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This document discusses different levels or "worlds" of learning and suggests families and schools should work together to support learning at each level, from early childhood through secondary and tertiary education. It asks what connects the systems of learning with real-world experiences and invites sharing stories on how to better join these two spheres.
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Affective Communication, Social and Biological Roots
Talk presented at the 9th Conference of the European Sociological Association.
Lisbon, Portugal, 2009
Biology DNA
1. DNA (deoxyribonucleic acid) is a chemical found in the nuclei of living cells that controls chemical changes and determines cell and organism type.
2. DNA is a long molecule composed of nucleotides, each containing a sugar (deoxyribose), phosphate group, and organic base (adenine, thymine, cytosine, or guanine).
3. DNA replicates before cell division by unwinding its double helix structure and using each strand as a template to make a new partner strand, resulting in two identical DNA molecules for each daughter cell after division.
Unit B5 6 Dna Replication
The document describes DNA replication and recombinant DNA. It discusses the three main steps of DNA replication: unzipping, complementary base pairing, and joining of adjacent nucleotides. Recombinant DNA is defined as DNA from two different organisms that is spliced together, and some of its main uses are listed, including producing hormones, proteins, vaccines, and developing pest/disease resistant crops. The document also provides an example of an anti-freeze gene being inserted into yeast to produce a protein added to ice cream to make it smoother.
62mutations2008
This document discusses different types of mutations including point mutations such as silent, missense, and nonsense mutations. It provides examples of genetic diseases caused by specific mutations, such as sickle cell anemia which results from a missense mutation and cystic fibrosis which involves a deletion mutation. The document notes that mutations can occur through single base changes, frameshifts, insertions or deletions and discusses how these mutations can impact protein function and cause disease.
Biology 12 - DNA Mutations and Expression
This document summarizes sections 4.4 and 4.5 of a chapter on DNA structure and gene expression. Section 4.4 discusses how gene mutations, including point mutations and frameshift mutations, can occur from errors in DNA replication or exposure to mutagens. These mutations can cause cancer if they accumulate over time and disrupt cell regulation and programmed cell death. Section 4.5 describes techniques for gene cloning, including using restriction enzymes to insert genes into vectors, bacterial replication of recombinant DNA, and the polymerase chain reaction to amplify specific DNA sequences.
Revised Bio 1wfx Recombinant D N A
The document discusses recombinant DNA technology and the Human Genome Project. Some key points:
- The Human Genome Project, started in 1990 and completed in 2003, mapped the entire human genome sequence to further understand human genetics and hereditary disease.
- Recombinant DNA technology allows DNA from one organism to be cut and combined with DNA from another, and is used to produce medicines like human insulin in bacteria.
- Understanding an individual's genetic makeup through projects like the Human Genome Project could help develop personalized medicines tailored to each person's genetics.
- Nutrigenomics studies how different foods may affect gene expression and disease risk depending on a person's genetics. Understanding these interactions could help prevent chronic diseases.
10 Lecture Ppt
The document summarizes key concepts about DNA and genetics, including:
1) DNA was identified as the genetic material through experiments showing it could be transferred between bacteria to cause heritable changes.
2) DNA and RNA are polymers composed of nucleotides containing nitrogenous bases, phosphate groups, and a pentose sugar.
3) DNA replication is semiconservative and involves unwinding the DNA double helix, adding complementary nucleotides, and rejoining to form two new DNA molecules.
4) Genes specify the sequence of amino acids in proteins through transcription of DNA to mRNA and translation of mRNA to proteins with the help of tRNA and ribosomes.
DNA Structure and Replication - Section 4-1 and 4-2
This document summarizes key sections from a textbook chapter on DNA structure and gene expression. It describes decades of research that established DNA as the genetic material, including Griffith's experiments showing a transforming substance in bacteria and Avery's experiments identifying the substance as DNA. It also summarizes Hershey and Chase's experiments using radioactive viruses that demonstrated DNA enters bacterial cells during infection. The chapter then describes the double-helix structure of DNA and the semiconservative process of DNA replication, in which each new DNA molecule contains one original and one newly synthesized strand. Key replication enzymes such as DNA polymerase and ligase are also summarized.
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Affective Communication, Social and Biological Roots
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1. DNA (deoxyribonucleic acid) is a chemical found in the nuclei of living cells that controls chemical changes and determines cell and organism type.
2. DNA is a long molecule composed of nucleotides, each containing a sugar (deoxyribose), phosphate group, and organic base (adenine, thymine, cytosine, or guanine).
3. DNA replicates before cell division by unwinding its double helix structure and using each strand as a template to make a new partner strand, resulting in two identical DNA molecules for each daughter cell after division.
Unit B5 6 Dna Replication
The document describes DNA replication and recombinant DNA. It discusses the three main steps of DNA replication: unzipping, complementary base pairing, and joining of adjacent nucleotides. Recombinant DNA is defined as DNA from two different organisms that is spliced together, and some of its main uses are listed, including producing hormones, proteins, vaccines, and developing pest/disease resistant crops. The document also provides an example of an anti-freeze gene being inserted into yeast to produce a protein added to ice cream to make it smoother.
62mutations2008
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Biology 12 - DNA Mutations and Expression
This document summarizes sections 4.4 and 4.5 of a chapter on DNA structure and gene expression. Section 4.4 discusses how gene mutations, including point mutations and frameshift mutations, can occur from errors in DNA replication or exposure to mutagens. These mutations can cause cancer if they accumulate over time and disrupt cell regulation and programmed cell death. Section 4.5 describes techniques for gene cloning, including using restriction enzymes to insert genes into vectors, bacterial replication of recombinant DNA, and the polymerase chain reaction to amplify specific DNA sequences.
Revised Bio 1wfx Recombinant D N A
The document discusses recombinant DNA technology and the Human Genome Project. Some key points:
- The Human Genome Project, started in 1990 and completed in 2003, mapped the entire human genome sequence to further understand human genetics and hereditary disease.
- Recombinant DNA technology allows DNA from one organism to be cut and combined with DNA from another, and is used to produce medicines like human insulin in bacteria.
- Understanding an individual's genetic makeup through projects like the Human Genome Project could help develop personalized medicines tailored to each person's genetics.
- Nutrigenomics studies how different foods may affect gene expression and disease risk depending on a person's genetics. Understanding these interactions could help prevent chronic diseases.
10 Lecture Ppt
The document summarizes key concepts about DNA and genetics, including:
1) DNA was identified as the genetic material through experiments showing it could be transferred between bacteria to cause heritable changes.
2) DNA and RNA are polymers composed of nucleotides containing nitrogenous bases, phosphate groups, and a pentose sugar.
3) DNA replication is semiconservative and involves unwinding the DNA double helix, adding complementary nucleotides, and rejoining to form two new DNA molecules.
4) Genes specify the sequence of amino acids in proteins through transcription of DNA to mRNA and translation of mRNA to proteins with the help of tRNA and ribosomes.
DNA Structure and Replication - Section 4-1 and 4-2
This document summarizes key sections from a textbook chapter on DNA structure and gene expression. It describes decades of research that established DNA as the genetic material, including Griffith's experiments showing a transforming substance in bacteria and Avery's experiments identifying the substance as DNA. It also summarizes Hershey and Chase's experiments using radioactive viruses that demonstrated DNA enters bacterial cells during infection. The chapter then describes the double-helix structure of DNA and the semiconservative process of DNA replication, in which each new DNA molecule contains one original and one newly synthesized strand. Key replication enzymes such as DNA polymerase and ligase are also summarized.
Mutation
Mutations are any changes in the DNA sequence of an organism. They can be caused spontaneously during DNA replication or repair, or can be induced by mutagens like chemicals, radiation, or viruses. Mutations are classified as point mutations, which change a single DNA base, or frameshift mutations, which insert or delete DNA bases. Cells have DNA repair mechanisms to correct mutations, such as base excision repair, nucleotide excision repair, and mismatch repair. Unrepaired mutations can be harmful, beneficial, or have no effect on the organism.
Central Dogma Of Dna
The document describes the central dogma of molecular biology, which is the flow of genetic information from DNA to RNA to proteins. It covers DNA replication, transcription, translation, and how mutations can occur during these processes. DNA replication is semi-conservative and produces two identical DNA molecules from one original. Transcription produces mRNA from DNA, and translation uses mRNA to produce proteins according to the genetic code. Mutations can occur during replication, transcription or translation and result in changes to the amino acid sequence or reading frame of proteins.
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This document discusses different types of mutations that can occur in DNA, including base changes, insertions/deletions of bases, frameshift mutations, and trinucleotide repeats. It provides examples of different mutations that cause conditions like sickle cell anemia, beta-thalassemia, Huntington's disease, and retinoblastoma. The key points are that mutations can be random changes to DNA that provide raw material for evolution, and they can occur in germ cells or somatic cells with different effects on inheritance and disease.
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Breast cancer develops from breast tissue and is one of the most common types of cancer in women. Some signs and symptoms include a lump in the breast, changes to the skin on the breast, or fluid coming from the nipple. Risk factors include female sex, older age, family history and certain genetic mutations. Diagnosis involves exams, mammograms, and other scans. Treatment options include surgery to remove tumors, medication like chemotherapy or hormone therapy, and radiation therapy.
Gene mutations ppt
Gene mutations can occur when there is a change in the DNA code, such as a substitution, insertion, or deletion of nucleotide bases. Substitution mutations, where one base is swapped for another, typically have the smallest effect since only one amino acid may change. Insertion and deletion mutations, which add or remove bases, can have larger effects by disrupting the reading frame of the entire DNA sequence. An example is sickle cell anemia, a substitution mutation that causes red blood cells to take on a sickle shape.
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