• Study Resource
  • Explore
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
Gene Section CDA (Cytidine Deaminase)  Atlas of Genetics and Cytogenetics
Gene Section CDA (Cytidine Deaminase) Atlas of Genetics and Cytogenetics

... in the human CDA gene (Yue et al., 2003). Ethnic differences in the minor allele frequencies of these variations have been reported. The 79A>C (Lys27Gln) was found at 0.30-0.36 frequencies in Caucasians, at 0.20-0.21 in Japanese and at 0.04-0.10 in Africans (Ueno et al., 2007). In contrast, the 208G ...
Single gene disorders
Single gene disorders

Gene Section SLIT2 (slit homolog 2 (Drosophila)) Atlas of Genetics and Cytogenetics
Gene Section SLIT2 (slit homolog 2 (Drosophila)) Atlas of Genetics and Cytogenetics

... repellent for ROBO-expressing axons (Brose et al., 1999; Kidd et al., 1999; Long et al., 2004). Outside the CNS, SLIT plays an important role during embryonic development and in human pathology. Neuronal guidance: SLIT proteins function as chemorepellents throughout the central nervous system to res ...
DNA MUTATIONS AND THEIR REPAIR
DNA MUTATIONS AND THEIR REPAIR

Chapter 12
Chapter 12

... Sex chromosomes are nonidentical but still homologous Homologous chromosomes interact, then segregate from one another during meiosis ...
Zhang-worms
Zhang-worms

... and gaps by X-ray, 12C, and 18Ar-ion beam irradiation. (3) A checkpoint kinase Ce-atl-1 (ATM/ATR like 1) was also involved in repair for X-ray and UV damages of mitotic and meiotic cells. ...
Cancer Prone Disease Section Cowden disease Atlas of Genetics and Cytogenetics
Cancer Prone Disease Section Cowden disease Atlas of Genetics and Cytogenetics

... signal cell pathway by dephosphorylating PIP3. Mutations Germinal: To date, at least 110 mutations have been described; they are observed along the various exons of the gene except the 9th (never described) and the 1st (very few reports); a mutational hot spot is observed in exon 5 in relation with ...
Metabolic Activation of 4-Ipomeanol by
Metabolic Activation of 4-Ipomeanol by

... 4-Ipomeanol has been considered as an agent for lung cancer olites (Table 2). The specific binding of 4-ipomeanol metabo therapy (5). However, since this compound requires metabolic activation for its cell-killing effect the species differences in Plites demonstrated with rabbit CYP4B1 equals 84 dpm ...
CRISPR-Cas Gene Editing to Cure Serious Diseases: Treat the
CRISPR-Cas Gene Editing to Cure Serious Diseases: Treat the

... immediate need, for therapeutic purposes, in editing or correcting the DNA. It is also more appropriate to apply a new technology like CRISPR-Cas9 in the setting in which the consequences of the therapy are directed only to the patient and are not passed on to or altering the gene pool for future ge ...
Distinguishing endogenous versus exogenous DNA
Distinguishing endogenous versus exogenous DNA

... In the late 1990s it was reported that human DNA existed on the Shroud of Turin, and although in a generally degraded state, certain regions were sufficiently intact to clone and sequence three genes from bloodstained fibers: human betaglobin, amelogenin X and amelogenin Y. An unknown variable in su ...
File
File

... Too much time in the tanning booth might damage epithelial cells due to the UV radiation. the mosty likely effect would be….. ...
Genetic Disorders
Genetic Disorders

... whose concepts and approaches are important components of ...
Lung Cancer and the ALK S1206Y Mutation This material will help
Lung Cancer and the ALK S1206Y Mutation This material will help

... Lung Cancer and the ALK S1206Y Mutation This material will help you understand: • the basics of lung cancer
 • the role of the ALK gene in lung cancer • if there are any drugs that might work better if you have certain changes in the ALK gene What is lung cancer? Lung cancer is a type of cancer that ...
Lung Cancer and the ALK G1269A Mutation This material will help
Lung Cancer and the ALK G1269A Mutation This material will help

... Lung Cancer and the ALK G1269A Mutation This material will help you understand: • the basics of lung cancer
 • the role of the ALK gene in lung cancer • if there are any drugs that might work better if you have certain changes in the ALK gene What is lung cancer? Lung cancer is a type of cancer that ...
Lung Cancer and the ALK L1196M Mutation This material will help
Lung Cancer and the ALK L1196M Mutation This material will help

... Lung Cancer and the ALK L1196M Mutation This material will help you understand: • the basics of lung cancer
 • the role of the ALK gene in lung cancer • if there are any drugs that might work better if you have certain changes in the ALK gene What is lung cancer? Lung cancer is a type of cancer that ...
Chapter 15
Chapter 15

... from the fertilization of gametes in which nondisjunction occurred = abnormal number of a particular chromosome   A monosomic zygote has only one copy of a particular chromosome   A trisomic zygote has three copies of a particular chromosome ...
Cells and DNA Table of Contents
Cells and DNA Table of Contents

... For more information about chromosomes: Genetics Home Reference provides information about each human chromosome (http://ghr.nlm.nih.gov/chromosomes) written in lay language. The Centre for Genetics Education offers a fact sheet that introduces genes and chromosomes (http://www.genetics.edu.au/Info ...
here
here

... Evolution occurs within populations where the fittest organisms have a selective advantage. Over time the advantages genes become fixed in a population and the population gradually changes. Note: this is not in contradiction to the the theory of neutral evolution. (which says what ?) Processes that ...
Pharmacogenetics
Pharmacogenetics

... about half of them would be DPD deficient. It’s one of the causes for toxicity of 5-FU, but it’s not the only cause. The other cause is unknown. b. This observation is similar to warfarin. XXIX. DPD DEFICIENCY [S29] a. DPD deficient individual are phenotypically normal. The drug just can’t be cleare ...
Answers to End-of-Chapter Questions – Brooker et al ARIS site
Answers to End-of-Chapter Questions – Brooker et al ARIS site

Genetic Testing for Hereditary Breast and/or Ovarian Cancer
Genetic Testing for Hereditary Breast and/or Ovarian Cancer

Analysis of genetic systems using experimental evolution and whole
Analysis of genetic systems using experimental evolution and whole

Douillard found that Flik
Douillard found that Flik

... in 2009 about the Flik gene of H. pylori • Statistical data was gathered to determine which genes in this experiment underwent the greatest changes • GenMAPP was used to determine the most upregulated and downregulated genes • MAPPFinder indicated that many of the top 10 most significant genes dealt ...
Dana Neel - Tay Sachs
Dana Neel - Tay Sachs

... •  Appearance of aforementioned symptoms •  “Cherry-red” spot on eyes, caused by lipid-laden ganglion cells •  Larger startle reflex to noise •  Before 1970, Tay-Sachs could not be diagnosed at birth ...
Biochemistry 6: Model Organisms
Biochemistry 6: Model Organisms

... Transmission genetics is the general process by which traits controlled by factors (genes) are transmitted through gametes from generation to generation. Its fundamental principles were first put forward by Gregor Mendel in the midnineteenth century. Later work by others showed that genes are on chr ...
< 1 ... 219 220 221 222 223 224 225 226 227 ... 504 >

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.
  • studyres.com © 2025
  • DMCA
  • Privacy
  • Terms
  • Report