Options:
A prostaglandin
B protein hormone
C. peptide hormone
D. steroid hormone
Answer:
Amylin is peptidal harmone. Thus, the correct option is C.
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What is hormone?</h3>
Hormones are the chemical messengers of the body. They make their way through your bloodstream to tissues and organs. They have a long-term effect on a variety of processes, including growth and development.
Amylin is a peptide hormone produced in tandem with insulin by the pancreatic -cell and is hence lacking in diabetics. It works as a satiety agent by inhibiting glucagon secretion and delaying stomach emptying. As a result, amylin replacement could potentially improve glycemic control in some diabetics.
Amylin is a 37-amino-acid peptide hormone released by pancreatic beta-cells in response to a food stimulation together with insulin. It is inadequate in Type 1 diabetes patients and increased in Type 2 diabetes patients in the early stages, a disease marked by hyperinsulinemia.
For more information regarding insulin, visit:
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Answer:
only females
Explanation:
In humans, sex chromosomes in males and females are different. The sex chromosomes found in humans are X and Y chromosomes. X-linked trait is a trait which is inherited on the X- chromosome. According to the question, the trait is passed on a X-linked dominant condition, which means the condition is inherited on the abnormal dominant X-chromosome that will express itself even when in an heterozygous state with a normal X-chromosome.
Hence, a father affected by the condition will have a genotype; XY while a mother that does not have the condition will have a genotype: xx (two normal x chromosomes). Since the Father can only pass his X chromosome to his daughters and never his sons, all his daughters will inherit the condition (see the punnet square in attached image).
N.B: None of the sons will inherit the condition since the mother will pass normal X-chromosomes (x) to her sons.
Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.
All rock on the ocean floor is less than 180 million years old because <span>reverse polarity removed older rock strips magnetized in a different direction. Also,</span> the oldest parts reach the continental crust and then the ocean floor sinks beneath the continental crust, into the mantle.
