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chapter10
chapter10

... • Most of the 1,336 genes on the X chromosome determine nonsexual traits such as blood clotting and color perception • The human Y chromosome carries 307 genes, including SRY – the master gene that triggers formation of testes in males • Testosterone produced by the testes causes formation of male g ...
BioSc 231 Exam 2 2003
BioSc 231 Exam 2 2003

... (5) In corn, the genes v, b and l are linked. The data given below summarize the result of a three-point testcross. From the data, construct a map showing the genes in the correct order and indicating the distances between each pair of genes. ...
Number 4 - Laboratory Animal Boards Study Group
Number 4 - Laboratory Animal Boards Study Group

... information about the problem, 3) formulate a hypothesis that can be tested, 4) gather objective data to test the hypothesis, and 5) interpret the data in regard to the identified problem. However, funding agencies require hypotheses in the proposal, perhaps assuming steps 1 & 2 were already carried ...
The Respiratory System
The Respiratory System

... You can live with only one lung, and often that lung will develop and get stronger When you smoke ANYTHING, you are coating the lining of your lungs with tar and other substances that block/prevent oxygen from getting to the blood/body Pneumonia - build up of fluid in the lungs, thereby prevent oxyg ...
Breast Cancer - Deanna Bennett
Breast Cancer - Deanna Bennett

sheet#12,Dr Faleh,Raghad Alawnah
sheet#12,Dr Faleh,Raghad Alawnah

... -Second cause of oral cancer -Relative risk: dose; duration, quality -When the dose (high) , long duration , poor quality >> more carcinogenic by-product >> oral cancer -In the west: the percentage of oral cancer high because of smoking and alcohol at the same time. -Mechanism of alcohol to cause or ...
Assessment of space-radiation effects on immune function on the
Assessment of space-radiation effects on immune function on the

... Epidermal growth factor receptor (EGFR) is well known for its crucial roles in cell differentiation/proliferation and development/progression of cancer (especially lung and breast cancers), and recent studies have suggested that EGFR may be engaged in the regulation of chemokine genes’ expression an ...
FocalScan: Scanning for altered genes in cancer based on
FocalScan: Scanning for altered genes in cancer based on

... gions recur at roughly the same position in multiple independent tumor samples (‘focal regions’). Such patterns indicate selection for altered expression of genes that may drive oncogenesis (oncogenes) or hinder cancer growth (tumor suppressors). Tools have therefore been developed to find these fre ...
Slide ()
Slide ()

... Model to generate a wild-type BLM locus via somatic intragenic recombination: I, The two pairs of sister chromatids of the homologous chromosome Nos. 15 in a G2 somatic cell of a BS genetic compound (blm1 /blm2 ) are numbered 1-1 to 4-4. Each of the two mutations in BLM (the hatched rectangle), repr ...
microarray data analysis using r programming
microarray data analysis using r programming

... represents a part of a cell lumen, extracellular region, membrane, macromolecular complex as shown in fig.20. Similar result analysis for 3 group data set is carried out. ...
Hox
Hox

... Each cell has to have 1. information: where it is relative to other cells 2. where it is in the developmental sequence. Information provided by Homeotic genes (Hox genes) ...
Mcbio 316: Exam 1A Answers (10)1. A wild
Mcbio 316: Exam 1A Answers (10)1. A wild

Fig1 from Nature Rev Mol. Cell Biol (Nov2003) 4(11):865
Fig1 from Nature Rev Mol. Cell Biol (Nov2003) 4(11):865

Honors Genetics Chapter 4 Vocabulary We learned several new
Honors Genetics Chapter 4 Vocabulary We learned several new

Mrs PC, 63yo woman - Oncology Clinics Victoria
Mrs PC, 63yo woman - Oncology Clinics Victoria

...  Results of initial stains inform selection of further stains  The amount of tissue is often a limiting factor  IHC staining algorithms have been shown to predict the primary site correctly in approximately two thirds of ...
SARSIA
SARSIA

... We have developed a protocol to perform a genetic screen for zygotic mutations affecting embryogenesis on the protochordate Ciona intestinalis. The choice of this taxon, whose phylogenetic position places it at the basis of the chordates as one the most primitive vertebrate relatives, could allow to ...
Human genomes - The University of Auckland
Human genomes - The University of Auckland

... analysis and storage requirements have posed significant challenges to traditionally data-poor biomedical analysis. ...
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... Combining genetic analysis with FACS ...
KEY UNIT TWO TEST – STUDY GUIDE Define primer. A short piece
KEY UNIT TWO TEST – STUDY GUIDE Define primer. A short piece

Chapter 13 DNA Technology
Chapter 13 DNA Technology

... 1. Transfer, along with the foreign gene, the promoter sequences that turn the gene on. 2. Insert the foreign gene beside a gene that is normally expressed in large quantities within the host cell. Hopefully the foreign gene will be expressed along with the frequently expressed gene. ...
Click to add title - University of Iowa
Click to add title - University of Iowa

... • Although it is usually due to cis-acting regulatory regions, some are due to trans-action ...
Epidermal Growth Factor Receptor and K
Epidermal Growth Factor Receptor and K

...  Only 2 patients found to have EGFR mutations  3 patients without EGFR mutations responded to treatment  But 4/23 patients prevented from unnecessary treatment  Given that erlotinib is effective in only 10-20% of NSCLC patients selection ...
Overexpression of DNA repair genes is associated with metastasis
Overexpression of DNA repair genes is associated with metastasis

... [22,23]. If this result can be translated to human tumours, this would indicate that highly mutagenized primary tumour cells have difficulties to move and colonize distant organs in other environment. Stabilization of the mutator phenotype in a large sense or increased DNA repair could be a way to a ...
Genetics 314 – Spring 2006
Genetics 314 – Spring 2006

Causes, Risks, Prevention
Causes, Risks, Prevention

... rather than having been inherited. These acquired gene mutations sometimes result from exposure to cancer-causing chemicals (like those found in tobacco smoke). But often what causes these changes is not known. Many gene changes are probably just random events that sometimes happen inside a cell, wi ...
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Oncogenomics



Oncogenomics is a relatively new sub-field of genomics that applies high throughput technologies to characterize genes associated with cancer. Oncogenomics is synonymous with ""cancer genomics"". Cancer is a genetic disease caused by accumulation of mutations to DNA leading to unrestrained cell proliferation and neoplasm formation. The goal of oncogenomics is to identify new oncogenes or tumor suppressor genes that may provide new insights into cancer diagnosis, predicting clinical outcome of cancers, and new targets for cancer therapies. The success of targeted cancer therapies such as Gleevec, Herceptin, and Avastin raised the hope for oncogenomics to elucidate new targets for cancer treatment.Besides understanding the underlying genetic mechanisms that initiates or drives cancer progression, one of the main goals of oncogenomics is to allow for the development of personalized cancer treatment. Cancer develops due to an accumulation of mutations in DNA. These mutations accumulate randomly, and thus, different DNA mutations and mutation combinations exist between different individuals with the same type of cancer. Thus, identifying and targeting specific mutations which have occurred in an individual patient may lead to increased efficacy of cancer therapy.The completion of the Human Genome Project has greatly facilitated the field of oncogenomics and has increased the abilities of researchers to find cancer causing genes. In addition, the sequencing technologies now available for sequence generation and data analysis have been applied to the study of oncogenomics. With the amount of research conducted on cancer genomes and the accumulation of databases documenting the mutational changes, it has been predicted that the most important cancer-causing mutations, rearrangements, and altered expression levels will be cataloged and well characterized within the next decade.Cancer research may look either on the genomic level at DNA mutations, the epigenetic level at methylation or histone modification changes, the transcription level at altered levels of gene expression, or the protein level at altered levels of protein abundance and function in cancer cells. Oncogenomics focuses on the genomic, epigenomic, and transcript level alterations in cancer.
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