Answer:
Sickle cell disease in an autosomal recessive inherited disease which is caused by the mutation in the HBB (hemoglobin-β gene) gene present on the chromosome no. 11. In sickle cell, the red blood cells become sickle shape due to the abnormal shape of hemoglobin present in it.
These sickle cells are known to form a blockage in the blood vessels thereby causing damage to the vital organs. Human spleen constantly destroys sickle cells because they get trapped in it which causes a disease called sickle cell anemia.
Sickle cell anemia is normally the problem in genetic disease which is inherited from the parents to children. When both the DNA strand has a mutation in their HBB gene then only this disease will affect the individual.
Answer:
thymine(t)
cytosine(c)
56
44
35
Explanation:
A always pairs with T, so 56 A's will pair with <u>56</u> T's
G always pairs with C, so 44 G's will pair with <u>44</u> C's
100 base pairs means there are 200 bases present altogether
out of 200, we have 65 T's so ultimately we will have 65 A's
we are now left with 70, of which have will be C and half G, which gives 35 C's and G's
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Vitamins help them function as fats.
Answer :<em> That trough time, a specie of animal, plant, bacteria can change.
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<em>When a life form reproduces, one of its"babies" may be different from its parents because of genetic mutation. </em>
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Answer:
Glucose: is a simple sugar which is an important energy source in living organisms and is a component of many carbohydrates.
Fructose: or fruit sugar, is a simple ketonic monosaccharide found in many plants.
Deoxyribose: sugar derived from ribose by replacing a hydroxyl group with hydrogen.
Ribose: is a kind of sugar that is produced by the body. It is used as a medicine. Ribose is used for heart disease, mental function, athletic performance, chronic fatigue syndrome (CFS), fibromyalgia, and many other conditions, but there is no good scientific evidence to support these uses.
Glyceraldehyde (glyceral) is a triose monosaccharide with chemical formula
Explanation: