Answer:
Hypoplasia
Explanation:
Congenital hypothyroidism is most often the result of hypoplasia. Hypoplasia is the process of incomplete development of an organ or tissue in the body. Congenital hypothyroidism is insufficient thyroid hormone production in newborn infants. The underdevelopment of thyroid gland, occurs when the fetus is still in the womb and can be seen in everywhere from tooth enamel to the corpus callosum of the brain, heart, ovaries, various muscle groups, and other regions.
Congenital hypothyroidism is most often the result of thyroid dysgenesis or underdevelopment of the hypothyroid gland.
Congenital hypothyroidism can occasionally also be brought on by a problem with how thyroid hormone is made or by a lack of iodine during fetal development.
Genetic changes or other factors that obstruct normal thyroid gland development can lead to thyroid dysgenesis. TSH receptor gene, PAX8 gene, and NKX2-1 gene mutations are a few genetic changes linked to congenital hypothyroidism.
Mothers who do not get enough iodine, pregnant women who are exposed to radiation, and people who are exposed to certain drugs or chemicals are other causes that may cause thyroid dysgenesis.
Learn more about Congenital hypothyroidism
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The answer is enzymes. Enzymes are biological catalysts and increase the speed of change from substrate to product. The name of enzymes is usually derived from the substrate they break down. For example, lactase breaks down sugar lactose. The name of enzymes contains suffix -ase, for instance, carbonic anhydrase, lactase, lipase, amylase, etc.
co-adaptation
mass extinction
instantaneous speciation
A particular plant species is pollinated by a certain insect species. The insect species depends on the plant species for food. This relationship is based on co-adaptation.
Here co-adaptation refers to the mutual adaptation between the given species(plants and insects) that depend upon each other.
The pathway that uses fat reserves to produce ATP is called lipolysis. It involves the breakdown of triglycerides into fatty acids and glycerol, which are then processed to generate ATP.
The pathway that uses fat reserves to produce ATP is called lipolysis. During lipolysis, triglycerides are broken down into fatty acids and glycerol. The fatty acids are then oxidized through a process called β-oxidation to produce acetyl CoA, which enters the Krebs cycle to generate ATP.
This pathway is used when glucose levels are low and provides a significant amount of energy for the human body. Thus, Lipolysis is the biological process by which triglycerides (fats) are broken down into glycerol and fatty acids, releasing stored energy for cellular use, particularly during periods of energy demand.
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B. A ribose sugar
C. A phosphate molecule
Hewwoo :3
What molecule must be removed in order to rebuild ADP into ATP?
In order to answer your question, you must look at the chemical structures of ADP and ATP. ATP has an adenine that goes by 9' nitrogen to 1' carbon (ribose sugar). In turn, the 5' carbon is attached to a triphosphate molecule. You can see that there's no such thing as a water molecule there. Thus, a water molecule was presumably removed during chemiosmotic phosphorylation.
Answer: A. a water molecule