Answer:
If a person has a diet high in saturated fats, LDL cholesterol molecules can carry cholesterol from the liver to cells and to the arterial walls whereas HDL cholesterol transports cholesterol from the cells to the liver where it is converted to bile salts which can modulate cardiovascular function.
Explanation:
Cholesterol is a lipid generated in the liver that is used to make hormones and vitamin D, but can also be ingested when eating fats.
Cholesterol can be divided into two types: LDL (low-density lipoprotein) and HDL (high-density lipoprotein).
LDL is commonly known as the "bad cholesterol" and is responsible for the deposit of cholesterol in the walls of arteries, which generates atherosclerosis and can potentially lead to strokes or heart attacks because it occludes the vessels and makes it impossible for the blood to advance.
HDL is also called "good cholesterol" because it takes the cholesterol from the cells to the liver where it'll serve a good cause, instead of blocking the arteries.
To reduce the amount of LDL, it's best to limit the consumption of fatty meats, dairy products and other saturated fats. Foods with a good amount of HDL are those with unsaturated fats, like fish, nuts and seeds.
Answer: mother: XX^aa, father: X^YAa, son: X^YAa, daughter: X^X^aa.
Explanation:
Color blindness is a genetic disorder that affects the ability to distinguish colors. It is hereditary and is transmitted by an X-linked recessive allele. If a male inherits an X chromosome with the altered allele he will be color blind. In contrast, females, who have two X chromosomes, will only be colorblind if both of their X chromosomes have the altered allele. This is because <u>males have one X chromosome and one Y chromosome, while females have two X chromosomes</u>.
If the woman has normal vision, that means she cannot have both chromosomes affected. She can only have one affected chromosome (be a carrier) or none at all. Also, if she has blue eyes, which is a recessive trait, then both alleles are recessive. But the eye color is not on the X chromosome. For example, her eye color genotype can only be aa, because if she had at least one dominant allele she would have brown eye color. As for the other trait, she can be XX^, with X^ being an affected (carrier) allele or XX, i.e. both normal. So in summary, her genotype can be XXaa or XX^aa
If she has a brown-eyed male child who is also colour blind, he has inherited the allele for colour blindness from his mother, since the father does not pass on an X chromosome to the male children, only the Y. With this we can now rule out the mother's XXaa genotype since she had to have passed on her affected X^ chromosome. Then the genotype of the mother is XX^aa. And since her mother can only pass on one allele to (recessive) because she does not have allele A, the dominant that determines her brown eye color can only come from the father. So the genotype of this son is X^YAa. The female daughter has color blindness and blue eyes. So she had to inherit the affected X^ chromosome from the mother (which we already know she has) and an affected X^ chromosome from the father, because the daughter needs to inherit both affected X^ chromosomes to develop the disease. And if she also has blue eyes, she had to have inherited a recessive allele from the mother and another from the father. So with this information we can say that the father's genotype can only be X^YAa. Because the father must have both A and A alleles of the same eye color, because he passed the dominant one to the son and the recessive one to the daughter. At last, the genotype of the daughter is X^X^aa.
Answer:
it would be at the bottom of the hill. That's where all of the energy from the descent is at its peak.
