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The PTCH gene and Gorlin Syndrome
The PTCH gene and Gorlin Syndrome

... ► The PTCH gene is sequenced ► The results are reported to the referring physician/genetic counselor ...
14-1 Human Heredity
14-1 Human Heredity

... 9. What does “polygenic” mean? ________________________________________________ 10. What environmental factor has improved the height of Americans? __________________________ 11. Our complete set of genetic information is called The _________________ ___________________ 12. Compared to peas and frui ...
IARC study identifies new genetic factors linked to HPV
IARC study identifies new genetic factors linked to HPV

Haploid (__)
Haploid (__)

... Human genetic traits In humans there are ____chromosomes= __________genes there are problems in studying human genes ...
Name____________________________ DNA Investigation
Name____________________________ DNA Investigation

Cancer without disease
Cancer without disease

... of cancer cells, also known as in also noted. These examples suggest situ tumours. It has been estimated that either an increase or decrease that more than one-third of in the angiogenic defence can alter women aged 40 to 50, who did the rate of cancer progression. not have cancer-related disease in ...
Concept 20.1 A. -Plasmid is the cloning vector.
Concept 20.1 A. -Plasmid is the cloning vector.

... b) Presence of introns (non-coding regions), in most Eukaryotic genes. These make it hard to correct expression of the gene by bacteria, as they do not have RNA splicing machinery. - Use a cDNA form of the gene which only includes the exons of the gene. -Bacteria can express a eukaryotic cDNA gene i ...
ludwig institiute for cancer research and powdermed initiate a phase
ludwig institiute for cancer research and powdermed initiate a phase

... Oxford, UK, 17th September 2004 – PowderMed Ltd (PowderMed), a company focusing on the development of therapeutic DNA vaccines, in collaboration with its partner, the Ludwig Institute for Cancer Research (LICR), have announced that they have initiated a Phase I trial of a novel therapeutic DNA cance ...
Mutations—1 [1] Mutations [2] To understand what mutations are
Mutations—1 [1] Mutations [2] To understand what mutations are

... continually makes new cells for routine growth and repair. / The other kind is called meiosis, which happens during the process of reproduction. / Meiosis forms sperm and egg cells, which enable an organism to reproduce offspring. [3] Just before mitosis, a cell—called the parent cell—makes a copy o ...
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Chapter 18 notes

... b} other proteins may bend DNA bringing enhancer closer to promoter c} proteins binding at enhancer interact with RNA pol to initiate transcription. d} repressors may block RNA pol or ...
Genetics Review Sheet
Genetics Review Sheet

... In what ways do mutations occur in a cell? There are many ways. Some examples are during DNA Replication, when DNA is copying itself. Maybe it skips a pair of nitrogen base pairs, or one mismatches, maybe a group of base pairs is added out of no where (wasn’t in original DNA). A mutation is a change ...
Chapter 14 Outline
Chapter 14 Outline

4D-THE GENETICS OF CANCER.key
4D-THE GENETICS OF CANCER.key

... referred to as antioncogenes. This term was considered inappropriate since they do not oppose the action of the oncogenes and are more correctly known as tumor suppressor genes. The paradigm for our understanding of the biology of tumor suppressor genes is the eye tumor retinoblastoma. It is importa ...
Assay for Methylation of genes
Assay for Methylation of genes

mutations[1]
mutations[1]

... they are faulty, mutation rates will be elevated.  Some mutations increase the overall rate of mutation at other genes; these mutations usually occur in genes that encode components of the replication machinery or DNA repair enzymes. ...
Genetics I
Genetics I

... 9. Section of a chromosome __gene___________________________________ 10. Gene that keeps other genes from showing trait ___dominant_____________ 11. Recessive gene __genes that do not show traits in presence of dominant gene 12. Heterozygous _has a dominant and recessive gene for a trait_____ 13. Me ...
Othon Iliopoulos, MD Associate Professor of Medicine, Harvard
Othon Iliopoulos, MD Associate Professor of Medicine, Harvard

... discovered are “active” and they reverse the consequences of VHL protein loss. They are therefore very promising agents for targeting cancer angiogenesis. 2) Targeting the metabolic reprogramming of RCC and HIF2a expressing tumors for therapy My laboratory provided significant insights into how HIF2 ...
Othon Iliopoulos, MD Associate Professor of Medicine, Harvard
Othon Iliopoulos, MD Associate Professor of Medicine, Harvard

... discovered are “active” and they reverse the consequences of VHL protein loss. They are therefore very promising agents for targeting cancer angiogenesis. 2) Targeting the metabolic reprogramming of RCC and HIF2a expressing tumors for therapy My laboratory provided significant insights into how HIF2 ...
Intro to Genetics
Intro to Genetics

... Try some examples on the board: BB x bb and Bb x bb ...
Unit I: Genes, Nucleic A...d Chromosomes - BioWiki
Unit I: Genes, Nucleic A...d Chromosomes - BioWiki

computational biology
computational biology

... how it looks, how it behaves, and its physiology. So a change in an organism's DNA can cause changes in all aspects of its life. Mutations are essential to evolution; they are the raw material of genetic variation. Without mutation, evolution could not occur. In this lab we will explore these key qu ...
Epigenetics - HudsonAlpha Institute for Biotechnology
Epigenetics - HudsonAlpha Institute for Biotechnology

... cells of living creatures contain millions of methyl tags, working as switchboard operators to control which genes are active and which are silenced. Methyl groups represent just one of the epigenetic mechanisms cells use to oversee gene activity. These mechanisms account for the very specific patte ...
Overview of Articles for the literature talks Nr PMID Titel Date
Overview of Articles for the literature talks Nr PMID Titel Date

... The human genome encodes the blueprint of life, but the function of the vast majority of its nearly three billion bases is unknown. The Encyclopedia of DNA Elements (ENCODE) project has systematically mapped regions of transcription, transcription factor association, chromatin structure and histone ...
DNA Replication
DNA Replication

... – Mutation can occur in a growth-factor gene, causing rapid, uncontrolled cell growth – Error in DNA replication, producing multiple copies of a single-growth factor gene – Change in gene’s location--falls under the control of a different promoter is transcribed more often (producing more growth-fac ...
Overview of Articles for the literature talks Nr PMID Titel Date
Overview of Articles for the literature talks Nr PMID Titel Date

... The human genome encodes the blueprint of life, but the function of the vast majority of its nearly three billion bases is unknown. The Encyclopedia of DNA Elements (ENCODE) project has systematically mapped regions of transcription, transcription factor association, chromatin structure and histone ...
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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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