Biology, 23.12.2019 18:31 MayFlowers
Afamilial form of hypoparathyroidism is caused by a single point mutation in the gene encoding the preproparathyroid hormone. as a consequence of this point mutation, the signal sequence cannot be cleaved from the prepro-form of the mutant hormone. which statement below best describes the effect of this mutation upon synthesis of the preproparathyroid hormone? a) mrna encoding the mutant preproparathyroid hormone would accumulate in the nucleus and not be transcribed. b) the mutant preproparathyroid protein would not be targeted to the endoplasmic reticulum and thus would be translated by free ribosomes in the cytoplasm. c) the mutant preproparathyroid hormone would be incorrectly folded in the endoplasmic reticulum. d) the mutant preproparathyroid hormone would be inserted into the plasma membrane of the parathyroid cells. e) the mutant preproparathyroid hormone could not be stored in secretory vesicles, but instead would be secreted immediately following synthesis.
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Biology, 21.06.2019 23:30
Compare and contrast region e in the illustration above with region d. describe the physical characteristics of each region.
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Biology, 22.06.2019 04:20
When in solution, a molecule that moves slowly across an artificial membrane moves rapidly across a plasma membrane. this molecule rapidly enters the cell regardless of whether its concentration is higher inside or outside the cell. using this information, which transport mechanism is most likely to be responsible for the movement of the molecule across a plasma membrane? view available hint(s)when in solution, a molecule that moves slowly across an artificial membrane moves rapidly across a plasma membrane. this molecule rapidly enters the cell regardless of whether its concentration is higher inside or outside the cell. using this information, which transport mechanism is most likely to be responsible for the movement of the molecule across a plasma membrane? active transportexocytosis
Answers: 2
Afamilial form of hypoparathyroidism is caused by a single point mutation in the gene encoding the p...
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