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Gene Section RBM15 (RNA binding motif protein 15) in Oncology and Haematology
Gene Section RBM15 (RNA binding motif protein 15) in Oncology and Haematology

... Cytogenetics 60% of cases have the t(1;22) as a single anomaly; the remaining cases exhibit complex and hyperploid clones. Hybrid/Mutated gene 5' OTT - 3' MAL, comprisng most of OTT fused to most of MAL; the reciprocal 5' MAL - 3' OTT may or may not be present. Abnormal protein Includes most of OTT ...
Genetics
Genetics

... • A trait that is covered over, or dominated, by another form of that trait and seems to disappear • Hidden when the other copy of the gene contains the dominant allele. • A recessive allele shows up only when there is no dominant allele present • Shown with a lower-case letter ...
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... To evaluate the effects of transcription factor mutants, a combined metabolic and regulatory model was used to evaluate whether the deletion of a transcription factor is lethal for growth on glycerol minimal medium. ...
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... The success of the GO Consortium’s work has been to demonstrate the great utility of shared community ontologies in the genomics community. This success has inspired the development of similar ontologies for other domains and has promoted open collaborations among groups working on similar projects ...
Transcription Control in Eukaryotes
Transcription Control in Eukaryotes

... Eukaryotes Transcription control in eukaryotes is more complex than in prokaryotes, with more gene-gene interactions, presumably required to produce more different cell types in more complex organisms. We will consider some examples and models to illustrate some general principles. ...
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Gene set tes-ng

... ROAST gene set test •  The ques'on asked is “Do the genes in this gene set tend to be differen'ally expressed?” •  It is NOT compared rela've to other genes •  It is designed such that if > 25-50% of genes in the gene set are differen'ally expressed it will be significant •  It uses sophis'cate ...
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Gene Section RNASET2 (ribonuclease T2) Atlas of Genetics and Cytogenetics

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Quick Unit Summary A gene is a stretch of DNA that codes for a
Quick Unit Summary A gene is a stretch of DNA that codes for a

... A gene is a stretch of DNA that codes for a specific characteristic or physical trait. Organisms always have 2 copies of each gene- the one they inherited from their biological mother and the one they inherited from their biological father. Genes have varying levels of expression, referred to as dom ...
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BB30055: Genes and genomes

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cDNA cloning, expression and chromosomal localization of the

... ATCCCC-3´) and amplified by PCR a fragment from human genomic DNA (Clontech). We cloned the fragment in pGEM-Teasy vector and sequenced it in both directions confirming the sequence of the EMBL entry AC005874. The analysis of the sequence cloned, strongly suggested that this genomic fragment might c ...
Gene Section AML1 (acute myeloid leukemia 1) Atlas of Genetics and Cytogenetics
Gene Section AML1 (acute myeloid leukemia 1) Atlas of Genetics and Cytogenetics

... Mariano Rocchi, Resources for Molecular Cytogenetics. Laboratories willing to validate the probes are welcome: contact M Rocchi. ...
Uses of Genomic Information in the Diagnosis of Disease
Uses of Genomic Information in the Diagnosis of Disease

...  http://www.cdc.gov/nchs/fastats/deaths.htm ...
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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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