I think there’s some data missing! Is it possible to have the graphs with the reaction rate please?
Answer: The answer is Calcium.
Explanation:
Duchenne muscular dystrophy is an X-linked recessive inheritance disorder that is passed from the mother (the carrier) to the child, mostly the male. It is a disorder of progressive muscular weakness. Those who inherit it have a defective gene related to dystrophin which is a muscular protein. The gene that makes Dystrophin is broken and the muscles become weak. Calcium molecules also build up in the muscles.
This causes muscle weakness, frequent falls, trouble running or climbing the stairs and dependency on wheel chairs.
Answer:
The cosmic microwave background radiation.
This is completely consistent with a fireball event in which the radiation field was in thermal equilibrium, and is perhaps the most convincing evidence for the Big Bang.
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Answer:
option #3
Explanation:
each tropic level gets only 10% of the energy from the thing it eats because that organism uses loses energy when it moves or by heat.
Solution:
Fetal programming occurs during embryonic and fetal development, a critical period in which tissues and organs are created. Insufficient nutrition during this time results in permanent alterations to certain structural and physiological metabolic functions of the fetus. British epidemiologist Barker first established the hypothesis, known as the "Barker hypothesis,” which states such programmed changes during this critical period predispose the fetus to certain postnatal diseases. The critical period coincides with the timing of rapid cell differentiation. Essentially, it refers to the process of sustaining or affecting a stimulus or impairment that occurs at a crucial point in its development.
Rickets has long demonstrated that under nutrition in the critical early stages of life brings about a continuing change in structure. A recent new doctrine suggests that fetal programming can affect diseases in adulthood. That is, the body's “memory” of under nutrition during the early stages of development translates into a pathology that determines future diseases. This idea is based on animal studies that demonstrate how under nutrition in utero can alter blood pressure, cholesterol metabolism, insulin response to glucose, and other metabolic, endocrine, and immune functions important to human diseases. This paper reviews evidence of the correlation between fetal under nutrition and diseases found in previous studies and considers the mechanism of fetal programming and the role of the placenta.