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file - ORCA - Cardiff University
file - ORCA - Cardiff University

... TriNEx an additional DNA cassette termed SubSeq is used, which donates a new trinucleotide sequence back to the target gene. MlyI is used to achieve trinucleotide exchange by means of the mechanism outlined in Fig. 2. The donating sequence in SubSeq is determined by the user and can be randomized (1 ...
seq.
seq.

... Xenologs: gene was obtained by organism through horizontal transfer. The classic example for Xenologs are antibiotic resistance genes, but the history of many other molecules also fits into this category: inteins, selfsplicing introns, transposable elements, ion pumps, other transporters, Synologs: ...
Journal of Renin-Angiotensin-Aldosterone System
Journal of Renin-Angiotensin-Aldosterone System

... octapeptide angiotensin II (Ang II) through the action of angiotensin-converting enzyme (ACE), a membrane- bound, zinc metalloendopeptidase involved in the metabolism of many small peptides. ACE and angiotensinogen play an important role in blood pressure and blood volume homeostasis.3 Thus, it is n ...
list of publications
list of publications

... In multicellular organisms, the division of a single totipotent cell, the homologues are highly conserved, and a substantial number of papers describe fertilized zygote, ultimately results in a myriad of cells with different structures their mode of action, it remains unknown how any of these protei ...
Mechanistic Models of Cancer in the Space of Pathways
Mechanistic Models of Cancer in the Space of Pathways

... Dynamics of Cancer Progression ...
molecular genetics of coat colour in pigs
molecular genetics of coat colour in pigs

... pigmentation in a large number of vertebrates, including the pig (Kijas et al. 1998; 2001). The MC1R gene is probably the better characterized coat colour gene in Sus scrofa. It is constituted by a single coding exon of about 950 bp that has been sequenced in a large number of pig breeds with differ ...
Intrinsic and extrinsic contributions to stochasticity in gene expression
Intrinsic and extrinsic contributions to stochasticity in gene expression

... comes about in two ways. The inherent stochasticity of biochemical processes such as transcription and translation generates ‘‘intrinsic’’ noise. In addition, fluctuations in the amounts or states of other cellular components lead indirectly to variation in the expression of a particular gene and th ...
the contribution of gene movement to the two rules of speciation
the contribution of gene movement to the two rules of speciation

... introduce these mechanisms below, returning to the evidence for each in the next section. There are three mechanisms by which genes can move between chromosomes. The first involves the simple movement of a gene from one chromosome to another with no duplicative intermediate. Movement of large chromo ...
Estonian HumanGenesResearchAct.
Estonian HumanGenesResearchAct.

... of health shall maintain the confidentiality of the identity of the gene donor, his or her tissue sample, the description of his or her state of health and his or her genealogy and shall deliver the personal data of the gene donor, the tissue sample, the description of his or her state of health and ...
Role of Cryptic Genes in Microbial Evolution1
Role of Cryptic Genes in Microbial Evolution1

... to absence of the gene for a lactose permease (lacy gene). It does possess a 1acZ (@galactosidase) gene that is homologous with the 1acZ gene of E. coli, and a fully functional repressor (lacl) gene. In the absence of the permease gene, the P-galactosidase gene plays no functional role in lactose ut ...
Genome Research 13, 8 - Tel
Genome Research 13, 8 - Tel

... Department of Computer Science, Tel-Hai Academic College, Upper Galilee 12210, Israel A new measure for gene prediction in eukaryotes is presented. The measure is based on the Discrete Fourier Transform (DFT) phase at a frequency of 1/3, computed for the four binary sequences for A, T, C, and G. Ana ...
The Jumping SHOX Gene—Crossover in the Pseudoautosomal
The Jumping SHOX Gene—Crossover in the Pseudoautosomal

... PAR1 is located at the terminal end of Xp and Yp. All genes within PAR1 escape X inactivation in women. However, the only gene in this region associated with human disease is the SHOX gene (10). Inheritance of LWD is pseudoautosomal. The SHOX gene in the normal situation is present in two functional ...
Polymorphisms of the PSD3 gene are associated with obesity in two
Polymorphisms of the PSD3 gene are associated with obesity in two

... There is a need to explore the genetic and epigenetic mechanisms involved in obesity initiation and development. ...
Localization of Three Genes in the Hook
Localization of Three Genes in the Hook

... karyotype. This allowed us to compare the spatial distribution of two DNA sequences on different chromosomes, and of two genes located on the same chromosome. Localization of the Three Genes in HamsterSperm Nuclei We next mapped the positions of each of the three genes within hamster sperm nuclei us ...
For the last three and a half billion years, evolution has been
For the last three and a half billion years, evolution has been

... documentation represents the shared rules that allow the three databases to exchange data on a daily basis. The range of features to be represented is diverse, including regions which: perform a biological function, affect or are the result of the expression of a biological function, ...
Ascidian embryogenesis and the origins of the chordate body plan
Ascidian embryogenesis and the origins of the chordate body plan

... transgcnic DNA and RNA into de\ eloping embryos. hlosaic incorporation is not ~1prohlcm in this system because of the small number of clca\~ges involved in the formation of adwnccd-stage embryos. ‘liansgenesis has been wed to characterize &rcgulatory I)NA elements that mediate tissue-specific and li ...
It`s All In The Genes - American Maine
It`s All In The Genes - American Maine

... chromosomes. Chromosomes are threadlike structures found in the nucleus of cells. Chromosomes carry genetic information. Humans have 23 pairs of chromosomes and cattle have 30 pairs. Chromosomes are always in pairs — one of each pair is inherited When I say “genes” from the mother (dam) and the othe ...
Microbial diversity and virulence probing of five different body sites
Microbial diversity and virulence probing of five different body sites

... mouse over redX to identify the metagenome identity Created figure in powerpoint to show clustering of COGs across metagenomes ...
osb week10 lab
osb week10 lab

... White spotted, or piebald, cats are very common. Spotting may occur with any coat color, and is mainly due to the effect of one gene with two co-dominant alleles. The spotted allele, S, is phenotypically expressed as white spots, while the s allele is expressed as no white spots or even any white ha ...
Text S1.
Text S1.

... rearing, one of which also curled in a ball when lifted up and 5 (15%) seemed tottery and fell from side to side when walking and curled up in a ball when lifted up. Since +/dfw lose their Preyer reflex by about 1-2 months of age, this test was not a useful discriminator for these mice. Compound het ...
Copy Number and Gene Expression Integration in Partek
Copy Number and Gene Expression Integration in Partek

... response, or remission is not available; therefore, sig-regions is more appropriate. However, chi-square is more useful if additional phenotypic information is available and will be used as grouping variables. For this example, use the Sig-Regions table, which includes segments that are observed in ...
Course Cat Desscription
Course Cat Desscription

... to continue in biological science. Man’s structure and function will be stressed as well as his relationship to other living things and to his environment. BSC 1010C 4 (3 / 2) GENERAL BIOLOGY I with Lab • Prerequisite: None • Satisfies Codes: BIOS, GENE, LABR • Laboratory Fee: $15 • Students must co ...
Slide 1 - Faculty Web Pages
Slide 1 - Faculty Web Pages

... het parent (write out all three possible gene orders if you have to). 7.) Re-write karyotypes for the parents and progeny based on the correct gene order 8.) Identify location of recombination event in the SCO progeny (between genes 1 and 2, or genes 2 and 3?) 9.) Determine map distances between gen ...
Heterogeneous lengths of copy number mutations
Heterogeneous lengths of copy number mutations

... nucleotide variations and copy number (CN) variations. CN variations represent genomic segments with a size range of ~100 bp to several Mbs demonstrating an altered (or non-neutral) dosage status.5 They are typically introduced in the genome by recombination-based or replication-based mechanisms. Th ...
The Schistosoma gene discovery program: state of the art
The Schistosoma gene discovery program: state of the art

... libraries of di€erent stages of the life cycle of S. mansoni and S. japonicum have been published by Network members [19,30±34]. In all of these studies, the authors report that the great majority of the selected cDNA clones (between 30 to >60%) consists of transcripts that could not be identi®ed by ...
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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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