Answer:
An autosomal dominant gene is one that occurs on an autosomal (non-sex determining) chromosome. As it is dominant, the phenotype it gives will be expressed even if the gene is heterozygous.
The chances of an autosomal dominant disorder being inherited are 50% if one parent is heterozygous (NL) for the mutant gene and the other is homozygous for the normal (NN), or 'wild-type', gene. This is because the offspring will always inherit a normal gene from the parent carrying the wild-type genes, and will have a 50% chance of inheriting the mutant gene from the other parent. If the mutant gene is inherited, the offspring will be heterozygous for the mutant gene, and will suffer from the disorder. If the parent with the disorder is homozygous for the gene, the offspring produced from mating with an unaffected parent will always have the disorder.
Explanation:
Please provide an image. But just for reference, a plant cell's main organelles are the cell wall, cell membrane, large water vacuole, nucleus, mitochondria, cloroplast, lysosme, golgi body, and some other organelles that may also be found in animal cells.
<span>Blood is a liquid and has cellular parts. The liquid contains substances such as proteins and lipids. The cellular constituents are erythrocytes (red blood cells), leukocytes and platelets.</span>
Answer:
Cell cycle regulators are the cell cycle only when they are tight bound to CDKS.
Explanation:
To be fully active, the CDK/Cyclin complex must also be phosphorylated in specific locations. Like all kinases, CDKS are enzymes (kinases) that phosphorylate other proteins. Phosphorylation activates the protein by changing its shape.
