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Domains of group A streptococcal M protein that confer resistance to
Domains of group A streptococcal M protein that confer resistance to

... The M-protein family is extensive in group A streptococcus and exhibits a diverse range of antigenic and functional properties. The study of Sandin et al. on M5 protein should be extended to other members of the M-protein family that interact with other human proteins. Such studies might also be bro ...
Structure and functions of lampbrush chromosomes
Structure and functions of lampbrush chromosomes

... et al., 2009). They can also undergo seasonal changes (Tsvetkov and Parfenov, 1994). This is particularly evident in hibernating amphibians. During the summer, when the animals are the most active, the transcriptional activity of LBCs is the highest, as well. In the autumn, LBCs’ activity abates. Ne ...
3.6 Genetics pp - 7th-grade-science-mississippi-2010
3.6 Genetics pp - 7th-grade-science-mississippi-2010

... • The offspring of asexual reproduction are a)Identical to the parent organism b)Similar to a parent organism c)A combination of two parent organisms d)Prokaryotic ...
Direct Sequence Analysis of the 14q+ and 18q
Direct Sequence Analysis of the 14q+ and 18q

... requires the presence of the 5' recombination signals next to the junctional D, exon, lack of amplification may be due to removal of the 5' recombination signal sequence by a preceding V,-D, recombination. In addition, the D, primer includes part of the intervening sequence between the heptamer and ...
p53 gene mutation: software and database
p53 gene mutation: software and database

... involved in both monogenic and polygenic disorders, including complex diseases such as cancer (1). Furthermore, for each of these genes, numerous and varied types of alterations have been described, ranging from point mutations to large deletions. A record of the mutations in these various genes ser ...
Construction of the optimal single gene ranking
Construction of the optimal single gene ranking

... for use as a control (since overly random). We used SVM as a binary classifier, but node degree provides a ranked list of genes. In our use of GeneMANIA, this ranked list of genes can be directly compared to the ranked list of genes provided by the algorithm. Thus, our prediction is identical regard ...
PANTHER version 11: expanded annotation data from Gene
PANTHER version 11: expanded annotation data from Gene

... been annotating PANTHER trees with GO terms since 2011, and is now the single largest contributor of manuallyreviewed GO annotations in the GO Consortium (12). The GO Phylogenetic Annotations for individual genes are also available directly from the GO website, but they are used differently on the P ...
Lesson Plan
Lesson Plan

... A. A cell is a basic unit of life containing living material bound by a membrane. The cell also contains genetic material. 1. Within each cell there is a nucleus that contains genetic material. 2. The long molecule that carries the genetic material is DNA or deoxyribonucleic acid. 3. The DNA is orga ...
PPT3 - Ycmou
PPT3 - Ycmou

chapter 12 lecture slides
chapter 12 lecture slides

... • Refers to an allele which has more than one effect on the phenotype • Pleiotropic effects are difficult to predict, because a gene that affects one trait often performs other, unknown functions • This can be seen in human diseases such as cystic fibrosis or sickle cell anemia – Multiple symptoms c ...
B1 SHA - you and your genes
B1 SHA - you and your genes

... True of False • Chromosomes are found in the nucleus. • Sperm and egg cells have the same amount of information as other body cells. • When we are adults our cells stop dividing. • Everyone in this room in unique. • Genes are joined up into chains called chromosomes. • The environment we grow up in ...
chapt12_lecture from text
chapt12_lecture from text

... • Refers to an allele which has more than one effect on the phenotype • Pleiotropic effects are difficult to predict, because a gene that affects one trait often performs other, unknown functions • This can be seen in human diseases such as cystic fibrosis or sickle cell anemia – Multiple symptoms c ...
order code
order code

... Methyl-CpG-binding protein 2 (MeCP2), as the main cause of RTT. MECP2 mutations have also been found in females with atypical RTT and in males with severe neonatal encephalopathy, as well as in patients with clinical features of Angelman syndrome, Klinefelter syndrome, autism, mental retardation, re ...
Mutation
Mutation

... Common; A or G are removed and replaced with a random base. Deamination Amino group is removed from a base (C  U); if not replaced U pairs with A in next round of replication (CG  TA). ...
Chapter 8
Chapter 8

... © 2016 Pearson Education, Inc. ...
Molecular biology of brain aging and neurodegenerative disorders
Molecular biology of brain aging and neurodegenerative disorders

... hypothetical threshold necessary for indefinite survival; hence, aging is an evolutionary necessity. To account for the known genetic influences on longevity, one would expect the existence of genes which may regulate the amount of cellular energy devoted to repair of free radical damage, protein tr ...
Tumors with microsatellite instability: many mutations, targets and
Tumors with microsatellite instability: many mutations, targets and

... some or all of the MSI-positive tumors. Therefore, these studies fall under the old maxim that if observations rely on statistical validation, it would suggest an urgent need to perform a better experiment. Of course, there is the argument that the approach formally forbids the conclusion that genes ...
The Classical Genetic Switch in Lambda Phage- Lysis and
The Classical Genetic Switch in Lambda Phage- Lysis and

... In order to understand how switching happens between the lysis and lysogeny states in the lambda phage, we focus on two regulatory genes CI and cro and a regulatory region OR called the right operator as shown in Fig 3. During the lysogeny phase CI is switched ON and cro is OFF. The operator OR is c ...
Whole_exome sequencing of 228 patients with sporadic Parkinson`s
Whole_exome sequencing of 228 patients with sporadic Parkinson`s

... drawn from the UK10K 16 study. We performed association tests both at the level of single-nucleotide variants and at the gene level but found that no variant was significantly associated with PD after applying a multiple-testing correction. While power for discovery is clearly the major issue, there ...
Abstract - American Life Science Pharmaceuticals
Abstract - American Life Science Pharmaceuticals

... validation of new drug targets and demonstration that compounds directed to such targets are efficacious in TBI animal models using clinically relevant methods. The cysteine protease cathepsin B has been implicated in mediating TBI, but it has not been validated by gene knockout studies. This invest ...
Integrative omics in Expression Atlas
Integrative omics in Expression Atlas

... ID mapping from gene to other entities ...
PDF
PDF

... minutes at 72°C to complete a cycle and cycle was repeated for 34 times. The final extension duration was 7 minutes at 72°C. then, PCR products were mixed with 3 µl of 2X gel loading dye. Polymorphisms in the PCR products were analyzed by electrophoresis using mini vertical polyacrylamide gels for h ...
NTP Activities for the National Children’s Study Funding Redirect
NTP Activities for the National Children’s Study Funding Redirect

... Biomolecular Screening Branch: Development of a HTSTranscriptomics Platform • Goal: Conduct targeted transcriptomic interrogation of human, mouse, rat, and zebrafish cellular lysates – Develop a mid- to high- throughput transcriptomics technology for measuring the expression levels of a set of ~2500 ...
Autosomal Recessive Disorders
Autosomal Recessive Disorders

... genes coding for a particular trait are located at particular positions on chromosomes-loci come in several forms-alleles receive one allele from each parent if identical-homozygous for a trait if different-heterozygous recessive traits are not expressed in heterozygotes for recessive alleles to be ...
Evaluation of the Y-Chromosome Structure
Evaluation of the Y-Chromosome Structure

... The MSY1 minisatellite which is the most variable biallelic Y-specific marker contains a 25 AT rich repeat sequence of which between 48 to 114 copies and a minimum of seven base substitution variant repeat sequences (Jobling et al. 1998). The MSY1 is highly polymorphic and an exceptionally high stru ...
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Therapeutic gene modulation

Therapeutic gene modulation refers to the practice of altering the expression of a gene at one of various stages, with a view to alleviate some form of ailment. It differs from gene therapy in that gene modulation seeks to alter the expression of an endogenous gene (perhaps through the introduction of a gene encoding a novel modulatory protein) whereas gene therapy concerns the introduction of a gene whose product aids the recipient directly.Modulation of gene expression can be mediated at the level of transcription by DNA-binding agents (which may be artificial transcription factors), small molecules, or synthetic oligonucleotides. It may also be mediated post-transcriptionally through RNA interference.
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