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. Longer
The shortest wavelength on the left side is Gamma rays. The longest are radio so as you move to the right, it gets longer.
Answer:
Substrate-level phosphorylation, which is a process of forming ATP by the physical addition of a phosphate group to ADP can take place in the cytoplasm during glycolysis or inside the mitochondrial matrix during the Krebs cycle.
Explanation:
Substrate-level phosphorylation is a metabolic reaction that results in the formation of ATP or GTP by the direct transfer of a phosphoryl (PO3) group to ADP or GDP from another phosphorylated compound.
25 x 8
8 x 5 = 40 you put the 4 on top of the 8 and put the zero as your first number on your answer
8 x 2 = 16
then you get the 4 on top of the 8 and then add 16
16 + 8 = 20
20 -- 0
200
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Answer: you test and use your knowledge
Explanation: i got it right
