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... from larval to pupal stages, but once a certain size or weight – the critical weight – is reached, development proceeds independently of nutrition. What regulates this switch? On p. 2345, Christen Mirth and colleagues report that in Drosophila wing imaginal discs, it is ecdysone molting hormone sign ...
Mendelian Genetics
Mendelian Genetics

... • Law of Segregation: two alleles for a gene will separate during meiosis ...
Comparing DNA Sequences to Understand Evolutionary
Comparing DNA Sequences to Understand Evolutionary

... Between 1990–2003, scientists working on an international research project known as the Human Genome Project were able to identify and map the 20,000–25,000 genes that define a human being. The project also successfully mapped the genomes of other species, including the fruit fly, mouse, and Escheri ...
BIOINFORMATICS AND GENE DISCOVERY
BIOINFORMATICS AND GENE DISCOVERY

... •interconnected assembly of simple processing elements (units or nodes) •nodes functionality is similar to that of the animal neuron •processing ability is stored in the inter-unit connection strengths (weights) •weights are obtained by a process of adaptation to, or learning from, a set of training ...
The Gene Concept - bioinf.uni
The Gene Concept - bioinf.uni

... “A gene is a database entry with an Ensembl gene ID.” a computer scientist “A gene is what Wikipedia says it is.” a student “A gene is a locatable region of genomic sequence, corresponding to a unit of inheritance, which is associated with regulatory regions, transcribed regions and/or other functio ...
Horizontal and Vertical Gene Transfer
Horizontal and Vertical Gene Transfer

... eukaryocytes in the same way as bacterial mobile elements. In vitro, genes to confer functions can be introduced into eukaryocytes by transfection or conjugation. Retrovirus infection or hepatitis B virus infection transfers the viral genes to the chromosome of the host. These are examples of horizo ...
BiochemLecture03
BiochemLecture03

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Review for Heredity Unit

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Regulation of Bovine Parathyroid Hormone (Pth) Gene Expression

... processes involved in the establishment and maintenance or h a reactivation occurs. h i s of latency investigation has established an in U model using genetic manipulation of a mutant of HSV type 1, h i 8 1 4 which has a mutation in VMW65, a protein responsible for the transactivation of iuumdiate e ...
BioInformatics (1)
BioInformatics (1)

... Exons to gene (without cDNA or homolog) ~30% [Laub 98] Gene to regulation ~10% [Hughes 00] Regulated gene to protein sequence 98% [Gesteland ] Sequence to secondary-structure (,b,c) 77% [CASP] Secondary-structure to 3D structure 25% [CASP] 3D structure to ligand specificity ~10% [Johnson 99] ...
Regulation of Gene Activity in Eukaryotes
Regulation of Gene Activity in Eukaryotes

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... distributed on the tree of life, and does not reflect the diversity accordingly either. ...
Mendelian Genetics
Mendelian Genetics

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No Slide Title
No Slide Title

... ...while attempting to do anti-sense KO of gene expression in C. elegans, Guo and Kemphues, Cell 81, 611 (1995) observed that sense and antisense strands worked equally at reducing transcript, – in an anti-sense experiment, a gene is constructed so that it produces a complementary strand to an expre ...
Mathew Sebastian Biology 303 Term Paper Schlank: a gene that
Mathew Sebastian Biology 303 Term Paper Schlank: a gene that

... collection of P-lines (Peter et al., 2002). These hemizygous schlank mutants did not grow as fast as the wildtype and also had pronounced growth defects which were dependent on the strength of the allele (Figure 1A–C). Schlank mutants that carried the stronger schlankG0349 gene, the case where schla ...
Do now - MrSimonPorter
Do now - MrSimonPorter

... In what ways are we different from each other (“variations”)? Can you now divide these differences between those that are inherited and those which are environmental and those which might be both. ...
Genetics Clicker - Solon City Schools
Genetics Clicker - Solon City Schools

... ear lobes. Farrah thought this was odd because her earlobes were attached and having attached earlobes is a dominant caused condition. What must be Farrah’s genotype and if Farrah has another child with a homozygous recessive man what are the chances that their baby will have free earlobes? 1. ee ...
Cystic fibrosis (CF) is an inherited disease that causes the body to
Cystic fibrosis (CF) is an inherited disease that causes the body to

... Americans, or 1 in every 20 people living in this country, is a CF carrier. And most of them don't know it. Parents can be tested to see if they carry the CF gene, but because there are hundreds of specific CF gene mutations (not all of which are known), genetic testing for CF won't detect everyone ...
The Principle of Segregation
The Principle of Segregation

... Probability- the chance that a particular event will occur A. Each trait segregates independently so offspring have a 50/50 chance of inheritance (50% father vs. 50% mother) B. Past outcomes do not affect future ones C. An individual outcome is the product of all the events. ( 1/2 x 1/2 x 1/2 = 1/8 ...
Gene Section ATF3 (activating transcription factor 3) Atlas of Genetics and Cytogenetics
Gene Section ATF3 (activating transcription factor 3) Atlas of Genetics and Cytogenetics

... ATF3 is a member of the CREB/ATF family of transcription factors and both homodimerize and heterodimerize with other members of CREB/ATF family, including C/EBPg, CHOP/DDIT3, ATF2, Jun, JunB, p21SNFT/JDP1, and Nrf2/NFE2L2. ATF3 and various heterodimers containing ATF3 has been shown to bind to a con ...
Supplemental Information - Molecular Cancer Research
Supplemental Information - Molecular Cancer Research

... Specifically, closed frequent itemsets (a condensed form of frequent itemset results) were extracted from the full list of insertion locations (mapped to their nearest gene) using an apriori-based algorithm (6-8). The result of this algorithm was a list of candidate gene sets that occur in at least ...
Leukaemia Section t(2;11)(q31;p15) NUP98/HOXD13 t(2;11)(q31;p15) NUP98/HOXD11 Atlas of Genetics and Cytogenetics
Leukaemia Section t(2;11)(q31;p15) NUP98/HOXD13 t(2;11)(q31;p15) NUP98/HOXD11 Atlas of Genetics and Cytogenetics

... NUP98 (nucleoporin 98kDa) Location 11p15 DNA/RNA NUP98 gene, located on chromosome 11p15, encodes a 98-KD protein a component of nuclear pore complex (NPC). NUP98 is found in the nucleoplasmic and cytoplasmic domains of the NPC, and functions as a transport co-factor of RNA and protein between the n ...
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4.16.08 105 lecture

... You inherited one copy of each of your genes from your mom and one from your dad. The genes from your mom and dad are similar but not identical. For example, you inherited two copies of the LDL receptor gene. They may be identical but there is a very good chance that some of the nucleotide letters a ...
From Genes to Behavior: Outline
From Genes to Behavior: Outline

... Some questions: what happens to montane vole (and mice) given prairie vole receptor gene? they became more affiliative with their mated partners Do we also need an environmental signal to release vasopressin? Sex → release of vasopressin → male gets “addicted” to his mate. So environment matters, bu ...
GENE THERAPY - Ashland Independent Schools
GENE THERAPY - Ashland Independent Schools

... Who decides which traits are normal and which constitute a disability or disorder? Will the high costs of gene therapy make it available only to the wealthy? Could the widespread use of gene therapy make society less accepting of people who are different? Should people be allowed to use gene therapy ...
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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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