This statement is true.
In the case of autosomal dominant disease, the person is either homozygous (which is very rare) or heterozygous. On the molecular level, either the mutation produced a new deleterious protein for the organism, or the mutation affected an existing protein in the physiological state and that a 50% activity is not enough to compensate for the needs. of the body.
In case of autosomal recessive disease, the sick person is always homozygous. If the two loci each have a different mutant allele, it is called a "composite heterozygote". People with autosomal recessive inheritance disorder have "mandatory heterozygote" parents.
Arthropods. im not sure if that helps but, thats what they are called.
Answer:
Profase - Metafase - Anafase - Telofase - Citocinesis
Explanation:
Estas fases ocurren en orden estrictamente secuencial y la citocinesis —el proceso de dividir el contenido de la célula para hacer dos nuevas células— comienza en la anafase o telofase. Etapas de la mitosis: profase, metafase, anafase y telofase. La citocinesis típicamente se superpone con la anafase o telofase.
Cancer is the rapid, uncontrollable division of cells.
I’d talk about how enzymes have that induced fit model. A substrate is unique to that specific enzyme. The substrate binds to the enzymes active site (or sometimes allosteric site) which in turn alters the conformation or shape of that particular enzyme
