPTX

... cancer signaling pathway can also serve as an organizing framework for interpreting microarray expression data. ...
sample - Mouse Genome Informatics
sample - Mouse Genome Informatics

...  Individual genes can also be studied using spontaneous mutations or targeted alleles  MGI currently lists over 39,000 mutant alleles that have been described in mice ...
Promoters - Pennsylvania State University
Promoters - Pennsylvania State University

... To what specific sequence in DNA does the protein bind ? (DNA Footprinting Assay) • A protein bound to a specific sequence within a DNA fragment will protect that sequence from cleavage by DNase or chemical reagents. • DNA outside the region of protein binding will be sensitive to cleavage. • After ...
Leukemia Section t(17;19)(q22;p13) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukemia Section t(17;19)(q22;p13) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... transcription factors E12 and E47; expressed in most cell types. ...
Gene Section MYST3 (MYST histone acetyltransferase (monocytic leukemia) 3
Gene Section MYST3 (MYST histone acetyltransferase (monocytic leukemia) 3

... 2004 amino acids; 225 kDa; composed from N-term of: a NEMM domain (N-term region of ENOK, MOZ or MORF) including a H15 (linker H1 and H5 like) nuclear localization domain, 2 PHD (plant homeodomain, also known as LAP (leukemia ...
Welcome to the Gene and Allele Database Tutorial
Welcome to the Gene and Allele Database Tutorial

... Associated Data is under the Gene detail. The number represent numbers of associations. Click a category to expand the table and access that data in Gramene (see slides 8–13). Grayed-out categories have no associations. ...
What are transcription factors?
What are transcription factors?

... luckily there are 2 tall people living at your house.  It is also a difficult light switch to turn on, so 2 people need to work together to turn it on.  In order to make light/gene product, you need the STAT to exist as a dimer (two STATs bound together). In our analogy, that means we need two peo ...
Part B - Bioinformatics
Part B - Bioinformatics

... Error rates ignore temporal information such as when a patient dies. Survival analysis takes temporal information into account. The Kaplan-Meier survival plots and statistics for the above predictions show significance. ...
Inserting a Competency Regulatory Gene into E. coli
Inserting a Competency Regulatory Gene into E. coli

... My Focus Insulin Gene Extracted ...
Gaining biological specificity in gene set analysis by correcting for
Gaining biological specificity in gene set analysis by correcting for

...  Most results are based on ranking GO terms  Only small percentage is expected to be significant and relevant  Need to add similar comparisons considering only significant GO terms or comparing the actual p-values ...
Common Dominant and Recessive Traits in Humans
Common Dominant and Recessive Traits in Humans

... that is seen due to presence of a recessive allele located on the X chromosome. There are two X chromosome in women and one of them usually carries an allele for normal vision. In men, there is only one X chromosome and if they carry an allele for color blindness, they will express this trait. This ...
Slide 1
Slide 1

... A synthetic, 23-bp ecdysterone regulatory element (EcRE) , derived from the upstream region of the Drosophila melanogaster hsp27 gene, was inserted adjacent to the herpes simplex virus thymidine kinase promoter fused to a bacterial gene for chloramphenicol acetyltransferase (CAT). ...
Identifying essential genes in M. tuberculosis by random
Identifying essential genes in M. tuberculosis by random

... Goal: Estimate Pr( | m). • Begin with some initial assignment, (0), ensuring that i(0) = 1 whenever mi > 0. • For iteration s, consider each gene one at a time and ...
Here
Here

... module has a certain function (Fig. 4). A list of modules and their regulators was then processed using the program Cytoscape, which created a module-regulator network map, with modules in light blue and regulators in orange (Fig. 5). ...
ppt
ppt

... Tel-Aviv University ...
Development of insect-resistant transgenic cabbage plants
Development of insect-resistant transgenic cabbage plants

... mortality and leaf area damage observed among the different transgenic lines could be correlated to differences in Bt gene expression. The larvae fed on transgenic leaf discs were severely stunted in growth when compared to larvae fed on wild type leaf (Figure 6). At whole plant level also, transgen ...
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Epigenetics of diabetes Type 2

In recent years it has become apparent that the environment and underlying mechanisms affect gene expression and the genome outside of the central dogma of biology. It has been found that many Epigenetic mechanisms are involved in the regulation and expression of genes such as DNA methylation and chromatin remodeling. These epigenetic mechanisms are believed to be a contributing factor to pathological diseases such as Diabetes type II. An understanding of the epigenome of Diabetes patients may help to elucidate otherwise hidden causes of this disease.
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