Answer:
In order below the answers:
Homozygous males
heterozygous females
curly wings
dark bodies
curly wings and dark bodies
homozygous recessive
heterozygous
straight winged flies
This statement is true.
<span>Agonal gasps are not normal breathing and may be present in the first minutes after sudden cardiac arrest.
It can sound like a snore with somehow long intervals between one gasp and another as it usually occurs at slow rates.</span>
Answer:
Phenotype is physical appearance of the individual while genotype is the genetic makeup of the individual.
Explanation:
Two parents having normal phenotype but effected individual is due to the parents may be Carrier for the particular deseis and the gene responsible for the desies may be in recessive form and the parents are not effected. The gene is not present in dominant form and can not show its effect but the parents are not effected and the daughter may be affected by certain desiese.
The axon terminals of neurons of the hypothalamic-hypophyseal tracts store and secrete ADH and oxytocin in the capillaries of the inferior hypophyseal artery.
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Hypophyseal artery:</h3>
The infundibulum of the pituitary gland, the pars tuberalis, and the median eminence are all supplied by the superior hypophyseal artery. It is a branch of the internal carotid artery's cerebral portion. In order to supply the hypothalamus, the superior hypophyseal arteries split off from the internal carotid arteries, forming a capillary network in the median eminence that is not protected by the blood-brain barrier. The infundibular plexuses and the stalk, respectively, are the sources of the long and short hypophyseal portal veins.
The C6 section of the internal carotid artery gives rise to the superior hypophyseal artery (or arteries). Within 5 mm of the ocular artery's origin, it often arises as a single trunk from the internal carotid artery's medial or posteromedial side.
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Answer:
D. acetyl CoA, NADH, H+, and CO2.
Explanation:
Pyruvate formed by the glycolytic breakdown of glucose enters Kreb's cycle in the form of acetyl CoA. Conversion of pyruvate into acetyl CoA occurs in the mitochondrial matrix and the reaction catalyzed by the pyruvate dehydrogenase complex (PDH). It is an oxidative decarboxylation of pyruvate.
The PDH complex is composed of multiple copies of three enzymes. The enzyme complex catalyzes an irreversible oxidation process in which the carboxyl group of pyruvate is removed as a molecule of CO2 and the two remaining carbons become the acetyl group of acetyl-CoA. Here, NAD+ serves as the electron acceptor and is converted into NADH.
