Answer:
Epigenetic effects can be caused by DNA heterochromatin and/or histone silence or activate.
As such, they can different chromosomes or certain chromosomal regions and be responsible for parental imprinting or influencing gene activity in oxidation and reduction.
Patterns of nucleotide demethylation and hypermethylation are often activate when cancer cells are compared to normal cells.
Explanation:
Cells acquire various patterns of gene expression during differentiation to adapt to a changing environment. Epigenetic and genetic alterations are considered as two independent mechanisms that participate in the onset and progression of cancer. Epigenetic mechanisms can be as important for biological events as genetic mechanisms, which do not imply a change in the DNA sequence, but do have an important role in the modification of gene expression.
Answer:
Carbon Dioxide
Explanation:
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Answer:
In strict mode, the narrow-sense heritability is the proportion of the additive genetic variance that contributes to the total of the phenotypic variance. This value can be associated with the inheritance of the a-thalassemia
.
Explanation:
A-thalassemia is a genetic disorder caused by mutations affecting four different genes that encode alpha-globin, thus affecting the hemoglobin production process and, consequently, oxygen transport. The mode of inheritance of the a-thalassemia may be associated with narrow sense heritability since the phenotype is manifested by gradation, i.e., each allele might contribute in similar mode to this genetic condition.
