Answer to Question 1
4
Answer to Question 2
David has a condition called hereditary hemochromatosis that was only discovered in 1996. It is now known that the reason for the increased iron absorption in individuals with hemochromatosis is a defect in the gene (DNA) that codes for one of the transport proteins involved in regulating intestinal iron transport.
Iron is stored intracellularly as ferritin and hemosiderin. Ferritin synthesis is regulated according to iron availability by a system of cytoplasmic binding proteins (IRP-1 and -2) and a noncoding iron regulatory element on mRNA (IRE). When iron is abundant (as in hemochromatosis), sites on the ferritin molecule are blocked from further iron binding, which promotes increased synthesis of ferritin. Ferritin is also the storage form of iron and tends to accumulate in the parenchymal cells in the periportal areas of the liver. With time, and excessive iron absorption, these parenchymal cells of the liver are destroyed and replaced with fibrous tissue, leading to a condition known as hepatic cirrhosis. The destruction of the liver cells from too much iron being deposited releases the liver enzymes, alanine aminotransferase and aspartate aminotransferase. Once the liver enzymes are released, they are detected at high levels in the bloodstream.
Bones of the lower extremity.
Cortical Connections of the Hippocampal Formation
In The Gross Clinic (1875), by Thomas Eakins, Professor Samuel Gross’s team of surgeons cuts through
A charcoal canister can be located under the hood or underneath the vehicle.
Cortical EEG recorded during epileptic attacks. Notice that each trace is characterized by epileptic ...
Bone Formation