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bio12_sm_07_5
bio12_sm_07_5

... 9. (a) The CAG trinucleotide is the repeated sequence linked to Huntington’s disease. (b) The probable onset of Huntington’s occurs between 30 and 70 repeats. (c) The more repeats there are, the greater the effect of the gene. Normal individuals have 9 to 34 repeats. More repeats than this causes th ...
13-3 Cell Transformation
13-3 Cell Transformation

Bioinformatics and its applications
Bioinformatics and its applications

APS Science Curriculum Unit Planner
APS Science Curriculum Unit Planner

... combinations in offspring. Genetic recombination and mutations may or may not alter phenotypes. Altered phenotypes may or may not be deleterious.  7.1 Some traits are sex-linked.  7.2 Phenotype is affected by many different factors. Students will understand how some alleles interact with each othe ...
Cancer-Causing-Foods-1
Cancer-Causing-Foods-1

... suppress that gene that carcinogen will eventually affect 0:00:31.0 cancer sa family. I am just kidding. That is partly because of the gene. Kung manganak 0:00:48.5 only the women who give more time and effort in the early years 0:01:00.8 mga 35 dahil unahun kan career. This lifestyle is a choice an ...
COMPLEX PATTERNS OF INHERITANCE
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Lecture#3 Genes encode Proteins Readings: Problems: Concepts
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... Note: the entire model was inferred from the properties of the mutants (phenotype) - later the presence of defective enzymes was demonstrated by independent biochemical analysis History - first insight into the function of genes and how they worked (remember it wasn't until 1944 that DNA was shown t ...
bioinformatics_project
bioinformatics_project

... (ssODN) as a template. sgRNA sequences typically have the form G(N19)NGG. Cas9 nicks before NGG, which is also known as the protospacer adjacent motif, or PAM sequence. Ideally, the mutation is as close as possible to the sgRNA site without being within it so that it does not interfere with sgRNA bi ...
Gene Section TP53 (tumor protein p53 (Li-Fraumeni syndrome)) in Oncology and Haematology
Gene Section TP53 (tumor protein p53 (Li-Fraumeni syndrome)) in Oncology and Haematology

... Autosomal dominant condition, cancer prone disease, Li-Fraumeni syndrome (LFS) is defined by the existence of a proband with early onset sarcoma and a first degree relative with cancer before 45 years, plus another first/second degree relative with cancer at before 45 years or sarcoma at any age. Cl ...
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Gene Section RB1 (retinoblastoma) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... nuclear proteins with significant sequence similarity in two discontinuous areas (pockets domains); conditional on the phosphorylation status, these pocket proteins can bind transforming proteins of DNA tumor viruses as well as nuclear proteins. ...
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Brittany Barreto, Drew `13, Baylor College of Medicine”Role of small

... Organisms evolve under stressful conditions by increasing mutation rate through stress-induced mutagenesis (SIM). A prominent mechanism of SIM in Escherichia coli is mutagenic DNA break repair, in which repair of DNA double-strand breaks by homologous recombination becomes error-prone. Mutagenic bre ...
Breast Cancer - Wk 1-2
Breast Cancer - Wk 1-2

... CHEMOTHERAPY  As well as radiation most cancer treatment is followed with either or chemotherapy and hormonal therapy  Chemotherapy consists of administration of medicine, usually either orally or IV, for treatment of cancer  Chemotherapy and hormonal therapy are the only therapies that treat the ...
Slide 1
Slide 1

... combining withfrom yourtheir partner’s one from their dad. We will look at size genes today. Turn over the cards to see which gene characteristics (allelles) your lambfrom will carry Each remove the two size gene cards the pack and place them Record your lamb’s gene characteristics on your sheet col ...
Chapter 15 Power Point Slides
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Biology 303 EXAM II 3/14/00 NAME
Biology 303 EXAM II 3/14/00 NAME

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Deoxyribonucleic Acid (DNA)
Deoxyribonucleic Acid (DNA)

... Deoxyribonucleic Acid (DNA) Deoxyribonucleic acid (DNA) is the chemical compound that contains the instructions needed to develop and direct the activities of nearly all living organisms. DNA molecules are made of two twisting, paired strands, often referred to as a double helix. Each DNA strand is ...
Molecular genetics of gene expression
Molecular genetics of gene expression

... Consider the possibility that you are employed by an agricultural biotechnology company, and they ask you to find a bacterial gene for resistance to a specific herbicide. The herbicide has been manufactured by the company for many years. Using a strategy similar to that used to find glyphosate resis ...
Biotechnology and Genetic Engineering
Biotechnology and Genetic Engineering

... tumefaciens causes crown gall disease by first transferring part of its DNA into an opening in the plant. The DNA then integrates itself into the plant's genome and causes the formation of the gall. ...
Gene Section chromosomal) isoform I and Y) Atlas of Genetics and Cytogenetics
Gene Section chromosomal) isoform I and Y) Atlas of Genetics and Cytogenetics

... receptor a-chain, the chemokine MGSA/GRO, and the class II major histocompatibility complex gene HLADRA; negative regulation by binding the promoter regions of interleukin-4 and GP91-PHOX. The precise function remains to be elucidated; probable role in regulation of chromatin structure and gene expr ...
ASSIGNMENT – 1
ASSIGNMENT – 1

... 25. A certain kind of cattle have two genes of coat colour, R for red, and r for white. When an individual cow is heterozygous, it is spotted with red (roan). When two red genes are present, it is red. When two white genes are present, it is white. The gene H for lack of horns is dominant over h for ...
EOC Practice Quiz (5) - Duplin County Schools
EOC Practice Quiz (5) - Duplin County Schools

Deoxyribonucleic Acid (DNA)
Deoxyribonucleic Acid (DNA)

... Deoxyribonucleic Acid (DNA) Deoxyribonucleic acid (DNA) is the chemical compound that contains the instructions needed to develop and direct the activities of nearly all living organisms. DNA molecules are made of two twisting, paired strands, often referred to as a double helix. Each DNA strand is ...
 
 

... Deletion  of  this  gene  from  F. pseudograminearum  resulted  in  a  reduction  in  virulence  on  barley  and  virulence  could  be  restored  by  expression  of  the  wild  type  coding  sequence,  indicating  this  is  a  novel  virulence  gene.  Population surveys suggest the gene has been pre ...
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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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