Answer:
Human papilloma virus.
Explanation:
STDs are sexually transmitted disease that are more often transferred through the sexual contact. They are the common contagious disease that affects the human population.
Genital warts are marked by the pink or brown swellings near the genital area. They can occur on any reproductive part of the body. The causative agent of the warts is the human papilloma virus and can be converted into cancer if left untreated.
Thus, the answer is human papilloma virus.
Answer:
C. active transport driven directly or indirectly by metabolic energy
Explanation:
The intestinal mucosa is the tissue that lines the inner walls of the intestines. It is characterized by the pleated appearance, which facilitates the absorption of nutrients already deferred and the formation of fecal cake. Most nutrients are absorbed by this region through active transport directly or indirectly driven by metabolic energy.
Answer:
Almost all of the cells in your body share the same DNA as was found in that first cell. Eyes and heart are so different because different set of problems are made in the various eyes and heart cell
Explanation:
a
Cell wall won’t be found in a animal cell since it’s only there in a plant cell.
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.
