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they also form rocks in earth surface
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The type of mutation that causes this translation error is called deletion. Deletion occurs when a section of a DNA is deleted or lost. In cystic fibrosis, three nucleotides are deleted that results in the lost of phenylalanine
Maybe Ashema. If that, it won’t be too hectic I’m sure maybe issues with ashema while he’s young and may fade early it depends.
I'm pretty sure it's primary growth. I might not have studied this type of biology yet, but secondary growth would definitely not be the answer.<span />
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Vasopressin or antidiuretic hormone (ADH) or arginine vasopressin (AVP) is a nonapeptide synthesized in the hypothalamus. Science has known it to play essential roles in the control of the body’s osmotic balance, blood pressure regulation, sodium homeostasis, and kidney functioning. Given its vital role in multiple functions, it is no surprise that ADH is of great clinical significance. ADH primarily affects the ability of the kidney to reabsorb water; when present, ADH induces expression of water transport proteins in the late distal tubule and collecting duct to increase water reabsorption. Several disease states arise when the body loses control of ADH secretion or responds to its presence.
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