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A novel frameshift mutation of HEXA gene in the
A novel frameshift mutation of HEXA gene in the

... is a lysosomal enzyme composed of one α- and one β-subunit which are encoded by the HEXA and HEXB genes, respectively. TSD is caused by mutations in the HEXA gene (MIM*606869) located on chromosome 15q23-q24.1,2 The HEXA gene consists of 14 exons and contains 1,587 bp of coding sequence encoding a 5 ...
Continuous Representations of Time Series Gene Expression Data
Continuous Representations of Time Series Gene Expression Data

... Recently, several papers have focused on modeling and analyzing the temporal aspects of gene expression data. In Holter   [10] a time translational matrix is used to model the temporal relationships between different modes of the Singular Value Decomposition (SVD). Unlike our work, this method ...
Genetic Characteristic of the Usual Form of the Polydactyl Gene in
Genetic Characteristic of the Usual Form of the Polydactyl Gene in

... The standard footed kitten can be show. Due to their heavy boning because of their poly heritage, they can do well on the show bench. Other Dominant Genes, Manx A dominant gene that causes serious health issues, is the Manx gene or the tail shortening gene. As reported by Robinson, 2nd edition, (197 ...
Leukaemia Section t(11;14)(q24;q32) IGH/miR -125b-1 Atlas of Genetics and Cytogenetics
Leukaemia Section t(11;14)(q24;q32) IGH/miR -125b-1 Atlas of Genetics and Cytogenetics

... leukemic recurrence as bilateral ovarian tumors 7 years after allogenic bone marrow transplantation for BCPALL. Chapiro et al. reported two further adult cases: a female patient aged 45 years with an early-pre-B phenotype who died 21 months after diagnostic, and a male patient aged 33 years who were ...
Document
Document

... Makes systematic RNAi screens possible ~ 75% of time, RNAi gives a reduction in RNA levels (Not 100% silencing but leaky) Has been used to reduce expression of genes  On particular chromosomes, or  Expressed at a particular developmental time © 2005 Prentice Hall Inc. / A Pearson Education Company ...
Exploring the genomic traits of fungus
Exploring the genomic traits of fungus

... of genomic diversity between these strains. Each of the six genomes includes 125 to 835 orthologous groups that are unique (Fig. 2a). Species core orthologous clusters and strain-specific unique clusters within the three Collimonas species were examined, respectively (Fig. 2b-d). In the three specie ...
The complete nucleotide sequence of the chick a
The complete nucleotide sequence of the chick a

... are similar but not identical. In a l l , 6 different actin iso-proteins have been identified in birds and mammals (3,1*,?). Four of these are a-actins or muscle actins obtained from 1* different muscle tissue types (skeletal striated, cardiac striated, vascular smooth, and enteric smooth). The a-ty ...
Multiple Testing Corrections
Multiple Testing Corrections

... correct for occurrence of false positives. In microarray data analysis, false positives are genes that are found to be statistically different between conditions, but are not in reality. B. Importance of Multiple testing corrections A typical microarray experiment measures several thousand genes sim ...
Gene Section ASNS (asparagine synthetase) Atlas of Genetics and Cytogenetics
Gene Section ASNS (asparagine synthetase) Atlas of Genetics and Cytogenetics

... Identity Other names: TS11 HGNC (Hugo): ASNS Location: 7q21.3 ...
Document
Document

... All downloads and use of the Osprey Network Visualization System are subject to the following terms: As long as you comply with the terms of this Agreement, you are granted a non-exclusive license to install and use the Software on a single computer for educational, research, and not-forprofit purpo ...
Phylogenetic, amino acid content and indel analyses
Phylogenetic, amino acid content and indel analyses

... rpoB genes of Mycobacterium tuberculosis (EMBL accession no. U12205), Mycobacterium leprae (Z14314), Mycobacterium smegmatis (U24494), Bacillus subtilis (L24376) and Staphylococcus aureus (X64172) and the rplL genes of Escherichia coli (V00339) and Staphylococcus aureus (X64172). PCRs were performed ...
New Gene for Bacterial Blight Resistance in Rice Located
New Gene for Bacterial Blight Resistance in Rice Located

... Pi-ta encodes the NBS-LRR type protein (1). The present study also located two closely linked NBS sequences to the centromeric region of chromosome 12. R proteins containing NBS motif also have the LRR motif according to the structures of cloned R genes; this suggests that there is at least one NBS- ...
GO2PUB - GenOuest
GO2PUB - GenOuest

... Literature search on PubMed takes more and more time as PubMed growths. There is a need for automated search tools, which must have a better precision and recall than PubMed basic query system. We developped GO2PUB to answer this demand in the field of the genetics. Our purpose was to use the knowle ...
Estimating lethal allele frequencies in complex pedigrees via gene
Estimating lethal allele frequencies in complex pedigrees via gene

... from animals born in 2000 and 2005 were drawn. Gene counting method (GC) The GC method was proposed by ALLAIRE et al. (1982). This approach calculates the expected lethal allele frequency from known individual genotypes (carriers) among a set of relevant ancestors. Here we used a Fortran program wri ...
gene_expression
gene_expression

... GO-based annotation assigns GO terms to a gene ...
Galactosemia screening when?
Galactosemia screening when?

... galactosemia known as type III or galactose epimerase deficiency. ...
II. Purpose of Meiosis #1
II. Purpose of Meiosis #1

... This outline is the same as is found in your Lecture Guide. In order to obtain an overview of the material in the Lecture Guide and to be able to see the ‘big’ picture while you study, fill in the missing components of the following outline from the Lecture Guide. ...
Resveraterol-Curcumin Extreme-P53
Resveraterol-Curcumin Extreme-P53

... When p53 itself is flawed, however, it allows other cancer-causing genes (known as oncogenes) to hijack the cell's control machinery and set it free to spread wildly _ the hallmark of cancer. "Loss of p53 function in cells leads to uncontrolled proliferation and promotes cancer development," Olivier ...
Severe Perinatal Thrombosis in Double and Triple Heterozygous
Severe Perinatal Thrombosis in Double and Triple Heterozygous

... Met570 Thr substitution being the pathological lesion in the family was provided by sequence analysis of exon XIV from 50 controls (of Caucasian origin with no history of venous thrombosis), which failed to detect another example of the Met570 Thr substitution. This mutation does not appear to be a ...
The evolution of large DNA viruses: combining genomic information
The evolution of large DNA viruses: combining genomic information

... increased and ribozyme activity evolved, the micelles became protoviruses, developed proteins and frequently fused, sharing information. Eventually, some evolved into protocells. It has also been proposed that viruses were the first to use DNA to protect their genetic material from degradation by th ...
PDF
PDF

... Background: SRY-positive XX testicular disorder of sex development (DSD) caused by X;Y translocations was not yet reported in domestic animals. In humans it is rarely diagnosed and a majority of clinical features resemble those which are typical for Klinefelter syndrome (KS). Here we describe the fi ...
Conditions for gene disruption by homologous
Conditions for gene disruption by homologous

... (Zolghadr et al. 2007). To test different post-electroporational conditions, PBL2025 cells were prepared as described in the Materials and methods and electroporated with 300 ng of pSVA78 plasmid DNA (Table 2). This plasmid harbors the lacS gene with flanking regions of the Sso02684 and Sso2681 gene ...
Slide 1
Slide 1

... What is Genetic Engineering? …the branch of biology that uses special procedures and techniques to change an organism’s DNA. One example is removing DNA from one organism and inserting it into another organism. In this image, the gene for insulin has been remove from human DNA and inserted into a ba ...
A Phylogenomic Approach to Bacterial Phylogeny
A Phylogenomic Approach to Bacterial Phylogeny

... species (see Methods) revealed that a group of genes possess with low support for several deep branches was obtained. This similar topologies for the bacterial part of the tree. This group topology is however in general agreement with the rRNAcontains almost all informational genes contained in the ...
Migration and mutation
Migration and mutation

... [4] Class [3] refers to migration of individual genes rather than pairs of genes, as expected if migration involves diploid individuals. Our first paper [5], which I wrote, with migration from the mainland into a single island population, ignores this complication. I have to admit that I entirely fo ...
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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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