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Interplay between the transcription factors acting on
Interplay between the transcription factors acting on

... fragment containing the promoter, the coding region, and the 39 noncoding region (positions 2800–1930) of the UGA3 gene into the ...
The wbbD gene of E. coli strain VW187
The wbbD gene of E. coli strain VW187

... subunits is thought to occur at the cytosolic face of the plasma membrane (Whitfield and Valvano, 1993). Four additional sugars are subsequently added to the GlcNAc-PP-Und intermediate to complete the formation of the O7 subunits. These reactions are catalyzed by specific glycosyltransferases, which ...
Albinism - Harlem Children Society
Albinism - Harlem Children Society

... substances applied topically to the skin and mucous membranes. J. Pharmacol. and Exp. Therapeutics. 82, ...
Marfan syndrome in the third Millennium
Marfan syndrome in the third Millennium

... Nosology: What is Marfan syndrome today ? Marfan syndrome (MFS, OMIM#154700) is an autosomal dominant connective tissue disorder that has an estimated incidence of 1/5000 with probably over 25 % of sporadic cases. The syndrome involves many systems (skeletal, ocular, cardiovascular, pulmonary, skin ...
NIHMS88703-supplement-2
NIHMS88703-supplement-2

... Overlap between liver signature genes from mouse models and a macrophage-enriched metabolic network (MEMN) Based on the co-expression networks constructed from liver and adipose tissues collected from a mouse cross between C57BL/6J (B6) and C3H/HeJ on an apolipoprotein E null background (BXH/apoE), ...
10849-ME2-Nutrilite (20-61)
10849-ME2-Nutrilite (20-61)

... suspended particles that don’t dissolve. It’s just the nature of the material. It’s like the pulp in orange juice. How old must a baby be before it can take NUTRILITE Protein? A baby should be at least one year old before consuming NUTRILITE Protein. In very young children, it is best to limit NUTRI ...
A Customized Gene Expression Microarray
A Customized Gene Expression Microarray

... the Brittle Stalk2 (bk2) gene of maize and the Brittle Culm1 (bc1) gene of rice encode glycosyl phosphatidylinositol-anchored Cobra-like proteins (Li et al., 2003; Ching et al., 2006; Brady et al., 2007; Sindhu et al., 2007). Although the precise biological function of Cobra-like proteins has not be ...
Microsatellite Polymorphism in the Heme Oxygenase
Microsatellite Polymorphism in the Heme Oxygenase

... nucleotide polymorphisms (SNPs) are present in linkage disequilibrium with this microsatellite allele. Transcription of the HO-1 gene is under the regulation of the fine tuning system that includes the Bach-1 repressor (28) and (GT)n spacer polymorphism. To confirm our findings, further studies are ...
apgenetics1206 - cloudfront.net
apgenetics1206 - cloudfront.net

... 9) The allele for pea comb (P) in chickens is dominant to that for single comb (p), but the alleles black (B) and white (B’) for feather color show partial dominance, B/B’ individuals having “blue” feathers. If birds heterozygous for both alleles are mated, what proportion of the offspring is expec ...
Genetic Approaches to Studying Genome Function
Genetic Approaches to Studying Genome Function

... SUPPRESSION: A given mutation (A) has a discrete phenotype that is not normal, i.e. not wild-type. The presence of the second mutation (B, the suppressor mutation) causes the AB double mutant to display a phenotype that is normal or near-normal. Thus, a suppressor mutation rescues or restores or re ...
Characterisation of the Aspergillus niger dapB gene, which encodes
Characterisation of the Aspergillus niger dapB gene, which encodes

... transformants were assayed for DPP IV activity (Fig. 3b). A five to sevenfold increase in DPP IV activity was measured in the cell-free extracts of the DapB transformants compared to the control strain. This increase is clearly significant and shows that increased dapB mRNA levels correlate with highe ...
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... (iii) Suggest why this behaviour may help flatworms survive in the streams where they live. ...
Gene Expression in Thyroxin-Induced Metamorphosing Axolotl Hearts
Gene Expression in Thyroxin-Induced Metamorphosing Axolotl Hearts

... The Mexican axolotl (Ambystoma mexicanum) is a unique model to study vertebrate heart development for several reasons. In addition to the wild-type animal, there is also an embryonic lethal condition caused by a homozygous recessive mutation in cardiac gene “c” [1,2]. These mutant embryonic hearts d ...
Ensembl Compara Perl API
Ensembl Compara Perl API

... blast hits’ Paralogues for a selected set of species No global view of the evolution history of the gene considered ...
Age study
Age study

... Figure 11: Configuring the Properties dialog box to display the random effect check-box The rest of this tutorial will discuss how different ANOVA models can affect the statistical and biological results of the data explored thus far, specifically by comparing a one-way ANOVA model and a multi-fact ...
Imunocytochemistry Detection of M1CA Gene Receptor in Human P
Imunocytochemistry Detection of M1CA Gene Receptor in Human P

... macrophages, which are the major effectors facilitating killing and inhibiting replication of Brucella. The Th1 cell induced - cytokines, like IFN- γ, are important for the ctivation of macrophages and in resistance to in vivo and in vitro Brucella infections (Zhan et al., 1993)) . gamma interferon ...
Human Traits Lab
Human Traits Lab

... 55 An offspring inherited a dominant allele from one parent and a recessive allele from the other parent for the same trait. Which of the following is a possible explanation for what will be exhibited by the offspring for that trait? A The offspring will exhibit the recessive trait with the dominant ...
Modulation of CTCF Insulator Function by
Modulation of CTCF Insulator Function by

... that ncRNA transcription is necessary for the changes in chromatin features within the 3 kb region and for the subsequent eviction of CTCF from its occupancy site. In summary, evidence presented by Lefevre et al. (2008) supports a model in which transcription-dependent chromatin remodeling leads to ...
1 - StangBio
1 - StangBio

... d. With respect to the gene for flipper length in bottlenose dolphins, if the allele T produces stunted non-functional flippers and the allele t produces normal flippers, then a dolphin with the genotype tt will have this phenotype: ________________. e. Huntington’s Disease in humans is caused by th ...
What stay-green mutants tell us about nitrogen remobilization in leaf
What stay-green mutants tell us about nitrogen remobilization in leaf

... polymorphisms in corresponding cDNAs. An example is UDP-glucose pyrophosphorylase (UDPGP). The stay-green gene from F. pratensis was transferred to L. temulentum Ceres and the alien segment reduced by several backcrosses (Thomas et al., 1999). Figure 5a shows that the small introgressed segment carr ...
miRNA pptx - NUS School of Computing
miRNA pptx - NUS School of Computing

... Some intergenic miRNAs are clustered with each other; according to (Saini et al. 2007) most of these clusters use the same pri-mirNA transcript Use method 1 for neighboring miRNA to get the intergenic miRNA expression approximation ...
Primary and secondary metabolism, and post
Primary and secondary metabolism, and post

Biology 40S Genetics Booklet (StudentsCopy2)
Biology 40S Genetics Booklet (StudentsCopy2)

Ketoglutarate Dehydrogenase Complex
Ketoglutarate Dehydrogenase Complex

... of the human proteins are known. The organization of the proteins into a large, ordered multienzyme complex (a “metabolon”) has been well studied in prokaryotic and eukaryotic species. KGDHC catalyzes a critical step in the Krebs tricarboxylic acid cycle, which is also a step in the metabolism of th ...
Transgenic approaches to microbial disease resistance in crop
Transgenic approaches to microbial disease resistance in crop

... about their specificity and specific activity. By using a fungally derived chitinase, one might assume to be working with an enzyme optimized for degrading fungal cell walls. Consistent with this notion, a Rhizopus chitinase expressed in tobacco conferred resistance to a Sclerotinia pathogen. No res ...
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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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