Answer:
Yes, the model of the helium atom is showing an ion.
Explanation:
Helium, with an atomic number of 2, should have 2 protons and 2 electrons; however, the model only depicts 1 electron. That means the helium must have lost an electron, making it a +1 charge and an ion.
Hi! The answer is fulguration.
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Payshence xoxo
Answer: The hepatic portal vein is one of the most important vein that receives blood from the body and transports it into the liver for filtration and processing. This vein is part of the hepatic portal system that receives all of the blood draining from the abdominal digestive tract, as well as from the pancreas, gallbladder, and spleen.
‘Hepatic’ means of or relating to the liver, therefore the hepatic portal vein is a blood vessel that sends nutrient-rich blood from the gastrointestinal tract and spleen to the liver, but also delivers toxins to the liver that will be chemically modified in the proces of detoxication
A population that has been isolated, especially a smaller one, could have a high level of homozygosity and therefore not a lot of genetic variation. Gene flow between such populations can increase the level of heterozygosity, and therefore up genetic variation.
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.