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Deletion Map of Chromosome 9 and p16 (CDKN2A) Gene Alterations
Deletion Map of Chromosome 9 and p16 (CDKN2A) Gene Alterations

... Recent molecular studies have revealed that the genesis and pro gression of human cancer is largely attributed to accumulation of a series of genetic events that culminate in the transformation of a cell into a malignant clone (1). Central to this theory are the roles of oncogenes and tumor suppress ...
The Zebrafish Model Organism Database
The Zebrafish Model Organism Database

... record associated with specific experimental conditions. Information about Fish records (genotype, background, and STRs when applicable) can be found on ZFIN Fish record pages and in downloads files. Data from different model organism databases is currently annotated to records having varying degree ...
genetics of deafness
genetics of deafness

... important discovery, because the mutation in this gene is responsible for about 50% of nonsyndromic recessive deafness. The connexin 26 is a sub-unit that assembles with 5 other subunits to form a channel that connects one cell to the other and allows the passage of substances. It is possible to do ...
Gene regulation_1130(final)
Gene regulation_1130(final)

... • Insulin affects transcription, mRNA stability, and translation (from gene to protein) • Focusing on insulin-regulated gene transcription – Positive and negative effects on the transcription of specific genes even within the same cell. – Insulin-regulated genes  coding proteins involved in a varie ...
Neurofibromatosis Type 1
Neurofibromatosis Type 1

... about 360 kilobases with 60 exons, and unusual gene in that one of its introns contains coding sequences for at least three other genes. Neurofibromatosis Type 1 disease has been associated with over 500 different mutations in the NF1 gene and no single mutation is present in more than a few percent ...
Genetic Testing and Your Family
Genetic Testing and Your Family

... exists in multiple sperm or eggs (but not in other tissues of the parents, so their blood testing will be negative and they will not have features of CdLS), but are at risk (as high as 50 percent) to have other children with CdLS. In future pregnancies, serial ultrasound examinations may be performe ...
High Efficiency Transient Expression System for
High Efficiency Transient Expression System for

... Agrobacterium-mediated transient expression is a useful tool for assessing gene expression constructs in plants. It is rapid; typically giving results 2 to 3 days after inoculation, and has been demonstrated to work in whole leaf tissue from a range of plants including tobacco, potato and Arabidopsi ...
2007
2007

... the rII gene. How did they isolate the mutants? Is it a selection or screen? Answer: They plated the rIIB mutant FCO on E. coli K and looked for plaques. This is a selection because only revertants can grow on the K strain. c). (5 points) They found that the frequency of revertants was very high whe ...
Solid Tumour Section Thyroid: Papillary carcinoma with inv(7)(q21q34) in Oncology and Haematology
Solid Tumour Section Thyroid: Papillary carcinoma with inv(7)(q21q34) in Oncology and Haematology

... Note: Papillary carcinoma is a well-differentiated tumor of thyroid follicular cell origin and is the most common thyroid malignancy, constituting about 80% of all cases. The only known etiologic factor for this type of tumor is exposure to ionizing radiation, although the history of radiation expos ...
Extensions to Mendel`s Law
Extensions to Mendel`s Law

... Hypothesis 2 – one gene with incomplete dominance •OCA OCA (ocularcutaneous albanism) produces little or no pigmentation in skin,, hair,, and eyes. y •Can you determine the inheritance from pedigrees? ...
Package `BioQC`
Package `BioQC`

... A list of integer indices (starting from 1) indicating signature genes. Can be of length zero. Other data types (e.g. a list of numeric or logical vectors, or a numeric or logical vector) are coerced into such a list. See details below for a special case using GMT files. ...
Screening for homozygosity by descent in families with autosomal
Screening for homozygosity by descent in families with autosomal

... 1999; Pierce et al. 1999). We have employed the approach of screening for homozygosity by descent since the regions linked to the disease gene are almost certain to be homozygous in affected individuals of a family, and be common to all such members of the same family. The five cases that showed hom ...
Bayesian recursive mixed linear model for gene expression
Bayesian recursive mixed linear model for gene expression

... Genes with significant estimates for β3 indicates that ...
Investigation of the premelanosome protein
Investigation of the premelanosome protein

... cuniculus) has been the objective of pioneering studies on coat colour genetics. However, despite the early role of this species in defining genetic mechanisms determining this phenotypic trait, only recently a few loci have been characterized at the molecular level analysing also in rabbits genes a ...
Physiological and phylogenetic analysis of rhizobia isolated from
Physiological and phylogenetic analysis of rhizobia isolated from

... nifH1 and nifH2, and comparison with low range DNA ruler, 601 bp long amplified products were obtained (Figure 2). DISCUSSION The ability of legumes to obtain the nitrogen required for their growth and reproduction from both soil and symbiosis sets them apart from other economically valuable crops. ...
OVERALL MECHANISMS OF QUINOLONE RESISTANCE
OVERALL MECHANISMS OF QUINOLONE RESISTANCE

... • 11% QnrA+ isolates among ciprofloxacin-resistant K. pneumoniae and 0% in E.coli from USA [AAC (2004) 48: 1295] • 7.7% QnrA+ isolates among ciprofloxacin-resistant E. coli in Shanghai (China) [AAC (2003) 47: 2242] • 0.4% QnrA+ isolates among nalidixic acid- resistant Escherichia coli (France) [AAC ...
Evolution of Gene Expression
Evolution of Gene Expression

... still are) critical for establishing links between divergent gene expression and divergence of a particular phenotype; however, they are not suitable for obtaining the genomic measures of expression required to identify global trends in the evolution of gene expression. Rather, microarrays, which ar ...
Functomics!?
Functomics!?

... danger of propagation of incorrect functional information ...
Life: The Science of Biology, 10e
Life: The Science of Biology, 10e

BIBE2004Proteomics - Buffalo Ontology Site
BIBE2004Proteomics - Buffalo Ontology Site

... nuclear/cytoplasmic to regulate cell growth For a complete list of GO’s undefined terms and operators, see [18]. This lack of definitions and of rules for use of syntactic operators in the creation of compound terms leads to problems when GO is used for annotations of gene products, since such annot ...
Organismal lineages
Organismal lineages

... ex) rickettsias & mycobacteria= ostensible sister relationship (2-I,M aaRS) -But, same basic branching pattern -Same major taxonomic grouping within each domain as does the rRNA tree Consequently, aaRS trees cannot itself be the result of HGT An organismal gene trace is preserved in certain of the c ...
The Geographic Distribution of Monoamine Oxidase Haplotypes
The Geographic Distribution of Monoamine Oxidase Haplotypes

... To assess the population distribution of the five polymorphisms in the MAOA gene, we genotyped these positions in an additional set of DNA samples from 63 Caucasian, 33 Asian, and 40 African males. The eight haplotypes observed in this analysis and their frequencies in the tested populations are sum ...
Journal of Molecular Microbiology and Biotechnology
Journal of Molecular Microbiology and Biotechnology

... mycosubtilin biosynthesis gene cluster devoted to synthesis of an iturin-like compound, is situated at the same location [Duitman et al., 1999], suggesting that additional NRPS operons could be integrated in different ways in this area either as an insertion or as a substitution of existing NRPS ope ...
shERWOOD-UltramiR shRNA
shERWOOD-UltramiR shRNA

... Hannon Elledge (GIPZ) shRNA designs, the Hannon lab (Knott et al 2014) performed a large scale screen using each of these designs to target 2200 genes that were likely to impact growth and survival based on gene ontology. Inclusion as a hit required that at least 2 shRNA for that gene were depleted. ...
Genetic disorders of pigmentation - Zielinski Fam
Genetic disorders of pigmentation - Zielinski Fam

... melanosomes called bmacromelanosomes.Q These macromelanosomes are present in skin, iris, and retina. Ultrastructural analysis of the retinal pigment epithelium cells suggested that the giant melanosomes may form by abnormal growth of single melanosomes rather than by the fusion of several organelles ...
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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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