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DROSOPHILA MELANOGASTER - THE MODEL ORGANISM OF
DROSOPHILA MELANOGASTER - THE MODEL ORGANISM OF

... tools evolved from these studies have placed Drosophila in its unparalleled position in terms of understanding gene/protein function. In particular, two types of special chromosomes were developed as result of their work. Balancer chromosomes were first created by Muller (18). These chromosomes with ...
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L-Lysin-Production with Corynebacterium glutamicum
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... Several genes or a portion of the chromosome ...
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Protein Structure Prediction
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PPT - Blumberg Lab
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Probability Rules
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... 1. Sam Fitzgerald is a carpet salesman who at age 46 beings to slur his speech and stagger slightly when we walks. His speech worsens, he develops a shuffling gait to avoid falling and he loses his job when customers complain. His children urge him to seek counseling and after testing, he learns tha ...
18.3 Amino Acids - Haverford Alchemy
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Bioinformatics: Molecular Computational Tools (Module II)
Bioinformatics: Molecular Computational Tools (Module II)

... molecular biologist. A number of computational programs are available that help search through genome databases, design primers for PCR, translate a DNA sequence into an amino acid sequence (and vice versa), identify conserved regions in the amino acid sequence (domains), etc. In this lab, you will ...
bioinformatics module ii - Tetrahymena Genome Database
bioinformatics module ii - Tetrahymena Genome Database

... molecular biologist. A number of computational programs are available that help search through genome databases, design primers for PCR, translate a DNA sequence into an amino acid sequence (and vice versa), identify conserved regions in the amino acid sequence (domains), etc. In this lab, you will ...
Alzheimer`s Disease Genetics
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... each biological parent. This combination is one factor among many that influence a variety of processes in the body. On chromosome 19, the apolipoprotein E (APOE) gene has three common alleles: 2, 3, and 4. ■ Apolipoprotein E (APOE) gene—A gene on chromosome 19 involved in making a protein that h ...
Simple Models of Protein Folding
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... effects, which may be even more important in three dimensions. However, short proteins in two dimensions do maintain a surface-to-volume ratio similar to long proteins in three dimensions [1]. Furthermore, the simplicity of two dimensions allows an exact characterization of short polymer sequences. ...
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... separate it into multiple tubes. 2) Cut large gel slices into several pieces to accelerate the gel dissolution. 3) Extend the incubation time to completely dissolve the gel slice. ...
Bacterial plasmid transformation is a commonly employed technique
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... any of the other transformations. The difference that exists in colony number between the pBR322 and pUC19 transformations might be attributed in part to the concentrations of plasmid used, as the concentrations were determined by OD260/280, the concentrations reflect the number of base pairs, but n ...
(HbA) and sickle hemoglobin
(HbA) and sickle hemoglobin

... Many changes in the structure of hemoglobin have arisen by mutations in the human population. About one person in 100 contains a mutant hemoglobin gene and these individuals have an abnormal hemoglobin molecule in their blood. The mutations often involve substitution of one amino acid for another an ...
Molecular Cloning, Sequencing, and Expression of the Glutamine
Molecular Cloning, Sequencing, and Expression of the Glutamine

... to the GTG start codon. Two TGA stop codons separated by a single alanine codon were found in-frame beginning at position 1057 downstream from the start. GS requires ATP for its activity. The putative ATP- ...
Dravets_LETM1 - Medicinal Genomics
Dravets_LETM1 - Medicinal Genomics

... anchor proteins, might be responsible. Recent studies on animal models showed that alterations in the biogenesis of GPI anchor proteins can alter expression of Nav1.1 encoded by SCN1A [21] gene. As epilepsy is such a variable disorder that can present itself in different types and different phenotyp ...
AnnotatorsInterface-GUS
AnnotatorsInterface-GUS

... Toggle (or configure) the display of each feature type Zoom to sequence level and will include links to functionality relevant to the feature highlighted Also support creation of features “from scratch” – based on literature, etc. ...
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Point mutation



A point mutation, or single base modification, is a type of mutation that causes a single nucleotide base change, insertion, or deletion of the genetic material, DNA or RNA. The term frameshift mutation indicates the addition or deletion of a base pair. A point mutant is an individual that is affected by a point mutation.Repeat induced point mutations are recurring point mutations, discussed below.
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