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L-Lysin-Production with Corynebacterium glutamicum
L-Lysin-Production with Corynebacterium glutamicum

... shown in green (amplification) and red (attenuation),projecting the flux changes required for the predicted flux scenario for optimum production.This comprised the experimental quantification of the in vivofluxes in the wildtype Corynebacterium glutamicum ATCC 13032(a)andintherationallydesignedlysin ...
ADOPS - Automatic Detection Of Positively Selected Sites 1
ADOPS - Automatic Detection Of Positively Selected Sites 1

... brucei genes [17], at the vertebrate skeletal muscle sodium channel gene [18], at the p53 gene [19], the fruitless gene in Anastrepha fruit flies [20], CC chemokine receptor proteins [21], or at the plant genes that are involved in gametophytic self-incompatibility specificity determination [22, 23, ...
Chapter 22 MOLECULAR AND CLINICAL GENETICS OF RYR1
Chapter 22 MOLECULAR AND CLINICAL GENETICS OF RYR1

... mutations in the RYR1 gene. The mutations appear to cluster in three main regions of the RYR1 gene: an N-terminal region ranging from amino acid residues 35 to 614, a mid region from residues 2060 to 2458 and a Cterminal region from residues 4214 to 4940 with the latter region being predominantly as ...
Artemis Reference
Artemis Reference

... genomes with their associated features. The middle window shows red blocks, which span this middle layer and link conserved regions within the two genomes, above and below. Consequently, if you were comparing two identical genome sequences you would see a solid red block extending over the length of ...
Understanding Lynch Syndrome - Hereditary Nonpolyposis
Understanding Lynch Syndrome - Hereditary Nonpolyposis

... tumour tissue from a person who has had colorectal cancer. Your genetic counsellor can help to get a stored tumour sample from the hospital where the cancer surgery was done. Two different tests can be performed on the tumour sample to see whether a Lynch syndrome gene mutation is likely to be found ...
A novel mutation in the short-wavelength-sensitive
A novel mutation in the short-wavelength-sensitive

... administrations of Lanthony’s Desaturated D15 test, with the cap order 1, 2, 3, 5, 4, 6, 7, 15, 14, 13, 12, 11, 8, 9, 10. On the Farnsworth Panel D15 test, his performance was perfect on the first administration, but he reversed the first two caps upon retesting. Taken together, subject 4041’s perfo ...
Base Composition and Translational Selection are Insufficient to
Base Composition and Translational Selection are Insufficient to

... Geminiviridae contain a comparable number of species with at least 15 sequences available for analysis (22 and 24, respectively). There were fewer appropriate Luteoviridae for analysis (8), but similar to the Geminiviridae, monocot- and dicot- infecting luteoviruses are organized into separate gener ...
Evidence for Mito-Nuclear and Sex-Linked Reproductive Barriers
Evidence for Mito-Nuclear and Sex-Linked Reproductive Barriers

... populations on mainland Italy and Spanish sparrow populations on Sardinia. Early generation migrants were present in both locations indicating ongoing gene flow through dispersal events (Figure 1). As gene flow was observed between the Italian sparrow and both parent species, we implemented a cline ...
Genetics of Colorectal Cancer - Scioto County Medical Society
Genetics of Colorectal Cancer - Scioto County Medical Society

... If diagnoses are correct: Ted has no family history indicative of a known colon cancer syndrome (HNPCC, FAP, other) ...
full text pdf
full text pdf

... (OP) have a benign self-limited disease in which pathologic changes are restricted to the oral mucosa. On the other hand, patients with ocular cicatricial pemphigoid, a chronic condition marked by relapses and remissions, have ocular involvement and also perhaps involvement of other mucous membranes ...
A phenotype-based screen for embryonic lethal mutations in the mouse
A phenotype-based screen for embryonic lethal mutations in the mouse

... is similar to that produced by the spontaneous mutation open brain (opb) (17). The mutation responsible for the 118 phenotype maps to the same 3.2-cM interval as does opb (ref. 18; Table 1). We crossed 118 and opb heterozygous animals and found that the two mutations failed to complement (Fig. 2F); ...
Course Outline
Course Outline

... are only about 80 nm. Most viruses are unable to be seen with a light microscope so scanning and transmission electron microscopes are used to visualise virus particles. To increase the contrast between viruses and the background, electron-dense "stains" are used. These are solutions of salts of he ...
Evolutionary aspects of recombination in RNA viruses
Evolutionary aspects of recombination in RNA viruses

... classified as ‘ homologous recombination ’ (Lai, 1992) since it involves not just homologous parental RNAs, but also crossovers at homologous sites. However, this is not always the case ; hybrid sequences resulting from aberrant homologous recombination (when similar viruses exchange sequence withou ...
Early germline development in Caenorhabditis elegans
Early germline development in Caenorhabditis elegans

... however, is not the only transcription factor whose activity is inhibited by PIE-1, since skn-1;pie-1 double mutants still make no primordial germ cells (Mello et al., 1992) and since PIE-1 inhibits the expression of transcripts that do not depend on SKN-1 for expression (Seydoux et al., 1996). Thes ...
shRNA FAQ - Functional Genomics Facility
shRNA FAQ - Functional Genomics Facility

Obtaining genetic testing in pediatric epilepsy
Obtaining genetic testing in pediatric epilepsy

... X-linked infantile spasms (CDKL5 and ARX) Mutations in CDKL5 are inherited in an X-linked dominant fashion and are a common cause of infantile spasms (IS) and early onset seizures. CDKL5 is responsible for 8% of early onset seizures (<9 months) in girls and 28% of early onset seizures with infantile ...
Stage-specific expressions of four different ribonuclease H genes in
Stage-specific expressions of four different ribonuclease H genes in

... have many similarities in metabolic pathways and vital molecular structures with humans, they harbor many unique biochemical features that can be exploited for the development of rational chemotherapy against these human pathogens. The diseases caused by these pests are incurable in the chronic stag ...
Series 1: Cross Diagrams There are two alleles for each trait in a
Series 1: Cross Diagrams There are two alleles for each trait in a

... There are two alleles for each trait in a diploid organism In C. elegans gene symbols are ALWAYS italicized. To represent two different genes on the same chromosome: When both genes are wild-type: + is the wild type or non-mutant form of a gene: ...
Leveraging SADI Semantic Web Services to Exploit Fish Ecotoxicology Data
Leveraging SADI Semantic Web Services to Exploit Fish Ecotoxicology Data

... knowledge domains provide the subject for the example queries, described in the results. An important requirement for the analysis of a fish toxicological dataset is the ability to compare experimental results with existing published data. This has the potential to provide valuable insights into tra ...
Mendel`s Principle of Independent Assortment
Mendel`s Principle of Independent Assortment

... both deafness and albinism. ...
View PDF
View PDF

... and p2 lie outside the repeat, one within the repeat, which is added in limiting amounts (0.1 pmol/L) that also has a sequence-tail complementary to the fourth universal primer (1 pmol/L). Reaction one included p1 and p2 and reaction two included p1, p3R and p4CTG. Each reaction was performed in a 2 ...
The Familial Pancreatic Cancer Family Registry -
The Familial Pancreatic Cancer Family Registry -

... with allergies were less likely to develop pancreatic cancer. This was especially true for people who reported having hay fever. People who said they were allergic to animals (such as cats, horses, and birds) were also less likely to develop pancreatic cancer. The study also looked at how two genes ...
Tumor Suppressor Genes
Tumor Suppressor Genes

... lives with far more chromosomes than they really need to grow and survive. Sometimes, the chromosomes from one parent are preferentially shed. For example, when human and mouse cells are fused, the descendant hybrid cells shed human chromosomes progressively until only a small minority of chromosome ...
THE LOCI OF EVOLUTION: HOW PREDICTABLE IS GENETIC
THE LOCI OF EVOLUTION: HOW PREDICTABLE IS GENETIC

... The coding region is the part of a gene that encodes the final gene product, either a protein or a mature RNA (Fig. 1). One can distinguish three main types of mutations: (1) coding changes, which alter the amino-acid sequence or the mature RNA nucleotide sequence; (2) cis-regulatory changes, which ...
the loci of evolution: how predictable is genetic
the loci of evolution: how predictable is genetic

... The coding region is the part of a gene that encodes the final gene product, either a protein or a mature RNA (Fig. 1). One can distinguish three main types of mutations: (1) coding changes, which alter the amino-acid sequence or the mature RNA nucleotide sequence; (2) cis-regulatory changes, which ...
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RNA-Seq



RNA-seq (RNA sequencing), also called whole transcriptome shotgun sequencing (WTSS), is a technology that uses the capabilities of next-generation sequencing to reveal a snapshot of RNA presence and quantity from a genome at a given moment in time.
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