That is correct, a good description of the HYPODERMIS. Hence many syringes get the name "hypodermic" needles.
Answer:
b. Frank received the mutant chromosome from his father. Nondisjunction occurred in his father during the first meiotic division.
Explanation:
As you can see in the question above, Frank has Klinefelter syndrome which causes him to have normal skin patches and skin patches without sweat glands. Her mother has completely normal hair, which may indicate that the defective gene was not supplied by her. In addition, Frank's father has anhydrotic ectodermal dysplasia, an X-linked condition where the skin does not contain sweat glands.
Although Frank's father's defective gene is linked to the X chromosome, it is likely that Frank inherited the defective gene from his country. This may have occurred because during meiosis I, his father's genes did not show disjunction. As a result, Frank presents a mosaic of his phenotype, because an inactivation of the X chromosome occurred.
Answer:
A. maintenance of axons is not a cellular activity associated with microtubules.
Explanation:
Microtubules are hollow, bead-like, tiny tubular structure that helps cells maintain its shapes. Together with microfilaments and intermediate filaments, they form part of the cell's cytoskeleton. Microtubules also contributes to the cell movement or cytokinesis that includes muscle contractions in muscle cells. Microtubules also replicated chromosomes to opposite ends of a cell during cell division. Microtubules also contribute to the parts of the cell that help it move and are structural elements of cilia, centrioles and flagella. A bundle of microtubules makes up an axonemal structure of cilia and flagella.
This is true. There are a few websites online that talk about how it happens, I suggest looking them up.
