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Albinism Powerpoint
Albinism Powerpoint

... All Green= homozygous dominant, person have disorder and 2 copies of the “bad” gene Half Green/Half White= because this is a dominant disorder (rules of dominance), the person has the disease and only has one copy of the “bad” gene and one copy of the “healthy” gene. ...
9 Genetics Vocabulary
9 Genetics Vocabulary

... 15. law of segregation—Only one version (allele) of a gene is passed on to each sex cell 16. law of independent assortment—Different genes are passed on independently of one another 17. monohybrid cross—predicts the inheritanxce of ONE trait (4 boxes) 18. dihybrid cross—predicts the inheritance of T ...
Functional genomics strategy from gene discovery to evaluation of
Functional genomics strategy from gene discovery to evaluation of

... During the screening, we identified a maize clone (SAT2) that seemed to confer elevated salt tolerance in comparison to control cells. SAT2 cDNA encodes a 70-kDa protein which is 67 % identical to the Arabidopsis GA MYB-binding protein (AtSAT2). To further examine salinity tolerance in Arabidopsis, ...
Genomics of sensory systems - University of Maryland
Genomics of sensory systems - University of Maryland

... 3. Failure of meiosis ...
Pre – AP Biology
Pre – AP Biology

... (Brown, blue, green eye color. These are three different versions or DNA sequences of a single gene, but they all are making the eye color.) Each trait needs two alleles. One from each parent to be made or “expressed”. Dominant alleles are given capital letters. (These are like books or recipe cards ...
Genetic Disorder Template
Genetic Disorder Template

... Make a punnett square to demonstrate the probability per child depending on the parents Make more than one punnett square. Parents determine the ratio of probability of offspring having the genetic disorder. Explain(see below) to the class how the punnett square works. Female is on the left and f ...
Supplementary Materials and methods (doc 46K)
Supplementary Materials and methods (doc 46K)

... sites ‘CATG’ were identified and +/- 17 bases of flanking sequence were extracted in silico using the Ensembl Perl application programming interface from all genes annotated in Ensembl version 58 and stored in a MySQL database. The sequences were extracted from all annotated spliced and unspliced tr ...
Tuberous sclerosis (TS) - Nottingham University Hospitals NHS Trust
Tuberous sclerosis (TS) - Nottingham University Hospitals NHS Trust

... Tuberous sclerosis (TS), also known as tuberous sclerosis complex (TSC), is a genetic condition that affects many different systems in the body. Its effects vary greatly between individuals, even within the same family, with some people being so mildly affected they don't know they have it, while ot ...
A Separate Peace – Pre
A Separate Peace – Pre

...  Finny’s personal rules.  The effect of the war on the seniors.  Gene’s description of Finny’s physical ability.  Gene’s view of America and the war.  Finny’s openness/honesty. Discussion Questions:  Gene describes Finny’s mind as being the “opposite” of his. What does he mean by this?  What ...
Document
Document

... Are genes added or lost from metabolic networks one at a time, or does network evolution proceed by steps involving whole sets of genes simultaneously? Modules of physiologically coupled genes might be the best candidates for simultaneous acquisition or loss during evolution. Identified physiologic ...
Forces of Microevolution Examples
Forces of Microevolution Examples

... found that laboratory mice carrying [heterozygous for] cystic fibrosis genes did not suffer the deadly diarrhea that is typically caused by cholera. This, said a researcher who conducted the study, Dr. Sherif E. Gabriel, may explain why cystic fibrosis is one of the most common gene defects. ‘The fr ...
Gene mutation
Gene mutation

... - What is meant by ‘mutation’? - When/how do they happen? - What sort of impact might they have? ...
Final
Final

... Could a synthetic Mycoplasma genome be “sparked” to life using an E. coli donor cytoplasm? Why or why not? According to Venter, how might this have been an advantage in his research? ...
Human Endogenous Control Gene Panel
Human Endogenous Control Gene Panel

... With good quality cDNA and good pipetting technique, very high reproducibility is possible. Low amounts of cDNA can lead to higher variation. Also, low quality cDNA can lead to big differences between replicates. Check the accuracy and reproducibility of your pipettes. • The signal for 18S rRNA come ...
Genetic Technology
Genetic Technology

... Dog breeders wanted to breed a dog that would run fast but also be born with long, shiny fur, looking for the best characteristics from the parents. ...
What is DNA? - Livingstone High School
What is DNA? - Livingstone High School

... Why is DNA Interesting? • DNA is a nonliving molecule. • There are 6 feet of it in every cell. • The human body can have as many as ten thousand trillion cells, and almost every one of them has 6 feet of densely compacted DNA. • DNA is unique for every individual • DNA controls all the activities i ...
Statistical analysis of DNA microarray data
Statistical analysis of DNA microarray data

... – Ratio of connectivity: for a subgraph with K nodes and L edges r = L/(K(K-1)/2). – K-core: a subgraph in which every node is connected to at least K other nodes (within this subgraph). ...
Result certificate #012345 Detection of mutation insertion of
Result certificate #012345 Detection of mutation insertion of

... Explanation Presence or absence of insertion of retrotransposon in GRM1 gene causing neonatal ataxia (BNAt - Bandera's neonatal ataxia) in Coton de Tulear was tested. BNAt is a neurological symptom consisting of a lack of normal coordination of movements beginning in puppies after birth. Mutation th ...
BEBERAPA MUTASI GEN katG
BEBERAPA MUTASI GEN katG

... with PyMOL program showed 316 amino acid residues near the active site binding INH. Catalase-peroxidase simulation with PyMOL program showed 290 amino acid residues located in the N terminus loop area and relatively far from the active site, the effect of these mutations and their relationship in th ...
outline21590
outline21590

... c. HGP began 1990 d. Joint effort by DOE and NIH e. Estimated completion 15 years f. Working draft announced June 2000 2. HGP - Working Draft a. 16 Sequencing centers b. 22.1 billion bases of raw data c. 30% high quality finished sequence d. Map of 90% of genes on every chromosome e. 3164.7 million ...
Bringing an Ag Biotech Seed Product to Market
Bringing an Ag Biotech Seed Product to Market

... X May not be expressed in planta X No efficacy X Scientifically feasible, market cannot support ...
GO: The Gene Ontology
GO: The Gene Ontology

... Finding GO terms In this study, we report the isolation and molecular characterization of the B. napus PERK1 cDNA, that is predicted to encode a novel receptor-like kinase. We have shown that like other plant RLKs, the kinase domain of PERK1 has serine/threonine kinase activity, In addition, the lo ...
BIOL 1406-61313 CHAPTER 14 AND 15 Dr
BIOL 1406-61313 CHAPTER 14 AND 15 Dr

... 3. In general, the frequency that crossing over occurs between two linked genes depends on _____. how far apart they are on the chromosome the phase of meiosis in which the crossing over occurs whether the genes are on the X or some other chromosome whether the genes are dominant or recessive the ch ...
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 ...
Document
Document

... mammals, occurring early in embryonic life, at about the time of implantation. ...
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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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