• Study Resource
  • Explore
    • 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
Fulltext PDF - Indian Academy of Sciences
Fulltext PDF - Indian Academy of Sciences

... Origin and roles of DNA methylation patterns mutations and various types of extended addition–deletion mutations). Sites of cytosine methylations are themselves hotspots for occurrence of mutations. The cytosine methylation and histone modification marks amplify the genetic variation manifold epigen ...
MHF1 plays Fanconi anaemia complementation group M protein
MHF1 plays Fanconi anaemia complementation group M protein

... (a) The sequence of the 50 end of the transcript, containing the start codon ATG (highlighted in blue) was determined by 50 RACE PCR (rapid amplification of cDNA ends, polymerase chain reaction) analysis. The N-terminal sequence of the protein is displayed under the coding sequence. (b) AtMHF1 is lo ...
operon
operon

... Anabolic Pathways and End-Product Repression • For anabolic pathways, the amount of enzyme produced by a cell usually correlates inversely with the concentration of the end product of the pathway • E.g., as the concentration of tryptophan rises, it is efficient for the cell to reduce the production ...
Genes Involved in Sister Chromatid Separation and Segregation in
Genes Involved in Sister Chromatid Separation and Segregation in

... mutants that contain a GFP-marked chromosome. Nine LOC (loss of cohesion) complementation groups that do not segregate sister chromatids at anaphase were identified. We cloned the corresponding genes and performed secondary tests to determine their function in chromosome behavior. We determined that ...
Power Point
Power Point

Identification of New Genes Involved in Meiosis by a Genetic Screen
Identification of New Genes Involved in Meiosis by a Genetic Screen

... Budding yeast Saccharomyces cerevisiae contains a group of proteins named ZMM that constitutes a link between recombination and Synaptonemal Complex (SC) assembly. Yeast mutants that lack ZMM proteins have defects in recombination, SC formation and nuclear division progression. Meiotic cell cycle pr ...
animal genetics
animal genetics

... A punnett square is a grid-like method that is used to display and predict the genotypes and phenotypes of offspring from parents with specific alleles. Illustration of DNA Double Helix from Wikipedia. ...
You Light Up My Life
You Light Up My Life

... Genotype & Phenotype • Genotype refers to particular genes an individual carries • Phenotype refers to an individual’s observable traits • Cannot always determine genotype by ...
Association genetics of complex traits in conifers
Association genetics of complex traits in conifers

... reason they will have extended linkage disequilibrium around the mutation [24]. In common diseases, the underlying loci might have smaller effects, and the alleles might be older [22,23]. Plant breeders are interested in genes that have been under strong selection during domestication, such as flowe ...
Analysis of Drosophila Species Genome Size and Satellite DNA
Analysis of Drosophila Species Genome Size and Satellite DNA

The Answer Is Fifteen Percent - CHEST Journal
The Answer Is Fifteen Percent - CHEST Journal

... emphysema.9 Other antiproteases that have been studied include ␣1-antichymotrypsin, ␣2-macroglobulin, secretory leukocyte protease inhibitor, elafin, and tissue inhibitors of metalloproteases.6,7 Macrophage-derived proteases such as the cathepsins and matrix metalloproteases have received some atten ...
Friedreich ataxia: The clinical picture
Friedreich ataxia: The clinical picture

... the level of residual frataxin expression, it has an influence on the severity of the phenotype. A direct correlation has been firmly established between the size of the GAA repeat and an earlier age of onset, an earlier age of confinement to a wheelchair, more rapid rate of disease progression, car ...
Pet_SUMO manual
Pet_SUMO manual

Accelerated Evolution of Sex Chromosomes in
Accelerated Evolution of Sex Chromosomes in

alignment-2005
alignment-2005

... can be more informative than DNA • protein is more informative (20 vs 4 characters); many amino acids share related biophysical properties • codons are degenerate: changes in the third position often do not alter the amino acid that is specified CGX codes for ARG (Arginine) where X is one of AGCT • ...
Meiosis I
Meiosis I

... Phases of Meiosis • Meiosis - process in which the number of chromosomes in a diploid cell is cut in half. • Made up of meiosis I and meiosis II. • By the end of meiosis II, the diploid cell becomes four haploid cells. ...
1 - SACE
1 - SACE

... This means that the male is from one breed and the female is from another breed so that their offspring have a mixture of characteristics from each parent. An example is when a variety of wheat with high yield is crossed with a variety that is rust resistant then the offspring might have high yield ...
natural transformation increases the rate of adaptation in the human
natural transformation increases the rate of adaptation in the human

... and the experimental strain (Travisano and Lenski 1996). Selection rate compared to the control strain was calculated for each experimental strain and ancestor in this assay. This measurement represents the difference between the natural logarithm of population growth rates for each experimental lin ...
Let`s see How Dramatic Effect can be drawn by Point Mutation with
Let`s see How Dramatic Effect can be drawn by Point Mutation with

... U is inserted between two G and the frame is changed. The new codons made by insertion are matched to some materials that give dramatic effect. Change of reading frame ...
Association of estrogen receptor β gene polymorphisms with bulimic
Association of estrogen receptor β gene polymorphisms with bulimic

... variants for this group of bulimic women. Identification of novel variants of the ERb gene The association described above could exist either because changes at the nucleotide positions in question affect ERb function or because they are in linkage disequilibrium with functional changes that might o ...
the loci of evolution: how predictable is genetic
the loci of evolution: how predictable is genetic

... which alter the amino-acid sequence or the mature RNA nucleotide sequence; (2) cis-regulatory changes, which alter gene expression; and (3) genetic changes that alter both the coding and the cis-regulatory regions of one or several gene(s) (gene loss, gene duplication, gene rearrangement, etc.). Cod ...
Leukaemia Section T-lineage acute lymphoblastic leukemia (T-ALL) Atlas of Genetics and Cytogenetics
Leukaemia Section T-lineage acute lymphoblastic leukemia (T-ALL) Atlas of Genetics and Cytogenetics

... chromosomal abnormalities affecting 7q34 (TRB@) occur in 5% to 8% of T-ALL cases with an abnormal karyotype. Recent molecular cytogenetics studies have revealed a higher incidence of TRB@ locus rearrangements (about 20% of all T-ALL cases). This finding demonstrates that the frequency of TRB@ rearra ...
Physical Models for Protein Folding and Drug Design
Physical Models for Protein Folding and Drug Design

The Origin of the Genetic Code
The Origin of the Genetic Code

... The main features, which have frequently been commented on, are: (4) The 20 amino acids are not distributed at random among the 64 triplets. In fact, several rules can easily be deduced from the Table. For example, (a) XYU and XYC always code the same amino acid. (b) XYA and XYG often code the same ...
Technical Summary - Office of the Gene Technology Regulator
Technical Summary - Office of the Gene Technology Regulator

...  widespread presence of the same or similar proteins encoded by the introduced genes in the environment and lack of known toxicity or evidence of harm from them. The identified risk was assessed in comparison to the parent non-GM white clover, also taking into account, intended agronomic management ...
< 1 ... 202 203 204 205 206 207 208 209 210 ... 2254 >

Artificial gene synthesis

Artificial gene synthesis is a method in synthetic biology that is used to create artificial genes in the laboratory. Currently based on solid-phase DNA synthesis, it differs from molecular cloning and polymerase chain reaction (PCR) in that the user does not have to begin with preexisting DNA sequences. Therefore, it is possible to make a completely synthetic double-stranded DNA molecule with no apparent limits on either nucleotide sequence or size. The method has been used to generate functional bacterial or yeast chromosomes containing approximately one million base pairs. Recent research also suggests the possibility of creating novel nucleobase pairs in addition to the two base pairs in nature, which could greatly expand the possibility of expanding the genetic code.Synthesis of the first complete gene, a yeast tRNA, was demonstrated by Har Gobind Khorana and coworkers in 1972. Synthesis of the first peptide- and protein-coding genes was performed in the laboratories of Herbert Boyer and Alexander Markham, respectively.Commercial gene synthesis services are now available from numerous companies worldwide, some of which have built their business model around this task. Current gene synthesis approaches are most often based on a combination of organic chemistry and molecular biological techniques and entire genes may be synthesized ""de novo"", without the need for precursor template DNA. Gene synthesis has become an important tool in many fields of recombinant DNA technology including heterologous gene expression, vaccine development, gene therapy and molecular engineering. The synthesis of nucleic acid sequences is often more economical than classical cloning and mutagenesis procedures.
  • studyres.com © 2025
  • DMCA
  • Privacy
  • Terms
  • Report