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.
I think they are called Sutural. Intra sutural bones also known as the wormian bones are extra bone pieces that occur within a suture (a joint) in the cranium. They are irregular isolated bones that appears in addition to the usual centers of ossification of the cranium and they are not rare bone despite being unusual.
Answer:mercury, lead, chromium
Explanation:
The binding of a cell<span> to another </span>cell<span>, or a cell to a </span>surface<span>, via specific </span><span>cell adhesion molecules</span>
<span>Proto-oncogenes are genes that normally help cells grow. When a proto-oncogenemutates (changes) or there are too many copies of it, it becomes a "bad" gene thatcan become permanently turned on or activated when it is not supposed to be. When this happens, the cell grows out of control, which can lead to cancer.....Is this what you need ?</span>
