Answer:
This voice box occurs in all amphibians but is anatomically most complex in frogs. The larynx exits into the trachea; the latter bifurcates into the bronchi and then into the lungs. The glottis then opens, and elastic recoil of the lungs forces the pulmonary air out and over the new air in the buccopharyngeal pocket.
Explanation:
Answer:
9:3:3:1
Explanation:
A dihybrid cross tracks two traits. Both parents are heterozygous, and one allele for each trait exhibits complete dominance *. This means that both parents have recessive alleles, but exhibit the dominant phenotype. The phenotype ratio predicted for dihybrid cross is 9:3:3:1. (There's a calculator on google that show the outcomes just to let ya know) hope it's correct .
The correct order in the blanks are as follows: <u>C A E F G B</u>
c. glucose is actively transported in to the phloem
a. Water enters the phloem through osmosis
e. Pressure from the leaves pushes the water and glucose through the phloem
f. An area of low glucose concentration is reached
g. Glucose is actively transported out of the phloem
b. Water exits the phloem through osmosis
<h3>
What is translocation?</h3>
The transport of sugar created during photosynthesis to all other areas of the plant for respiration and the other activities mentioned above is known as translocation.
Utilizing light energy, plants use photosynthesis to convert the inorganic chemicals carbon dioxide and water into glucose. Respiration uses a portion of the glucose created by photosynthesis. The seven biological processes receive energy as a result.
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Answer:
One of the common genetic disorders is sickle cell anemia, in which 2 recessive alleles must meet to allow for destruction and alteration in the morphology of red blood cells. This usually leads to loss of proper binding of oxygen to hemoglobin and curved, sickle-shaped erythrocytes. The mutation causing this disease occurs in the 6th codon of the HBB gene encoding the hemoglobin subunit β (β-globin), a protein, serving as an integral part of the adult hemoglobin A (HbA), which is a heterotetramer of 2 α chains and 2 β chains that is responsible for binding to the oxygen in the blood. This mutation changes a charged glutamic acid to a hydrophobic valine residue and disrupts the tertiary structure and stability of the hemoglobin molecule. Since in the field of protein intrinsic disorder, charged and polar residues are typically considered as disorder promoting, in opposite to the order-promoting non-polar hydrophobic residues, in this study we attempted to answer a question if intrinsic disorder might have a role in the pathogenesis of sickle cell anemia. To this end, several disorder predictors were utilized to evaluate the presence of intrinsically disordered regions in all subunits of human hemoglobin: α, β, δ, ε, ζ, γ1, and γ2. Then, structural analysis was completed by using the SWISS-MODEL Repository to visualize the outputs of the disorder predictors. Finally, Uniprot STRING and D2P2 were used to determine biochemical interactome and protein partners for each hemoglobin subunit along with analyzing their posttranslational modifications. All these properties were used to determine any differences between the 6 different types of subunits of hemoglobin and to correlate the mutation leading to sickle cell anemia with intrinsic disorder propensity.
Explanation:
