Answer:
well it would have to be out of your 23 pairs, but which ever it is will have an entire section of the chromosome missing, hence the name deletion.
Explanation:
Answer:
According to the image, the approximate QT interval is 0.4 seconds.
Explanation:
The QT interval is the space between the beginning of the QRS complex and the end of the T wave, which represents from the beginning of depolarization to ventricular repolarization.
Considering that the extandardized measurements of an EKG, where the paper circulates at a speed of 25 mm/s, 1 mm horizontal —measuring time— has an equivalence of 0.04 s.
In the image, there is 10 mm between the beginning of the QRS and the end of the T wave, so:
0.04 seconds X 10 mm = 0.4 seconds.
Then, the estimated QT interval is 0.4 seconds.
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
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Matthias Jacob Schleiden was a German botanist who, with Theodor Schwann, cofounded the cell theory. In 1838 Schleiden defined the cell as the basic unit of plant structure, and a year later Schwann defined the cell as the basic unit of animal structure.
