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The Question of Questions: What is a Gene? Comments on Rolston
The Question of Questions: What is a Gene? Comments on Rolston

... breast cancer, or the gene for blue eyes, or the gene for Marfan syndrome) would count as a Gene-P. Gene-D by contrast is the sense of a gene when it is defined by a nucleic acid sequence that provides the template resource (or information) for some set of potential downstream polypeptide and/or RNA ...
genetically
genetically

... Haploid: a single set of chromosomes (half the full set of genetic material). Present in the egg and sperm cells of animals and in the egg and pollen cells of plants. Human beings have 23 chromosomes in their reproductive cells. Diploid: a full set of genetic material, consisting of paired chromosom ...
PEDIGREE STUDIES
PEDIGREE STUDIES

... Therefore, persons I-1 and II-2 have ee genotypes. They are the only two individuals who are homozygous recessive and show the recessive trait. They have attached earlobes. All unshaded symbols represent individuals who have at least one dominant gene (they are either homozygous dominant EE or heter ...
Shining a (UV) light on the regulatory dark matter of bacteria
Shining a (UV) light on the regulatory dark matter of bacteria

... E-CLASH, for sequencing ncRNAs-mRNA pairs captured in vivo. We demonstrate that RNase E-CLASH is able to profile the ncRNA-interactome providing high-throughtput functional data for hundreds of known and novel ncRNAs. Using this data we demonstrate that the ncRNA (Esr41), transcribed by the human en ...
Genomes and SNPs in Malaria and Sickle Cell Anemia
Genomes and SNPs in Malaria and Sickle Cell Anemia

... into mRNA transcripts. U (Uracil) substitutes T in mRNA. mRNA translation machinery produces proteins. Proteins are made of amino acids. One amino acid is encoded by three nucleotides. Sequence Variation DNA sequence can differ between individuals. Differences can be mutations of single nucleotides ...
Legends for Supplementary Materials Figure S1. Schematic
Legends for Supplementary Materials Figure S1. Schematic

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Limb Development: Hox Genes
Limb Development: Hox Genes

... Development 126: 2589-2596). For an excellent review of the development of the vertebrate heart see Fishman and Chien, 1997. Development 124: 2099-2117. While retinoic acid has specific effects on limb development, the general concensus is that it is not a true morphogen in the development of the ma ...
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H-W equilforces

... not be surprised if we ended up with more of one color than the other, or if by chance we got 7 white and 3 black beans. In genetics, to get to the next generation, we would next draw from a bowl that had 70% white and 30 % black beans, rather than the 50:50 split we started with. Then it would not ...
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The Genetics

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background objective materials and methods results conclusions

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Homework 6 - public.iastate.edu
Homework 6 - public.iastate.edu

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...  The BMP levels appear to be used throughout the animal kingdom to specifiy dorsal ventral axis. In sea anemone embryo the Bmp4 and Dpp ortholog is expressed asymmetrically at the edge of the blastopore (A).  The Wnt and Hox genes are used to specify A-P axis throughout all bilaterans. The Hox gen ...
Gene Section RECQL4 (RecQ protein-like 4) Atlas of Genetics and Cytogenetics
Gene Section RECQL4 (RecQ protein-like 4) Atlas of Genetics and Cytogenetics

... helicases and contains from aa 476 to 824 an helicase domain with a potential ATP binding site from aa 502 to 509, and the DEAH box from aa 605 to 608. ...
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Unifactorial or single gene disorders

... A family tree is a shorthand system of recording information about a family. It usually begins with the person through whom the family came to the attention of the investigator. This person is referred to as the index case, proband or propositus, or if female, the proposita. The position of the prob ...
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Unifactorial or single gene disorders

... a risk of 50% of passing the condition to his son and daughter in each pregnancy. A couple with a boy affected by an autosomal recessive condition has a 25% chance to have another affected child with each pregnancy Molecular diagnosis are important diagnostic tools for single gene disorders and they ...
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Familial Lipoprotein Lipase Deficiency

... Approximately a quarter of affected children show signs before the age of one year, and the majority develop symptoms before 10, but some women only show symptoms during pregnancy. Because this condition is so rare, it is possible that people with LPLD may not be formally diagnosed until adulthood. ...
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HW_CH12-Biol1406.doc

... 8. Anne Boleyn, King Henry VIII's second wife, was beheaded because she did not provide him with a son as an heir. Explain why King Henry should have blamed himself and not his wife. a. All of the sperm that males produce contain an X chromosome, so their genetic contribution to the child determines ...
Section 3 - Applying statistical Tests to Microarray Data
Section 3 - Applying statistical Tests to Microarray Data

... • Can apply T test to work out if the mean of data is same or different between two conditions. • Can apply ANOVA to work out if the mean of data is same or different across two or more conditions. • There are several issues to consider before applying these statistical “filtering” techniques eg. – ...
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Gene nomenclature

Gene nomenclature is the scientific naming of genes, the units of heredity in living organisms. An international committee published recommendations for genetic symbols and nomenclature in 1957. The need to develop formal guidelines for human gene names and symbols was recognized in the 1960s and full guidelines were issued in 1979 (Edinburgh Human Genome Meeting). Several other species-specific research communities (e.g., Drosophila, mouse) have adopted nomenclature standards, as well, and have published them on the relevant model organism websites and in scientific journals, including the Trends in Genetics Genetic Nomenclature Guide. Scientists familiar with a particular gene family may work together to revise the nomenclature for the entire set of genes when new information becomes available. For many genes and their corresponding proteins, an assortment of alternate names is in use across the scientific literature and public biological databases, posing a challenge to effective organization and exchange of biological information. Standardization of nomenclature thus tries to achieve the benefits of vocabulary control and bibliographic control, although adherence is voluntary. The advent of the information age has brought gene ontology, which in some ways is a next step of gene nomenclature, because it aims to unify the representation of gene and gene product attributes across all species.Gene nomenclature and protein nomenclature are not separate endeavors; they are aspects of the same whole. Any name or symbol used for a protein can potentially also be used for the gene that encodes it, and vice versa. But owing to the nature of how science has developed (with knowledge being uncovered bit by bit over decades), proteins and their corresponding genes have not always been discovered simultaneously (and not always physiologically understood when discovered), which is the largest reason why protein and gene names do not always match, or why scientists tend to favor one symbol or name for the protein and another for the gene. Another reason is that many of the mechanisms of life are the same or very similar across species, genera, orders, and phyla, so that a given protein may be produced in many kinds of organisms; and thus scientists naturally often use the same symbol and name for a given protein in one species (for example, mice) as in another species (for example, humans). Regarding the first duality (same symbol and name for gene or protein), the context usually makes the sense clear to scientific readers, and the nomenclatural systems also provide for some specificity by using italic for a symbol when the gene is meant and plain (roman) for when the protein is meant. Regarding the second duality (a given protein is endogenous in many kinds of organisms), the nomenclatural systems also provide for at least human-versus-nonhuman specificity by using different capitalization, although scientists often ignore this distinction, given that it is often biologically irrelevant.Also owing to the nature of how scientific knowledge has unfolded, proteins and their corresponding genes often have several names and symbols that are synonymous. Some of the earlier ones may be deprecated in favor of newer ones, although such deprecation is voluntary. Some older names and symbols live on simply because they have been widely used in the scientific literature (including before the newer ones were coined) and are well established among users.
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