• 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


... keep at rest in a position comfortable for breathing. Dispose of contents/container in accordance with local/regional/national/international regulations. Thermo Fisher Scientific Baltics UAB , V.A. Graiciuno 8, LT-02241 Vilnius, Lithuania tel. +370 700 55131 ...
High mutation rates in human and ape pseudoautosomal genes
High mutation rates in human and ape pseudoautosomal genes

... (Schiebel et al., 2000). On the other hand, diversity in another human pseudoautosomal gene, SHOX, is not higher than elsewhere in the genome (May et al., 2002). A noncoding pseudoautosomal region close to the Xp/Yp telomere was reported to have a high substitution rate (Cooke et al., 1985; Baird an ...
Identification of eight novel coagulation factor XIII subunit A mutations
Identification of eight novel coagulation factor XIII subunit A mutations

... wild-type residues at the positions of the human FXIIIA mutations. (Refer to Figure 1 for orientation of mutated residue positions with respect to the entire FXIIIA monomer.) (A) Tyr167 shown with hydrogen bonds (thin blue lines) to nearby β-staves (dark green ribbons, arrowheads point in the N-term ...
ppt
ppt

... This protein is a member of the RUNX family of transcription factors and has a Runt DNA-binding domain. It is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can b ...
Premature aging as a consequence of Mis
Premature aging as a consequence of Mis

... protein for composing nuclear lamin, is identified in the HGPS patients (Eriksson, 2003). Werner syndrome (WS), called also “adult progeria”, is a genetic disorder characterized by an early and progressive development of aging features (James, 2005). WS patients are mainly found in Japan. They have ...
Evolutionary dynamics of full genome content in Escherichia coli
Evolutionary dynamics of full genome content in Escherichia coli

... should exist within species where it might be erased by either very high or very low rates of gene transfer and loss. The gene contents of the two closely related and recently derived laboratory isolates, MG1655 and W3110, are very similar, and there is also some degree of correspondence between gen ...
Warren, ST and Nelson, DL: Trinucleotide repeat expansions in neurological disease. Current Opinion in Neurobiology 3:752-759 (1993).
Warren, ST and Nelson, DL: Trinucleotide repeat expansions in neurological disease. Current Opinion in Neurobiology 3:752-759 (1993).

... expanding trinucleotide repeats. However, much remains to be understood, in particular the mechanisms responsible for this unprecedented mutational change. Below are short descriptions of the genetic diseases currently recognized to exhibit these mutations and what is known about each trinucleotide ...
Chado: evolution of a biological database LONG VERSION
Chado: evolution of a biological database LONG VERSION

... Must store representations of genes and genomic entities – Sequence data – Exon-intron structure – Noncoding genes – Curated and computed features – Entities with unusual transcriptional properties ...
papaya X-specific BACs monoica corresponding
papaya X-specific BACs monoica corresponding

... monoecious, having separate male and female flowers on a single individual, with the lack of sexual dimorphism, signifying the absence of sex chromosomes. The genome size of monoica is 626Mb compared to the 372Mb genome of papaya, signifying expansion in monoica since the divergence of these species ...
Proteins
Proteins

... therefore, N- and C-terminus are on neighboring strands of one sheet as in the parent protein H(A16-M). In contrast, cpA16M-84 is produced by opening an interstrand connection, and the new ends are located on different b-sheets. On the gene level the cp variants were generated by separating the codi ...
Divining Biological Pathway Knowledge from High
Divining Biological Pathway Knowledge from High

... The KEGG Node Table now has two extra columns in yellow. ‘Visible Neighbors’ shows the number of genes in each KEGG pathway that are also visible in the Network View. ‘Visible Enrichment’ shows the over-representation statistic for each KEGG pathway calculated using the hypergeometric distribution ...
PDF+Links
PDF+Links

... revealed that carriers of the APOE*4 allele are at a higher risk of the disease than APOE*4 non-carriers. The APP gene encodes a polypeptide of up to 770 amino acids which is probably involved in nuclear signaling (Selkoe, 1998). According to the “amyloid cascade hypothesis”, abnormalities of APP me ...
Familial Hypercholesterolemia
Familial Hypercholesterolemia

...  Patient 3- Homozygous dominant for the LDLR receptor – The most severe form of the disease ...
Strain Review Form
Strain Review Form

... Strain Review for Donating Strains to the CGC (submitting this form does NOT guarantee your strain(s) will be accepted into the collection) Please complete this form and email it to [email protected] BEFORE sending the strains! Strain Name: The lab designation used to name the strain must have been approv ...
Characterization of the metacaspase gene family in Arabidopsis
Characterization of the metacaspase gene family in Arabidopsis

... me with the initial opportunity to work in his lab, an opportunity which helped me to find my direction in life, and for helping to further encourage my future scientific aspirations and career. Victor supported me during the hardest moments of this thesis and I will never forget his kindness. Thank ...
Commonly Asked Questions
Commonly Asked Questions

... spot with signal intensities in both channels below the user defined baseline value (before background subtraction), this spot will be be filtered out (filtering) leaving those features with signal greater than baseline value in at least one channel. A spot whose intensities in only one channel is b ...
reviews
reviews

... The recent results derived from evolutionary, developmental and genomic studies in various organisms highlight the key roles of gene and phenotypic multifunctionality during organismal evolution20,85. Genetic evidence of gene multifunctionality has a long history and was first described in maize86 a ...
Mcbio 316: Exam 2 ANSWER KEY (10) 1. Proteins encoded by the
Mcbio 316: Exam 2 ANSWER KEY (10) 1. Proteins encoded by the

... a. A new Put- mutant was isolated that can revert to Put+ but cannot repair any of these deletions. What can you infer about the type of mutation and where it is located? ANSWER: The new mutant can revert so it is probably NOT a deletion (i.e. it is probably a point mutant). The new mutant cannot re ...
doc
doc

... C) 5.4 10-11 D) The rate of false negatives cannot easily be estimated. 22. What are two of the most commonly used scoring matrices for data bank searches and for aligning protein sequences? A) GTR and Dayhoff Recoding B) PAM and Blosum C) Gonnet and JTT D) none of the above, explain: 23. True/False ...
Overexpression of miR165 Affects Apical
Overexpression of miR165 Affects Apical

... Loss-of-function mutations of the HD-ZIP III genes have been demonstrated to affect various aspects of plant growth and development. It has been shown that loss-of-function mutations of IFL1/REV cause defects in lateral meristem formation, interfascicular fiber differentiation, secondary xylem devel ...
coxL - Université du Québec
coxL - Université du Québec

... CoxL is the large subunit of the CODH. Phylogenetic analysis revealed that coxL gene sequences encompass two main clusters: BMS and OMP but the version conferring a high affinity for CO and the ability to scavenge atmospheric CO is unknown. ...
Overview of molecular methods in immunohematology
Overview of molecular methods in immunohematology

... approach to DNA typing should err on • One-step, automated, objective antibody detection and identification the side of caution. Thus, the strategy • Use of transfected cells as immunogens for production of monoclonal antibodies • Conversion of IgG monoclonal antibodies to IgM direct agglutinins sho ...
Title PPAR interprets a chromatin signature of - DR-NTU
Title PPAR interprets a chromatin signature of - DR-NTU

... synchronously activated [3,5] while some others become repressed [10]. Therefore, it is likely that other factors should be taken into consideration, and in particular the transcription factors that should interpret this epigenetic signature at the time of differentiation. However, if common signal ...
Y Chromosome Markers
Y Chromosome Markers

... Lineage Markers • Great for genealogy or tracing evolution • However, the fact that these markers do not recombine is a disadvantage for Forensics • Cannot use the product rule when determine the probability of an ID match • Cannot separate direct relatives apart: – Y DNA Profile could be any male ...
Hypercholesterolemia
Hypercholesterolemia

... Cholesterol is synthesized in the liver and is absorbed in the intesChemical Structure of Cholesterol. tine from ingested food. It is circulated in body fluids in spherical bodies known as lipoprotein particles. These lipoproteins are classified according to their densities determined by gradient cent ...
< 1 ... 176 177 178 179 180 181 182 183 184 ... 1045 >

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.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report