Changes in the shape of a cell usually involve a reorganization of the
cytoskeleton.
Cytoskeleton is an interwind filamentous network that mainly keeps and mantains the shape as well as internal organization.
- Hence reorganization is also done with the help of the cytoskeleton.
- Extracellular matrix mainly helps the cell to keep it together.
- Transporter proteins mainly act as a catalyzing agent for various purposes.
- Nucleus is just a genetic material carrying an organelle that regulates the activities of cells.
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<span>A pedal steel guitar uses foot pedals and knee levers. It </span>allows the player to change pitches with his feet and knees (apex). <span>A pedal (or foot pedal) is something you can use if you want to alter the sound coming from your guitar or add various sound effects.</span>
If the live enzyme fructose 1,6- bisphosphatase defect is occured and this results in an abnormally high levels of lactate in the blood plasme this will result into the lactate will accumulate into the blood.
What is the work of fructose 1,6-biphosphatase enzyme?
In the liver, gluconeogenesis converts lactate to glucose. If FBPase-1 is defective, lactate cannot enter the gluconeogenic pathway in hepatocytes, building up in the blood.
A crucial enzyme in gluconeogenesis is fructose 1,6-bisphosphatase (FBPase). It is a possible target for drugs used to treat type II diabetes. Additionally, the protein is linked to a rare genetic metabolic disorder, and certain cancer cells lack the activity of the enzyme FBPase, which encourages glycolysis and aids in the Warburg effect.
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Answer:
Graham had more power than Marshall
For an individual to have the behavioral expression of the disorder pku, the individual must inherit a recessive combination of alleles and be exposed to phenylalanine in the diet.
What is pku?
A rare genetic condition known as phenylketonuria, or PKU, causes the body to accumulate phenylalanine, an amino acid. The phenylalanine hydroxylase (PAH) gene is altered in PKU. The enzyme required to degrade phenylalanine is produced in part because to this gene.
When a person with PKU consumes protein-containing foods or aspartame, an artificial sweetener, a dangerous buildup of phenylalanine can occur because this person lacks the enzyme required to break down phenylalanine. This may ultimately result in severe health issues.
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