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.
A red blood cell's function is to transport oxygen.
Answer:
There are many reasons why manned space probes to Saturn are simply unachievable. Getting to space is incredibly hard. The force of gravity is very hard to escape. If you wanted to, you would have to invest trillions upon trillions of dollars to create a space shuttle that may or may not explode. Second, we simply don’t have the technology to make it that far with a manned probe. Saturn is more than a billion miles away. It would take more than several years to go that far. To keep astronauts alive, entertained, and sustained is also a big challenge. In conclusion these are some reasons why a manned space probe to Saturn is unachieveable.
Explanation:
U’d better give me that brainly.
I'm no expert but probably not because eventually they'll get eaten as nature's way of stopping a population get too big (the food chain)
