• 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
Observable Patterns of Inheritance Earlobe Variation Early Ideas
Observable Patterns of Inheritance Earlobe Variation Early Ideas

... • Two alleles (IA and IB) are codominant ...
University of Groningen Characterisation of actinomycete
University of Groningen Characterisation of actinomycete

... After assembling all DNA sequences from pMEA100, we obtained 1 final contig of 23290 bp. Sequencing primers were used to bridge the BamHI sites used in the subcloning. This revealed an additional BamHI (12832 bp) site at only 24 bp of the previously identified BamHI (12808 bp) site, which was not de ...
The Neurospora crassa colonial temperature
The Neurospora crassa colonial temperature

... We cloned the three genes by complementation (Davis 2000), utilizing the Orbach/Sachs N. crassa genomic DNA cosmid library (Orbach and Sachs 1991). The cot-2 and cot-4 genes are unlinked. However, as both genes reside on linkage group V (Perkins et al. 2001) the same complementation strategy was emp ...
IJBT 11(2) 220-223
IJBT 11(2) 220-223

... step PCR or two step nested-PCR under low stringent condition, indicating the presence of at least two DRB genes. Presence of multi DRB genes (3) was also reported by Schwaiger et al9. The existence of several DRB genes in other artiodactyla species reinforces this hypothesis. However, in present st ...
The genetics of cystic fibrosis
The genetics of cystic fibrosis

... CFTR gene gives rise to a very variable phenotype (clinical picture) that may not be predictable from the individual’s genotype (gene mutation). It is believed that environmental factors and the influence of other modulator genes affect the ability of the CFTR genes to express their full disease pot ...
National Center for Biotechnology Information (NCBI)
National Center for Biotechnology Information (NCBI)

... 2. The second section (Descriptions) lists the name of the sequence and the Score and E value (the higher the score and the lower the E value the better.) There are also links back to the protein record on the right. 3. The third section (Alignments) compares your sequence with each answer. Each ans ...
Balancing Redox Cofactor Generation and ATP Synthesis: Key
Balancing Redox Cofactor Generation and ATP Synthesis: Key

... objection to the large scale production of ethanol via such methods is that the fermentative substrates generally originate from foodstuffs such as maize and sugarcane. The use of alternative nonfood grade carbon feedstocks, principally lignocellulose, has received considerable attention over the la ...
Cavy Genetics - British Cavy Council
Cavy Genetics - British Cavy Council

... many different varieties of cavy arise or which new ones may be possible, then hopefully it will be of interest. It should also give you a better understanding about why some ‘unexpected’ things sometimes happen in matings (e.g. why Rex bred to Teddies produce smooth-hairs), or why there is such a t ...
Ribosome reinitiation at leader peptides increases translation of
Ribosome reinitiation at leader peptides increases translation of

... No attempt to confront the observed distance between leader genes and downstream genes and the observed distance in known operons has been made. In Escherichia coli the distance between two consecutive genes peaks at around 10 nt. While it might support authors’ hypothesis (and there is a glimpse of ...
Understanding the Genetics of HHT
Understanding the Genetics of HHT

... What is the chance a dominant genetic disorder, like HHT, will get passed on to children? Since individuals with HHT actually have two copies of the “HHT gene”—one normal and one abnormal— each of their children has a 50% (1/2) chance of having HHT. This is because each egg and sperm has only one c ...
CorrelateTalk
CorrelateTalk

... For the statisticians: the penalties maximizeu,v u’XY’v subject to u’u ≤ 1, v’v ≤ 1, P1(u) ≤ c1, P2(v) ≤ c2 If P1 is a lasso or L1 penalty, P1(u)=||u||1, then to update u: u=S(XY’v, d)/||S(XY’v,d)||2, where d≥0 is chosen such that ||u||1=c1. Here, S is the soft-thresholding operator: S(a,c)=sign(a) ...
Chapter 19: Human Genetics
Chapter 19: Human Genetics

... XX egg + Y sperm = Klinefelter syndrome no X egg + X sperm = Turner syndrome 19. If one parent has only dominant genes and the other has only recessive genes for a particular recessive genetic disorder, how many of their children should be affected by the disorder? Ans: None, all of the children wou ...
Complementation Help - Biological Sciences
Complementation Help - Biological Sciences

... In Haploid species (e.g. yeast) ...
Chapter 19: Human Genetics
Chapter 19: Human Genetics

... XX egg + Y sperm = Klinefelter syndrome no X egg + X sperm = Turner syndrome 19. If one parent has only dominant genes and the other has only recessive genes for a particular recessive genetic disorder, how many of their children should be affected by the disorder? Ans: None, all of the children wou ...
IMSR File Format
IMSR File Format

... Undifferentiated cells derived from blastocyst-stage embryos. ES cells can differentiate in culture to a number of different cell types. When incorporated into chimeric mouse embryos they are totipotent and can differentiate into any cell type in the mouse. If these cells become part of the germline ...
Genetic Characterization of Insulin Growth Factor
Genetic Characterization of Insulin Growth Factor

... Based on the chromosome homology between cattle and river buffalo, we expect IGF-1 gene to be located on the long arm of buffalo chromosome 4 (4q) which resulted from the centric fusion between two acrocentric cattle chromosomes nos. 5 and 28 [15]. Transcripts derived from exons 1 and 2 are alternat ...
Cowboy Genetics
Cowboy Genetics

... PHA carrier cows bred to a PHA carrier bull, you would have 25 PHA calves, 50 PHA carriers and 25 normal calves. That would be a heck of a financial loss! Wouldn’t it be nice to know if your animal was a carrier before you bred them? If gene hunting goes well, we may have a test by the time this art ...
Gene Section MAP2 (microtubule associated protein 2) -
Gene Section MAP2 (microtubule associated protein 2) -

... neuronal cells, it induced the rearrangement of the microtubules into long bundles. These bundles enabled outgrowths from the non neuronal cells. Experiments done with knockout mice show that the role of MAP2 in neuronal morphogenesis may be redundant (Teng et al., 2001). Single knockouts of MAP2 di ...
Slide 1
Slide 1

... contribute to this association4. Genetic studies in several populations have identified a region on chromosome 5q31-q33 that contains the asthma susceptibility gene in several populations5,6,7,8. This region contains a cluster of pro-inflammatory cytokines genes that play an important role in immune ...
a code for traits: dna structure and function
a code for traits: dna structure and function

...  a description of how siblings can inherit different DNA  a brief description of DNA structure and how one person’s DNA is different from another’s  a discussion of how DNA is a code for traits  independent assortment and crossing over during meiosis ...
Hulmi, Finland: Enhancing Muscle Mass and Function
Hulmi, Finland: Enhancing Muscle Mass and Function

... 20 wk weekly injections ...
How many genes in Arabidopsis come from cyanobacteria? An
How many genes in Arabidopsis come from cyanobacteria? An

... plastids? If so, they should branch with the yeast homologue, the only other eukaryote in our sample. A glance at the summary of the BLAST results showing the numbers of times that the best hit with the Arabidopsis query was found in a particular genome at three expectation thresholds reveals that y ...
Read PDF - Hormones
Read PDF - Hormones

... surrounding them is increased. Large, abnormal cytoplasmic vacuoles containing bone collagen fibrils were observed by ultrastructural examination. The conclusion is that although pycnodysostosis osteoclasts function normally in demineralizing bone, they do not adequately degrade the organic matrix. ...
Linkage and Recombination
Linkage and Recombination

... determined the difference between two or more alternative phenotypes. • Different genes controlled different aspects of phenotype. Gene = unit of function. • Mutation changed one allele to another. Gene = unit of mutation • Different genes could be separated by recombination. Gene = unit of recombin ...
Chapter 16 Other RNA Processing Events
Chapter 16 Other RNA Processing Events

... In mice there are 4 Ago genes but only Ago2 appears to be SLICER. ...
< 1 ... 106 107 108 109 110 111 112 113 114 ... 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