Answer:
D) observation that certain tumor-suppressor genes and oncogenes are involved in a sequential manner in the development of colon cancer
Explanation:
Cancer is defined as the abnormal growth of cells of the body. These cells multiply/replicate without control thereby forming a lump or tumor.
Cancer growth has 5 stages and they go though different multi level steps.Different finding backs this up and it includes observation about certain tumor-suppressor genes and oncogenes being involved in a sequential manner in the development of colon cancer.
People with central sleep apnea experience a complete cessation of respiratory activity for brief periods of time yet do not have frequent awakenings and do not tend to feel tired during the day.
<h3>What is sleep apnea?</h3>
Breathing regularly stops and starts during sleep, which is known as sleep apnea. People may have sleep apnea if they snore loudly and still feel exhausted after a full night's sleep.
These are the primary forms of sleep apnea:
The more prevalent type of obstructive sleep apnea happens when throat muscles relax.
Central sleep apnea, which develops when your brain fails to properly activate the breathing muscles,
When a person has both central and obstructive sleep apnea, it is known as complex sleep apnea syndrome, also called treatment-emergent sleep apnea.
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Answer:
Transamination reaction:
Transmaination reaction may be defined as a type of chemical reaction that involves the transfer of an amino group to the another keto acid fort the formation of new amino acid. The non essential amino acid can be easily converted to essential amino acid by this transmination reaction.
This reaction is important for the important mteabolic pathways of the body. The cofactor required for the transamination reaction is pyridoxal-5'-phosphate. This cofactor also works as a derivative of vitamin B6. This cofactor is converted to pyridoxamine-5'-phosphate during the reaction.
Answer:
carries two main function
None of the provided options are reasonable. <span>comparing nutrient concentrations between the photic zone and the benthic zone can not tell you whether differences in concentrations between the photic and benthic zone are due to uptake by phytoplankton or because nutrients are sinking to the sea bottom and ocean stratification is preventing mixing. The approach of c</span><span>ontrasting nutrient uptake by autotrophs at different locations under different temperatures would not provide useful information on limiting nutrients. but rather uptake rates at different temperatures. It is likely that e</span>xperimentally enriching some areas of the ocean and compare their productivity to that of untreated areas can provide an indication of limiting nutrients, but this is not advisable, as it would have to be done on a large scale, and one cannot be sure of the ecological consequences. Also, because it would not be a controlled experiment, other factors could create 'noise' in the data. The last option, <span>observe antarctic ocean productivity from year to year to see if it changes, also does not help, as there is no correlation between nutrient concentrations using this approach. The best approaches would be either the last approach, but with the additional monitoring of nutrient concentrations, or under a controlled laboratory experiment.</span>
