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Identification of rare cancer driver mutations by network reconstruction
Identification of rare cancer driver mutations by network reconstruction

... • The aim is to find which specific gene and/or mutation is contributing to tumorigenesis in addition to the acknowledged cancer associated gene. Thus, new drug targets may be found. • Exons sequencing for mutations • SNP chip for detecting deletion and amplification • SAGE for expression, for confi ...
Molecular Genetics
Molecular Genetics

... 3.B.1 Cells can be activated, produce new products, and retain their activated state through gene regulation. 3.B.2 A variety of intercellular and intracellular signal transmissions mediate gene expression 3.C.1 Changes in genotype can result in changes in phenotype. 3.C.2 Biological systems possess ...
QUIZ 4on ch12.doc
QUIZ 4on ch12.doc

... 5. The Law of Segregation (Mendel) is best demonstrated using: a. a monohybrid cross. b. a dihybrid cross c. a testcross. d. a back cross. e. two recessive varieties of the gene under study. ...
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*J5JT*_§JJU: ~$f4~*

... What is the term for metabolic pathways that release stored energy by breaking down complex ...
Biology 30 Patterns and Probabilities
Biology 30 Patterns and Probabilities

... exchange pieces of chromosomes. This is a random event and can occur anywhere along a sister chromatid, except near the centromere. Suppose you are studying two genes and crossing over occurs between them then the alleles will end up on separate chromosomes and will therefore migrate into different ...
Wednesday, September 5
Wednesday, September 5

... means to process RNA transcripts, and even if the need for RNA processing is avoided by using cDNA, bacteria lack enzymes to catalyze the post-translational processing that many human proteins undergo. ...
DNA - eduBuzz.org
DNA - eduBuzz.org

... The genetic information contained within the DNA can be thought of as a list of genetic instructions that the cells uses to make proteins. Proteins are made from amino acids joined together into chains. There are 20 different types of amino acids and the differences between proteins are due to the a ...
Learning Goals Chapter 13
Learning Goals Chapter 13

... 2. Explain how a point mutation occurs and give a common example. 3. Explain how a frameshift mutation occurs and give a common example. 4. Describe the four types of chromosomal mutations: Deletion Duplication Inversion Translocation 5. Describe how errors in disjunction occur and give examples. 6. ...
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NTNU brevmal

... a) Two labrador retriever dogs are mated. Both are black and heterozygous for the black (B) and brown (b) alleles at the gene for coat colour (i.e. both parents are Bb). Use Mendel’s first law and a Punnett square to explain what ratio of black and brown puppies we expect from this mating. (35%) b) ...
microbio 40 [4-20
microbio 40 [4-20

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Genetic Modification Regulations and Procedures
Genetic Modification Regulations and Procedures

... Double helix cell ...
Quantitative PCR
Quantitative PCR

... • A method that allows to follow in real time (that is why is also called Real-Time PCR) the amplification of a target. • The target can be nucleic acids (RNA or DNA). • Taq polymerase can only synthesize DNA, so how do we study RNA using qPCR? ...
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Prentice Hall Biology
Prentice Hall Biology

... • Cystic fibrosis – caused by the deletion of three bases in the DNA of the gene resulting in an amino acid (phenylalanine) missing from the protein. The protein produced by the gene is a chloride ion pump. The deletion of phenylalanine prevents the protein from being transported to the cell membran ...
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Evolutionary change in proteins 2

... 1. The phenotype is determined by the proteome & transcriptome. 2. Selection acts on the phenotype, and is blind to the genotype. Therefore: two species/individuals that have different forms of a protein will be selected differently - even if the genes DNA sequence is identical. DNA ...
flashBAC - 2BScientific
flashBAC - 2BScientific

... • Baculovirus vectors also used to transduce mammalian cells to express genes under (eg.) CMV promoter – The virus does not replicate in any mammalian cells ...
Chapter 4 - Modern GENETICS
Chapter 4 - Modern GENETICS

... generation to generation in humans. ...
Genetics Slides - The Adapa Project
Genetics Slides - The Adapa Project

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Control & Regulation
Control & Regulation

... of valuable resources.  Humans contain a huge number of genes (around 30,000) which are affected by many internal and external factors which interact with each other in a complex way which is not yet fully understood.  Cancer cells are cells which are permanently switched on to carry out growth an ...
LECTURE 31 1. A few definitions: Cancer: Unregulated cell growth
LECTURE 31 1. A few definitions: Cancer: Unregulated cell growth

... Cells do not detach from tumor and invade surrounding tissues ...
X Chromosome
X Chromosome

... • The expression of genes on the sex chromosomes differs from the expression of autosomal genes. • Genes located on the sex chromosomes are called sex- linked genes or X-linked genes. • Males express all of the alleles on both sex chromosomes. • In females one of the two X chromosomes is randomly tu ...
chromosome Y
chromosome Y

... daughters inherit defect from the disabled father mother vector tranfers the disease on her sons = cross inheritance typical for genes fully connected with sex noticeable difference in the frequency of illnesses between the sex > much more common by the individuals of type XY than XX genes localized ...
Chapter 13 PowerPoint.ppt
Chapter 13 PowerPoint.ppt

... from the sex chromosomes even though females have 2 X chromosomes and males have only 1 • In each female cell, 1 X chromosome is inactivated and is highly condensed into a Barr body • Females heterozygous for genes on the X chromosome are genetic mosaics ...
Chapter 13 PowerPoint
Chapter 13 PowerPoint

... from the sex chromosomes even though females have 2 X chromosomes and males have only 1 • In each female cell, 1 X chromosome is inactivated and is highly condensed into a Barr body • Females heterozygous for genes on the X chromosome are genetic mosaics ...
16-1 Genes and Variation - Lincoln Park High School
16-1 Genes and Variation - Lincoln Park High School

... alleles there are many different phenotypes that can ...
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Epigenetics of human development

Development before birth, including gametogenesis, embryogenesis, and fetal development, is the process of body development from the gametes are formed to eventually combine into a zygote to when the fully developed organism exits the uterus. Epigenetic processes are vital to fetal development due to the need to differentiate from a single cell to a variety of cell types that are arranged in such a way to produce cohesive tissues, organs, and systems.Epigenetic modifications such as methylation of CpGs (a dinucleotide composed of a 2'-deoxycytosine and a 2' deoxyguanosine) and histone tail modifications allow activation or repression of certain genes within a cell, in order to create cell memory either in favor of using a gene or not using a gene. These modifications can either originate from the parental DNA, or can be added to the gene by various proteins and can contribute to differentiation. Processes that alter the epigenetic profile of a gene include production of activating or repressing protein complexes, usage of non-coding RNAs to guide proteins capable of modification, and the proliferation of a signal by having protein complexes attract either another protein complex or more DNA in order to modify other locations in the gene.
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