During a limited movement of the nerve, axonal transport also <u>slows down</u>.
Axonal transport/axoplasmic transport/axoplasmic flow, is a cellular process responsible for movement of mitochondria, lipids, synaptic vesicles, proteins, and other organelles to and from a neuron's cell body, through the cytoplasm of its axon called the axoplasm.
Slow axonal transport is the movement of cytoskeletal polymers and cytosolic protein complexes along axons at average rates on the order of millimeters per day, which corresponds to nanometers per second.
Axon transport mechanisms play a major role in transporting nutrients, organelles and other molecules towards the presynaptic terminals.
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1.The trait is recessive. This means both your parents were carries, but did not show the trait. For example, B represents the allele, you're parents would have to both be Bb. This means that they are carriers, and you could have inherited either BB/Bb/bb - you actually inherited bb, which means because its a recessive trait you will show the trait.
2. For your children, it depends on who you have them with. Because you're bb, you will definitely pass on the b allele, so any child you have would be a carrier and could potentially have the trait. If you have a child with someone BB, all your offspring will be Bb (carriers- as the kid gets one allele form each parent). If you have a child with someone who is bb, all your kids would definitely have the trait. However, if you have a child with someone who as Bb, then the four outcomes are Bb Bb bb bb, so there would be a 50% chance of your kid having the trait.
Hope this helps!! :)
Answer:
The correct answer is d.
Explanation:
Hydranencephaly is a rare congenital anomaly characterized by the absence and replacement of the cerebral hemispheres by cerebrospinal fluid and necrotic remains, with preservation of the membranes (leptomeninges), within a skull of normal capacity and shape. It is the most severe form of cortical destruction cerebral bilateral and is considered an extreme form of porencephaly (focal cystic cavity). It mainly affects the territory of the internal carotid artery and middle cerebral artery, with preservation of the territories supplied by the vertebrobasilar arteries. The most accepted etiology is carotid vascular insufficiency, due to multiple causes (bleeding, placental thromboembolism, arteritis, vascular malformations, among others).
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