Answer:
Methemoglobinemia
Explanation:
Methemoglobinemia (also known as the blue baby syndrome), is a condition with multiple etiologies which is associated with the lack of oxygen in the blood. This syndrome affects the function of red blood cells by altering the amount of hemoglobin protein, which carries and distributes oxygen to the body. Methemoglobinemia may be acquired by exposure to drugs and/or toxins. In this regard, it has been shown that high levels of nitrates in the water may induce this syndrome in infants.
Answer:
option A
Explanation:
The protein specific sequence also known as the primary sequence is determined by the sequence of its amino acids linked together by peptide bonds. The sequences of amino acids determine the proteins that will eventually be synthesized. This proteins becomes functional when correct folding pattern/ native conformation of the protein occurs which determines the shape of the proteins. peptide bonds hold the amino acid sequences together, hydrogen bonds involving components of the peptide bonds allow for the existence of the secondary structure either the alpha helix or the beta pleated sheets and then disulphide bonds and other type of bonds helps in the folding of the protein to become a functional protein.
The answer to your problem or question is C pleas like this
Answer:
Habitat is a place in which organisms live, and niche is the way in which an organism fits into its habitat
Answer:
A) Chromosomes are made of DNA
C) Alleles are the different forms of a gene that can exist
D) Chromosomes contain genes that control the inheritance of traits.
Explanation:
Chromosomes are long molecules of deoxyribonucleic acid (DNA) that contain part (or all) of the genetic material of an organism. Humans contain 46 chromosomes organized in 23 pairs of homologous chromosomes (22 pairs of autosomal chromosomes and one pair of sex chromosomes, X and Y). Moreover, a gene is a physical segment of a chromosome that contains the information to encode a protein. Alleles are different forms of a gene (i.e., gene variants) that may be caused by mutations or genetic recombination. Humans are diploid organisms (2N: 46), and therefore we have two copies of each gene (alleles), one on each homologous chromosome.
