Answer:
The answer for writing 421,700 km in scientific notation is A
D- Biosphere
The part of the earth and its atmosphere in which living organisms exist or that is capable of supporting life
No need for evacuation but continue groundwater monitoring due to lower dose of toxic substance.
No need for evacuation, continue groundwater monitoring because the dose of toxic substance in a normal or safe range. In this range the toxic substance can't affect the health of people who drink that water.
If the dose of toxic substance increases more than 10 mg/ kg then the toxic substance killed people who drink that water. According to the graph, we can see that the dose is in a normal range so we can conclude that no need of evacuation for the people.
Learn more: brainly.com/question/24926735
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