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.
Answer:
Hypothesis, controlled conditions, "if then" statement, scientific investigation, observation.
Explanation:
Hypothesis: An idea proposed for an argument to be tested if it's true.
Controlled Conditions: An experiment that doesn't manipulate the independent variable.
If then statements: These sentences present situations and their outcomes.
Scientific Investigation: A plan for asking questions and testing possible answers.
Observation: Using one of the senses (hearing, seeing, tasting, smell, touching) or measurements to gather data.
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This is probably to increase blood supply in the intestines. Blood is a transporter of digested food materials.
Through the roots which soak up the water from surrounding soil
