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.
<span>Any type of pharmaceutical product or dietary supplement must be tested in clinical trials before they can be marketed in order to assess their safety for the general public's consumption and to confirm their intended purpose. While not a complete fail safe, these tests intend to prove a reasonable sense of safety for the product.</span>
Answer:
<em>In the lungs, the blood receives oxygen then leaves through the pulmonary veins. It returns to the heart and enters the left </em><em>atrium</em><em>.</em>
Answer:
the all type of algae are included in kingdom plantae
