Answer:
D. Hydrolysis
Explanation:
Dehydration synthesis reactions build molecules up and generally require energy, while hydrolysis reactions break molecules down and generally release energy. Carbohydrates, proteins, and nucleic acids are built up and broken down via these types of reactions, although the monomers involved are different in each case.
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This question isn't really finished, but bacterium are unicellular prokaryote.
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The moon has less gravity because it is smaller than the Earth.
Answer:
The three-chambered hearts of amphibians and nonbird reptiles are facultative, allowing variation in blood flow through the heart.
Explanation:
In Anatomy, cardiac cycle can be defined as a complete heartbeat of the human heart which comprises of sequential alternating contraction and relaxation of the atria and ventricles, therefore causing blood to flow unidirectionally (one direction) throughout the human body.
Generally, the cardiac cycle occurs in two (2) stages;
I. Diastole : in this stage, the ventricles is relaxed and would be filled with blood.
II. Systole: at this stage, the muscles contracts and thus, allow blood to be pushed through the atria.
All amphibians and reptiles except for crocodiles (having four-chambered heart) have three-chambered hearts, which typically comprises of a partially divided ventricle and two atria.
Hence, the correct statement about the three-chambered hearts of amphibians and nonbird reptiles is that, the three-chambered hearts of amphibians and nonbird reptiles are facultative, allowing variation in blood flow through the heart due to the partially divided ventricle.
<h2>CRISPR/Cas9</h2>
Explanation:
CRISPR can be used to reintroduce dystrophin back into the KO mouse
- CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats and is used to for gene editing
- CRISPR/Cas-mediated genome editing has been shown to permanently correct DMD mutations and restore dystrophin function in mouse models
- Germline editing by injecting zygotes with CRISPR/Cas9 editing component was first done in mdx mice by correcting the mutated exon 23
- Postnatal editing of mdx mice was then achieved using recombinant adeno-associated virus to deliver CRISPR/Cas9 genome editing components and correct the dystrophin gene by skipping or deleting the mutated exon 23 in vivo
- Germline and postnatal CRISPR/Cas9 editing approaches both successfully restored dystrophin function in the mice and same technique can be used for KO mouse model
