Answer:
Bronchioles
Explanation:
You inhale through your nose and the air is filtered. It goes down the pharynx. It goes through the larynx. A "door" called the epiglottis opens during breathing. Then it enters the trachea. (windpipe) It goes through the bronchus. The tertiary bronchi branch into fine tubules called bronchioles, the last passageways for air. Air ends its pathway in the ________. (I bet you can guess because you're so smart!) They're surrounded by capillaries that connect the pulmonary arteries and veins. This enables the transfer of oxygen and carbon dioxide.
I hope this helped!!! Good luck on the test/quiz/project/homework/etc. you're working on! If you want I can give you a l!nk to the article I used. If not, it's fine too. Have a great day!
I think that those are the results of the cross
YYRR : YyRr : yyrr
1 : 2 : 1
25% 50% 25%
<span>In the reaction that builds a fat, hydroxil groups react with carboxyl groups. Both hydroxil and carboxyl are </span><span>functional </span>groups<span> in biological molecules. The h</span>ydroxil group is group of atoms found in organic compounds, expressed with the formula OH. The carboxyl group are found in acids.
It must pass from the nucleus to the ribosomes, hope this helped!
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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