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Evolution
Evolution

... successfully mapped the genomes of other species, including the fruit fly, mouse, and Escherichia coli. The location and complete sequence of the genes in each of these species are available for anyone in the world to access via the Internet. Why is this information important? Being able to identify ...
Search - VectorBase
Search - VectorBase

... or by the number of hits. Click on the ​plus sign to show or hide categories (available options depend on which Domain you have selected). ...
Down syndrome is caused by trisomy 21
Down syndrome is caused by trisomy 21

... Down Syndrome and Translocation Heterozygote • Down syndrome is caused by trisomy 21 (3 copies of chromosome 21). • 95% of Down syndrome cases are associated with nondisjunction and shows no familial recurrence. ...
Molecular Genetics of Inherited Disorders
Molecular Genetics of Inherited Disorders

... Figure 1. The basic structural features of a gene and steps for its expression. A gene is composed of two major parts, a sequence transcribed into RNA and sequences not transcribed but which is necessary for the expression of the gene activity. The transcribed sequence can be further subdivided into ...
Readme file describing the networks/expression data
Readme file describing the networks/expression data

... In this directory you can download various data associated with the PlaNet database. Description of the files: -CelFileID.zip contains names of the cel files used to construct the PlaNet database. -PlaNetStandalone.zip: Stand-alone version of PlaNet implemented in Python. In addition, expression dat ...
``Best Friends`` Sharing the HMGA1 Gene: Comparison of the Human
``Best Friends`` Sharing the HMGA1 Gene: Comparison of the Human

... of which SPV1 and SPV2 are the commonly found variants. The characterized dog variants showed the same composition structure as the mentioned human variants SPV1 and SPV2. Canine counterparts of the human transcript variants SPV3–SPV7 could not be detected using polymerase chain reaction (PCR) ampli ...
Module 3: Genes and Sequences (NCBI)
Module 3: Genes and Sequences (NCBI)

... record. On the BLink page you can view a blast2 alignment between your protein and each protein identified by BLink as highly similar. Scroll down the list of Protein Descriptions to view the protein names for these proteins. Homologs can also be identified through cross-species BLAST searches, as d ...
Gene therapy - A sustainable approach to health?
Gene therapy - A sustainable approach to health?

... and scientific problems remain unsolved. Some of the necessary research that should have been done long ago is only now being carried out, revealing findings that confirm our worst fears. The NIH’s 1995 expert panel’s report documents a plethora of scientific and clinical risks associated with gene ...
PDF
PDF

... When conducting genetics research, whether from the perspective of a candidate gene study or genome wide association study (GWAS), researchers must be able to accurately identify and translate where molecular markers are located on the genome in reference to the coordinates of known genes. While thi ...
To narrow a gene pool is dangerous
To narrow a gene pool is dangerous

... What we should understand about gene pools. Sadly, some scientists are quite indifferent to the serious consequences that can result when a gene pool has been stripped of its integrity. Gene pool is a term often bandied about, but few people have any idea of the dangerous implications of a narrowly ...
Introduction to Special Issue: A New Paradigm of Gene Therapy
Introduction to Special Issue: A New Paradigm of Gene Therapy

... The delivery systems of nucleic acids are particularly important, and in this issue we have many studies related to this issue using cationic lipids [3,4], polymers [5–7], and functional peptides [8,9]. As is well known, there is a long history of developing effective delivery systems from various f ...
Integrated Teaching Area (ITA) Scenarios for Semester One
Integrated Teaching Area (ITA) Scenarios for Semester One

... forget to discuss formation of chiasmata and crossing over. How can two genes on the same chromosome segregate independently (as described by Mendel’s first law)? Crossing over at meiosis. Two loci close together on one chromosome may segregate together as crossing over is less likely to happen betw ...
Dihybrid Crosses Gregor Mendel, the father of modern genetics
Dihybrid Crosses Gregor Mendel, the father of modern genetics

... You are a geneticist working for a large seed company. One of your colleagues is fired before she can finish some important experiments she was working on. The company president has turned the project over to you. All you know is that your former colleague was working with a rare type of flower that ...
Gene expression pipelining, applications and the wisdom
Gene expression pipelining, applications and the wisdom

Genetics and Insurance: An Actuary's View
Genetics and Insurance: An Actuary's View

...  Novel mechanisms (epigenetics, RNA interference)  Genetic therapy ...
other_patterns_of_inheritance
other_patterns_of_inheritance

... fur (Xb). The orange allele is dominant to the black allele. Ordinarily, this would mean that an animal inheriting one copy of each gene should have orange fur. However, a heterozygous female cat (XBXb) will not be orange. Instead, her coat will be a patchwork of orange and black, a condition known ...
Diapositiva 1
Diapositiva 1

... fact, that is not the case. – Part of the problem is due to the fact that it is hard to predict gene structure (intron/exon) without knowing the entire mRNA sequence, which happens for about two-thirds of all genes. – Then, there are errors in the assembly (putting together the sequence snippets). A ...
Genetics: Mendelian Genetics (2) Patterns of Inheritance
Genetics: Mendelian Genetics (2) Patterns of Inheritance

... One type of dwarfism in humans is caused by a single dominant gene; the condition is called Achondroplastic dwarfism. Dwarf individuals are heterozygous, while persons who are homozygous recessive are of normal stature. The homozygous dominant individuals all die before birth. (20% family history, a ...
One Size Fits All: Can the Cure for Severe Combined Immunodeficiency X-linked Also Work for SCID due to Adenosine Deaminase Deficiency?
One Size Fits All: Can the Cure for Severe Combined Immunodeficiency X-linked Also Work for SCID due to Adenosine Deaminase Deficiency?

... There are several types of Severe Combined Immunodeficiency (SCID), and Adenosine deaminase (ADA) deficiency is the cause of only portion of all SCID cases. The most common form is SCID X-linked, which is caused by a mutation on the X chromosome, and affects only males. SCID-ADA is an autosomal rece ...
Article - Nature
Article - Nature

... PhzH-Pa,5 and PhzH-Pc6 had been evaluated for their function in secondary metabolite syntheses in vivo. Only NspN2 and PcsB6 had also been characterized in vitro. In contrast, ORF5,8 SioC, ORF1,9 SfaP, TcsG, FdmV,10 SanV,11 and LlpA12 had not yet been fully characterized. Their involvement in second ...
Evolution Big Idea 1 Investigation 3 BLAST lab
Evolution Big Idea 1 Investigation 3 BLAST lab

... analyze biological data. Comparative genomics involves the use of computer programs that can line up multiple genomes and look for regions of similarity among them. Using bioinformatics methods, entire genomes can be quickly compared in order to detect genetic similarities and differences. Some of t ...
Albinism Poster - Harlem Children Society
Albinism Poster - Harlem Children Society

... Acknowledgements: Bronx Community College, National Science Foundation, BCC and CCNY of CUNY, Harlem Children Society, Dr. Brennan, Dr. Sat, Ms. McMahon , Bronx Health Sciences High School ...
No Slide Title
No Slide Title

... -implant embryos back in mothers. -gene will be incorporated into genome and expressed in some but not all baby mice, -produced 2 XX male mice. These were Sry transgenic but also sterile (because lacked other missing Y genes.) ...
Gene Section GRB10 (growth factor receptor-bound protein 10) in Oncology and Haematology
Gene Section GRB10 (growth factor receptor-bound protein 10) in Oncology and Haematology

... JAK2, BCR-Abl TEC kinase, NEDD4, cABL, AKT, cKIT). Several studies suggest a role for Grb10 in cell proliferation. However, despite the clear involvement of Grb10 in pathways activated by IR and IGF-R, there is still some controversy about whether its effect is inhibitory or stimulatory. One report ...
DNA snorks
DNA snorks

... Introduction: In this simulation, you will examine the DNA sequence of a fictitious organism the Snork. Snorks were discovered on the planet Dee Enae in a distant solar system. Snorks only have one chromosome with eight genes on it. Your job is to analyze the genes of its DNA and determine what trai ...
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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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