That sucks for you sorry that this doesn’t help you
Answer:
a. 50%
Explanation:
<em>BRCA1 genes is a tumor supressor gene whose harmful mutation can cause hereditary breast ovarian cancer syndrome in both males and females. The BRCA actually stands for breast cancer.</em>
<em>Mutation in BRCA1 gene is heritable and every progeny of a carrier parent irrespective of the sex has a 50% chance of inheriting the trait from such parent, be it from the mother or the father.</em>
Hence, the correct option is a.
spongy bone is found in the bones of the skull, sternum, vertebrae, the pelvis, the lining of the marrow cavity and the epiphysis.
Answer:
Having considered how an appropriate primary immune response is mounted to pathogens in both the peripheral lymphoid system and the mucosa-associated lymphoid tissues, we now turn to immunological memory, which is a feature of both compartments. Perhaps the most important consequence of an adaptive immune response is the establishment of a state of immunological memory. Immunological memory is the ability of the immune system to respond more rapidly and effectively to pathogens that have been encountered previously, and reflects the preexistence of a clonally expanded population of antigen-specific lymphocytes. Memory responses, which are called secondary, tertiary, and so on, depending on the number of exposures to antigen, also differ qualitatively from primary responses. This is particularly clear in the case of the antibody response, where the characteristics of antibodies produced in secondary and subsequent responses are distinct from those produced in the primary response to the same antigen. Memory T-cell responses have been harder to study, but can also be distinguished from the responses of naive or effector T cells. The principal focus of this section will be the altered character of memory responses, although we will also discuss emerging explanations of how immunological memory persists after exposure to antigen. A long-standing debate about whether specific memory is maintained by distinct populations of long-lived memory cells that can persist without residual antigen, or by lymphocytes that are under perpetual stimulation by residual antigen, appears to have been settled in favor of the former hypothesis.
