I would say C because our body is continuously changing through puberty. We need more sleep, more food consumption, we need to have fantastic hygiene, etc...
Some fossil snakes have remnants of hip bones and legs even though these animals had no legs. These remnant structures are best described as:<u> vestigial structures</u>.
Vestigial structures are organic structures that do not appear to fulfill any important biological function in the organism that possesses them.
- These structures are preserved as an inheritance of the evolutionary process, because at some point in the history of evolution an ancestor of the current species had that structure.
- These types of structures, which can be bones, organs, structures in the skin or any other part of the body, no longer offer any meaningful function for the body.
- The presence of vestigial structures in animals is considered proof that evolution and natural selection exists.
Therefore, we can conclude that some fossil snakes have remnants of hip bones and legs even though these animals had no legs. These remnant structures are best described as vestigial structures.
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Answer:
Its Located in the Plant Cell called Vacuole
Answer:
It controls opening and closing movements of the stomata, but that isn't one of the answer choices.
Explanation:
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.
