<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
The nucleus contains most of the genetic material, or DNA, of the cell.
Answer:
The correct answer is option B ( ligand gated channels opened by neurotransmitter molecules).
Explanation:
Input region or postsynaptic region or dendrite is the site of neuron cell which receives the impulse from the pre-synaptic neuron at the synaptic junction.
The cell membrane of the dendrite is embedded with ligand-gated channels which opens up in response to the ligand (neurotransmitters) produced by the neurotransmitter vesicle of axon or output region of neuron.
The neuromuscular junction is such a case where acetylcholine receptors present in the dendrite opens in the presence of acetylcholine.
Thus, option B ( ligand-gated channels opened by neurotransmitter molecules) is the correct option.
Answer:
Chemical. quimico
Explanation:
Hope this helps. Chemical, because it's being exposed, no one is exposing it.
Espero que esto ayude. Quimico, porque esta expuesto, nadie lo esta exponiendo.
se un poco de espanol
buena suerte
