The answer is that they are somatic cells
<span>If a scientist is trying to determine whether the use of cell phone contributes to brain cancer, then the most significant weakness in this type of study is the relationship between the cell phone and brain cancer itself. It is hard to identify its connections and consequences with each other.</span>
The structure that is labelled C would be a protein, a specific type of protein that helps in regulating the transport of substances in and out of the cell.
Well this has to be your opinion :) but I will tell you autotrophs are organisms that can make their own food, so plants. Heterotrops are organisms that have to get their energy from another source, animals. So would you rather be a plant or animal (like you already are) and why?
Answer:
The correct answer is ''All three are caused by disparate genes, but each gene was found to contain repeats of a unique trinucleotide sequence.''
Explanation:
Four groups of trinucleotide repeats related to DNA expansion have been characterized in the human genome. CGGI GCC, CAGIGTC, CTGIGAC and recently GW CTT sequences. The CGGl GCC sequences are usually located in the noncoding regions of different genes and when expanded they associate with fragile sites on the chromosomes. The CAGIGTC repeats are part of the coding region and are related to different neurodegenerative disorders. You can try to make a classification depending on the unit that is repeated, having on one side a group that are caused by repeats of the CAG trinucleotide (cytosine, adenine, guanine). Huntington's disease (HD) is a progressive disorder of motor, cognitive and psychic function. The disease is inherited in an autosomal dominant manner, and is caused by the expansion of CAG trinucleotide repeats in exon 1 of the gene called huntingtin (HTT or IT-15). Unstable mutations have also been found in which the repeat unit does not is composed of three nucleotides, if not four, such as type 2 myotonic dystrophy, where the tetranucleotide CCTG repeats. Fragile X Syndrome consists of an abnormal expansion of the cytosine-guanine-guanine trinucleotide (CGG) in the FMR1 gene, which prevents intellectual disability and also influences the formation of connective tissue
