The same causes modify the electrical condition of the atmosphere and the power of the surface to reflect, absorb and radiate the rays of the sun, and consequently influence the distribution of light and heat, and the force and direction of the winds.
Both biological and methodological characteristics were examined in an attempt to explain the possible causes of heterogeneity (i.e., the possible causes modifying the outcome) among the studies.
An increase in the ordering of the solvent molecules leads to a larger solvation force which is repulsive for hydrophilic surfaces and attractive for hydrophobic surfaces causing modified silica particles with hydrophobic surfaces to have better suspension ability during electrolysis, which is a prerequisite for homogeneous co-electrodeposition [13, 34].
Preventing the binding of snRNP U1 (at the donor site) or U2/U5 (at the polypyrimidine moiety and acceptor site) can cause modified splicing, commonly excluding exons from the mature mRNA.
As stated in the plan, "Experience tells us that virtually all human diseases can be caused, modified, or altered by environmental agents.
For example, the identification of disease-associated genetic variations, which are presumed to cause modified immune responses and precede the onset of disease symptoms, could inform stratification of patients into more phenotypically homogeneous subgroups and provide testable hypotheses regarding response to treatment.
It would therefore be expected that there may well be significant variation in disease presentation, diagnostic features and possibly response to therapy according to such differing causes and modified by variables that influence penetrance such as age, sex and ethnicity.
Under the magnetic field, the particles heated up, causing the modified neurons to fire.
The conditions in a proportion of individuals with nonsyndromic hearing loss, particularly in the undiagnosed group, may have been caused or modified by an accumulation of unfavorable variants across multiple genes.
We also use genome editing to explore the mechanisms by which genomic variation causes or modifies disease, for example by introducing disease-associated noncoding SNPs into human cells.
