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Cool Stuff About DNA
Cool Stuff About DNA

... More than 200 genes in the human genome have a bacterial ancestry. ...
Repair of DNA double-strand breaks and susceptibility to breast
Repair of DNA double-strand breaks and susceptibility to breast

Unit2Day5
Unit2Day5

... 169 different genes with expression differences between human and chimp in cortex Most genes were more highly expressed in human vs. chimp Caceres et al., 2003, PNAS, 100: 13030-13035 ...
Ch. 13 Meiosis
Ch. 13 Meiosis

... • Almost all of the DNA in a eukaryotic cells is subdivided into chromosomes in the nucleus. • Tiny amounts of DNA are found in mitochondria and chloroplasts. ...
BootcampNotes2014
BootcampNotes2014

... • Show genes as superscript. • Most sex-linked disorders are recessive. ...
Chapter 24
Chapter 24

... 25. Explain how gene expression profiling differs from studying mutations in a single gene. (p. 933) Gene expression profiling considers suites of genes whose functioning underlies cell survival and specialization as well as how cells interact as they respond to the environment and form tissues. 26. ...
HGP102new
HGP102new

... • Noncoding DNA types, amount, distribution, information content, and functions • Coordination of gene expression, protein synthesis, and post-translational events • Interaction of proteins in complex molecular machines • Predicted vs experimentally determined gene function • Evolutionary conservati ...
THE RESPIRATORY SYSTEM
THE RESPIRATORY SYSTEM

... and exhalation of gases (lungs)  Respiration: the exchange of gases by diffusion at the alveoli  Cellular Respiration: Use of oxygen by the mitochondria to ...
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Gene_Therapy

... Only effective way of addressing some genetic diseases ...
Fall 2014
Fall 2014

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Genomics of Food
Genomics of Food

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BioSc 231 Exam 4 2005

... _____ The fluctuation test of Luria and Delbruck (studying resistance to bacteriophge T1 infection) established that A. T1 phage was a mutagen. B. Mutations could arise prior to the time they were selected C. The mutation rate varies greatly from experiment to experiment. D. In E. coli the number of ...
Scientific Writing
Scientific Writing

... Advantages of DNA vaccines  Plasmids are easily manufactured in large amounts  DNA is very stable  DNA resists temperature extremes and so storage and transport are straight forward  A DNA sequence can be changed easily in the laboratory  can respond to changes in the infectious agent  By usi ...
DNA replication limits…
DNA replication limits…

... between different but non-tautomeric chemical forms of bases (e.g., bases with an extra proton, which can still bind but often with a mismatched nucleotide, such as an A with a G instead of a T) or between "normal" bases that nonetheless bond inappropriately (e.g., again, an A with a G instead of a ...
Targeting Cell Division Cycle 7 Kinase
Targeting Cell Division Cycle 7 Kinase

... forks to ensure proper restart after DNA repair (27). The pathway activated by replication blocks requires ATR and Chk1, which are important for determining cell fate upon such insults. Differently from other known DNA replication inhibitors, Cdc7 inhibition blocks DNA replication and induces apopto ...
CHAPTER 8 The Cellular Basis of Reproduction
CHAPTER 8 The Cellular Basis of Reproduction

... Environmental factors, such as cigarette smoke, air and water pollution, and exposure to ultraviolet radiation from the sun, are all known to damage the genes that control the cell ...
Unit 6: Inheritance
Unit 6: Inheritance

... – peas are genetically simple – most traits are controlled by single gene – each gene has only 2 versions • 1 completely dominant (A) (complete dominance) ...
Gene Disorders1(Saffen)
Gene Disorders1(Saffen)

... Example: Acondroplasia, the most common form of dwarfism, is caused by specific mutations in the fibroblast growth factor receptor subtype 3 gene (FGFR3), located at 4p16.3. Two mutations: 1138G>A (~98%) and 1138G>C (~1-2%) account for 99% of cases. These are gain-of-function mutations that change t ...
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Transformation

... If two mutants carrying a mutation of different genes combine to create a wild type function, two mutations compliment. ...
Genetic Mutations & Genetic Engineering
Genetic Mutations & Genetic Engineering

... Transformation: A cell takes in DNA from outside the cell Plasmid: Foreign DNA formed into a small circular DNA molecule. Used to incorporate foreign DNA into bacteria that will replicate allow it to be replicated Genetic Marker: Gene that makes it possible to distinguish bacteria that carry plasmid ...
Translational medicine: ribosomopathies
Translational medicine: ribosomopathies

... Here, Wong et al studied the sbds gene using an innovative model of genetically engineered amoeba, Dictyostelium dicoideum, a species that is distant from both yeast and mammals on the eukaryotic tree. The sbds gene is conserved in Dictyostelium, and conditional inactivation of the gene using temper ...
Biology 303 EXAM II 3/14/00 NAME
Biology 303 EXAM II 3/14/00 NAME

... operon, produces high amount of ß-galactosidase. What is a possible genotype of the cells? (I = lac repressor gene; Z, Y, A = lac operon structural genes; P = lac promoter; ...
gene
gene

... • Structural genes: encoding proteins • Regulatory genes: encoding products that interact with other sequences and affect the transcription and translation of these sequences • Regulatory elements: DNA sequences that are not transcribed but play a role in regulating other nucleotide sequences ...
Evolution and Differentiation
Evolution and Differentiation

... Of course, in multi-cellular organisms, cells do not spontaneously change their activity levels in the sense as above but what this experiment provides us with is additional support for viewing the cell as a non-linear dynamical system. If (virtually) all the cells have the same genes, how are they ...
PDF
PDF

... Endopolyploidy (increased cell ploidy) occurs during normal development in many eukaryotes. In higher plants, endopolyploidy is usually the result of endoreduplication – endonuclear DNA replication that produces chromosomes with multivalent chromatids. According to the ‘karyoplasmic ratio’ theory, a ...
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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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