The correct answer is A
= 1.3 m/s^2; FN = 63.1 N
-Anonymous
Because it is easily accessible and has a mild immune response, the retina makes a good target for gene therapy.
- In a mouse model, the inner retina was highly effectively transduced by an intravitreally injected adeno-associated virus (AAV) vector.
- The vitreous and internal limiting membrane (ILM) operated as obstacles to transduction in large animals, reducing the efficacy of retinal transduction.
- Before administering AAV vectors, we performed vitrectomy (VIT) and ILM peeling on cynomolgus monkeys to get around these obstacles.
- The findings suggest that surgical ILM peeling prior to AAV vector delivery would be beneficial for retinal disease treatment and safe for effective transduction of the nonhuman primate retina.
Learn more about the adeno-associated virus (AAV) with the help of the given link:
brainly.com/question/28205495
#SPJ4
Grams would be the correct answer hope this helps!
Answer:
In a postsynaptic cell/neuron where a depolarizing change in the membrane potential surpasses the threshold.
Explanation:
Generally, in an excitable cell, the neurotransmitter binding opens the ligand-gated channels at the synapse. Here only the entrance of the ions will not stimulate the action potential. They must exceed the threshold. Hence, an action potential will only get incited when in a postsynaptic cell/neuron, a depolarizing change in the membrane potential surpasses the threshold.
Answer:
the answer is A: solution 1.
Explanation: