• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
Answers to End-of-Chapter Questions – Brooker et al ARIS site
Answers to End-of-Chapter Questions – Brooker et al ARIS site

... flowers and long pollen or red flowers and round pollen) was much higher than expected. Bateson and Punnett suggested that the gene controlling flower color were somehow coupled with the gene that controls pollen shape. This would explain why these traits did not always assort independently. Collabo ...
Worksheet complete this genetics problem practice
Worksheet complete this genetics problem practice

... The gene that controls whether or not a person can produce the pigment melanin which contributes to the color of skin, eyes and hair. Some people have the hereditary condition, albinism; they are not able to produce melanin and have little or no pigment in their skin and hair. Two different versions ...


... used to represent single copy regions within the genome (Solomon et al., 2006b; Solomon et al., 2006c). Genomic DNA from each of the strains was extracted using a Retsch MM301 autolyser and Qiagen BioSprint 15 and diluted to 6.7 ng μl-1, a concentration determined through template dilution experimen ...
American Berkshire Association
American Berkshire Association

... Seek-Gain: Litter Size – This is a group of porcine performance trait DNA marker tests utilizing information from two unique genes that impact litter size: Reproduction Rates ● Uterine Capacity. Gene Markers tested: ESR & EPOR. Seek-Gain: Animal Growth – This is a group of porcine performance trait ...
Bacterial speciation by sequencing of the 16S rRNA gene
Bacterial speciation by sequencing of the 16S rRNA gene

... Sequencing of the 16S rRNA gene from pathogens isolated at the University of Minnesota Veterinary Diagnostic Laboratory has been shown to be useful for speciation of bacterial isolates recovered from different animal species, as shown in Table 1. The new speciation method enabled the differentiation ...
Plant Development presentation
Plant Development presentation

... -Presentation: Introduction to Plant Development - Focus on Flower Development ...
Study Problems for Quiz 1
Study Problems for Quiz 1

... 1. A couple discovers that they are both heterozygous for the same two recessive disease states: cystic fibrosis and progeria (premature aging). The mutated genes are located on different autosomes. a. What is the probability that their first child will have one (either cystic fibrosis or progeria) ...
Who Is Right- DNA or Serology?
Who Is Right- DNA or Serology?

... • A blood center is using microarray to screen for rare donors • As part of their review process, the genotypes are checked against existing donor records • It is noted that several AfricanAmerican donors type as N negative by DNA but positive by serology ...
Leukaemia Section t(10;17)(p15;q21) ZMYND11/MBTD1 Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section t(10;17)(p15;q21) ZMYND11/MBTD1 Atlas of Genetics and Cytogenetics in Oncology and Haematology

... following diagnosis; (P2) died 37 months following the initial diagnosis. Another patient reported in the literature was in complete remission at 42 months after diagnosis. ...
Chapter 7 - Elsevier
Chapter 7 - Elsevier

... strains from an outbreak in France, 2006. Twelve case-patients and three isolates from cheese or raw milk processed in the incriminated plant (AFSSA SMVDXB0038-39-40) identified from epidemiologic analyses as the putative source shared the identical PFGE pattern (only patient strain XMON-1 is shown ...
kg3_9
kg3_9

... – For gaps 6 base or less on both mRNA and genome, just ignore gap, filling in with genome if necessary. – Try to turn other gaps into introns if they are not already by wiggling one base on either side of gap. – Break up alignments at remaining gaps that are not intronic. Intronic gaps are at least ...
Leukemia Section t(17;19)(q22;p13) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukemia Section t(17;19)(q22;p13) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... crossover between E2A intron 13 and HLF intron 3, type 2 from a crossover between E2A intron 12 and HLF intron 3 - t(17;19) type I: 5' E2A exons 1 to 13 <-> cryptic exon formed by E2A intron/HLF intron sequences to reestablish a reading frame <-> HLF exon 4 in 3' - t(17;19) type II: 5' E2A exons 1 t ...
Genetic Disorders as Models for Evolution
Genetic Disorders as Models for Evolution

... advantage in being a carrier. However, this would take a number of generations. [1] g) The mosquito that carriers the disorder is being controlled. Also, many North American Blacks may have migrated to areas where malaria doesn’t exist, breed out with other races, increased their gene pool. [1] h) ¼ ...
Document
Document

... 6.4 Traits, Genes, and Alleles Genes influence the development of traits. • The genome is the collection of all of an organism’s genetic material. – All of the genes on all of the chromosomes. • A genotype refers to the makeup of a specific set of genes. – the alleles of a specific gene – Bb, BB, b ...
Gene Section SEPT6 (septin 6) Atlas of Genetics and Cytogenetics
Gene Section SEPT6 (septin 6) Atlas of Genetics and Cytogenetics

... This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 2.0 France Licence. © 2003 Atlas of Genetics and Cytogenetics in Oncology and Haematology ...
Genetics and Heredity Outline
Genetics and Heredity Outline

...  Incomplete dominance or __________ inheritance occurs when the offspring shows traits that are a ______ or _____ of the two parents. Inheritance of Sex  Your ______ (male or female) was determined when your mother’s ____ was fertilized by your father’s _____.  Humans have one pair of chromosomes ...
PopulationGeneticsWorksheet.dot
PopulationGeneticsWorksheet.dot

... 1. In most populations, the frequency of two alleles is calculated from the proportion of homozygous recessives (q2), since it is the only identifiable genotype directly from its phenotype. If only the dominant phenotype is known, q2 may be calculated (1-frequency of dominant phenotype) . 2. All cal ...
Objective: To understand how Mendel used math to predict offspring
Objective: To understand how Mendel used math to predict offspring

... • Dominant- the gene which is expressed no matter what the other allele is. Represented by upper case symbol • Recessive- will be overshadowed in the presence of a dominant gene. 2 copies of a recessive allele must be present for the trait to show up. Represented by lower case symbol • There are som ...
autosomal inheritance
autosomal inheritance

... phenotypic splitting relation corresponds with genotypic splitting relation (1:2:1). ...
Assay Summary ATM Gene Mutation Analysis
Assay Summary ATM Gene Mutation Analysis

... ATM sequence: The mutation analysis will not detect mutations located in regions of the ATM gene that are not analyzed (non-coding exon regions, intron regions other than the splice junctions, and upstream and downstream regions). The method also will not detect gross genetic alterations including d ...
Test Information Sheet HEXA Gene Analysis in Tay
Test Information Sheet HEXA Gene Analysis in Tay

mendel II
mendel II

... • As an example, the enzyme "phosphatase" removes phosphate groups from other molecules. When an extract is made of the proteins in an organism, it is possible to separate the proteins by electrophoresis and then stain the gel so only the phosphatase will appear. • In this example, there are 2 allel ...
PowerPoint 프레젠테이션
PowerPoint 프레젠테이션

... The signaling pathway for activation of the drosophila DL morphogen parallels a mammalian signaling pathway for activation of NK-kB ...
HGT as a force creating new pathways
HGT as a force creating new pathways

... What is it good for? Gene duplication events can provide an outgroup that allows rooting a molecular phylogeny. Most famously this principle was applied in case of the tree of life – the only outgroup available in this case are ancient paralogs (see http://gogarten.uconn.edu/cvs/Publ_Pres.htm for m ...
Leukaemia Section t(5;14)(q33;q24) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section t(5;14)(q33;q24) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... them compatible with the molecular breakpoint found. (C) FISH painting using STAR*FISH human whole chromosome specific probes for chromosomes 5 (Cy3, red) and 14 (FITC, green) which confirms the translocation between them. ...
< 1 ... 240 241 242 243 244 245 246 247 248 ... 392 >

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.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report