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Small, K, Wagener, M and Warren, ST: Isolation and characterization of the complete mouse emerin gene. Mammalian Genome 8:337-341 (1997).
Small, K, Wagener, M and Warren, ST: Isolation and characterization of the complete mouse emerin gene. Mammalian Genome 8:337-341 (1997).

... protein to the nucleoplasm (Furakawa et al. 1995). Emerin is a primarily hydrophilic protein with a hydrophobic, C-terminal domain, similar to that of LAP2. Moreover, immunofluorescence microscopy showed that emerin also localizes to the nuclear membrane (Manilal et al. 1996; Nagano et al. 1996). Ta ...
Post-transcriptional modifications Cap a
Post-transcriptional modifications Cap a

... In some cases, mobile, sequence-specific silencing signals can move from cell-to-cell or even over long distances in the plant. Several current models hold that silencing signals are “aberrant” RNAs (aRNA), that differ in some way from normal mRNAs. The most likely candidates are small antisense RNA ...
Alterations of the PPP2R1B gene located at 11q23 in human
Alterations of the PPP2R1B gene located at 11q23 in human

Detection of complex mutations in Swedish FAP familes
Detection of complex mutations in Swedish FAP familes

... partially related to the mutation site or type. In our material, 96 unrelated FAP patients from the Swedish polyposis register were screened for mutations in the APC gene. By using a combination of several different mutation detection techniques, the mutations were revealed in >95% in families with ...
09_01.jpg
09_01.jpg

... (ContigView, MultiContigView, SyntenyView, GeneView) ...
Genetics Practice II
Genetics Practice II

... Baldness in humans is a dominant, sex-influenced trait. This gene is on the autosomes, not the sex chromosomes. A man who is BB or Bb will be bald and will be normal only if he is bb. A woman will only be bald if she is BB and normal if she is Bb or bb (it’s almost like B is dominant in males and b ...
Chapter 7 (Genetics of Organisms)
Chapter 7 (Genetics of Organisms)

... Gregor Mendel's work was done about 140 yrs. ago, but even now much of what we know about genetics is based on Mendel's work and illustrated by it. Gregor Mendel was born in 1822 on a farm in Heinzendorf, Austria. At age 21 entered the Augustinian order of the Roman Catholic Church. As a monk he - s ...
Chapter 7/8-Animal Biotechnology
Chapter 7/8-Animal Biotechnology

... And for reporter constructs, see http://bcs.whfreeman.com/lodish5e/pages/bcsmain.asp?v=category&s=00010&n=15000&i=15010.01&o=|00510|00610|00520|00530|00540|00560|00570|00590|00600|00 ...
Problem Sets Fall 1995
Problem Sets Fall 1995

... In this model there are two pathways which can produce blue pigment. In a wild-type flower blue stripes are produced via the action of the A gene product. The A gene is only expressed in every other stripe. In the white stripes of a wild-type flower the B gene product inhibits the function of a thir ...
Cognitvie Psychology
Cognitvie Psychology

... 2. Dishabituation 3. Generalization ...
the genetics of tyrosinemia type i
the genetics of tyrosinemia type i

... makes enough that they will not have tyrosinemia. The other copy of the gene makes up for the one with the mutation. These people are carriers because they carry one mutated copy of the gene, which can be passed on to their children. This means, that as a parent of a child with tyrosinemia, both you ...
GM bacteria
GM bacteria

... Examples of GM Bacteria Being Used Genetically Altered Bacteria Could Block Malaria Transmission Scientists have discovered a way to help stop the spread of malaria by genetically altering a bacterium that infects about 80 percent of the world’s insects. Malaria is primarily transmitted through mos ...
Lecture 4 - University of California, Santa Cruz
Lecture 4 - University of California, Santa Cruz

... Lethal mutations arise in many different genes. These mutations remain “silent” except in rare cases of homozygosity. A mutation produces an allele that prevents production of a crucial molecule Homozygous individuals would not make any of this molecule and would not survive. Heterozygotes with one ...
Genetic Evolution Note Review
Genetic Evolution Note Review

... 22. What is the genotype of the dark animals, and what is it’s phenotype? 23. What happened to the number of recessive alleles in the population over the 30 generations? 24. For the change in the frequency of alleles to occur, there was a change in the environment to favor the darker trait. Give an ...
Current Comments@ I EUGENE GARFIELD
Current Comments@ I EUGENE GARFIELD

... by Miescher, 1897.”The referenceis to a mmpilation of Miescher”s work for the previous 30 years. Muller remarks that “only recently has it become reasonably cetmm+hmugh the analogous finding in Vimse+4 at it is redly this major cmnponentrather than sorm elusive accompaniment of it which constitutes ...
CHAPTER 10
CHAPTER 10

... Answer: Benzer first determined the individual nature of each gene by showing that mutations within the same gene did not complement each other. He then could map the distance between two mutations within the same gene. The map distances defined each gene as a linear, divisible unit. In this regard, ...
Chapter 5 I. Multiple Alleles
Chapter 5 I. Multiple Alleles

... Summary points 1. Dominance is a function of interaction between alleles. 2. Epistatsis is a function of interaction between genes. ...
EXTENSION OF MENDELIAN INHERITANCE: BEYOND
EXTENSION OF MENDELIAN INHERITANCE: BEYOND

... in the reaction to produce the step 1 product, and gene P controls the second step in the reaction to produce anthocyanin. These genes control flower color by controlling pea plant biochemistry, in particular that related to pigment compounds called anthocyanins. In peas, there is a two-step chemica ...
Self-Quiz Questions Activity 1: When is a Genome
Self-Quiz Questions Activity 1: When is a Genome

... Individuals within a species are so unique that having a single sequence is insufficient to characterize a species’ genome. Without knowing the number, the function, and the location of genes within a genome, the sequence is not very useful. Many sections of a genome are too difficult to sequence an ...
When Is a Genome Project Finished?
When Is a Genome Project Finished?

... Individuals within a species are so unique that having a single sequence is insufficient to characterize a species’ genome. Without knowing the number, the function, and the location of genes within a genome, the sequence is not very useful. Many sections of a genome are too difficult to sequence an ...
Kinases
Kinases

... There is evidence of multiple changes at some loci (fig 4); eg TrC, shows 240 mutations in the course of its evolution from S1, but differs in only 124 amino acids from it. However, if the constancy of certain sequences of amino acids indicates their functional consistency 5,6, then the least certai ...
Cystic Fibrosis - Rady Children`s Hospital
Cystic Fibrosis - Rady Children`s Hospital

... the Children’s Hospital and Health Center/University of California, San Diego Cystic Fibrosis Center can be reached at 858-966-6790. Call the Adult CF Program at 858-657-8628 for questions about adults with CF. The Children’s Hospital and Health Center/University of California, San Diego Cystic Fibr ...
Supplemental Text. Informational genes undergo inter
Supplemental Text. Informational genes undergo inter

... Holliday junctions resolution. Holliday junctions are DNA structures that are formed during homologous recombination – a fundamental cellular process mostly used to rearrange genes and accurately repair DNA double-strand breaks. These four-way DNA junctions need to be resolved to allow proper chromo ...
Microarray Lessons Packet - McCarter Biology
Microarray Lessons Packet - McCarter Biology

... personalized medicine. The raw material of evolution is random mutation at the DNA level. These mutations (variation) may result in an improvement of “fitness” to the environment, may be of no consequence, or may be detrimental to an organism. In some cases, variations in DNA can have serious ramifi ...
Gregor Mendel, 1822-1884
Gregor Mendel, 1822-1884

... and her new baby is Type B. Consider these three putative fathers: can any be the biological father? Why or why not? #1 (Type A): Yes or No? #2 (Type B): Yes or No? #3 (Type O): Yes or No? ...
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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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