stimulants. There's also a Quizlet that has this exact question if you would like a link.
Answer:
Explanation:
NADH and FADH2 are both electron carriers of the electron transport chain. NADH gives up its electrons starting from Complex I, which has a higher energy level compared to other complexes. Energy is given off to pump protons across the membrane by the time electrons are transferred to ComplexIII. More electrons are pumped across the membrane as electrons move to Complex IV. Because NADH commenced giving up its electrons from Complex I (higher energy level complex), more protons are pumped across the membrane gradient, which enables ATP synthase with more power to produce 3ATP molecules per NADH molecule.
On the other hand, 2 molecules of ATP are generated by FADH2 because it starts by giving up its electrons to ComplexII. It missed a chance to pump protons across the membrane when it passed Complex I. By the time the electrons reach Complex IV, less protons have been pumped. The lesser the protons to power ATP synthase, the lesser the ATP molecules produced.
Answer:
The claim by the researcher is supported because of the known functions of insulin and growth factors. Both hormones have a tendency to respond to the presence of glucose. The growth hormone initiates STAT5 signaling for producing the Igf-1 factor that is important for utilizing glucose. The insulin hormone is well known for utilizing glucose.
Pelvic inflammatory diseases (PID)
<span>Pelvic inflammatory
diseases (PID) is an diseases that affect 10-40% of women who had an infection
of either gonorrhea or chlamydia and it usually occur when the initial
infection such as chlamydia or gonorrhea
travels upward with other bacterias beyond the the cervix into the uterus,ovaries,
oviducts and pelvic cavity. However, PID is major cause of infertility in young
women.</span>
Answer:
a. Trisomic
Explanation:
A trisomy is a genomic phenomenon whereby a particular chromosome is present in three copies. In this case, the trisomy involves the chromosome P, being this species a tetraploid with 5 pairs of homologous chromosomes (2n = 10). In humans, the trisomy for chromosome 21 is one of the most common types of aneuploidies that lead to the Down syndrome by producing alterations in gene expression patterns that are associated with changes in the phenotype
