The genetic fault that usually causes colour vision deficiency is passed on in what's known as an X-linked inheritance pattern.
This means:
1) it mainly affects boys, but can affect girls in some cases
2) girls are usually carriers of the genetic fault – this means they can pass it on to their children, but do not have a colour vision deficiency themselves
3) it's usually passed on by a mother to her son – the mother will often be unaffected as she'll normally just be a carrier of the genetic fault
4) fathers with a colour vision deficiency will not have children with the problem unless their partner is a carrier of the genetic fault
5) it can often skip a generation – for example, it may affect a grandfather and their grandson
6) girls are only affected if their father has a colour vision deficiency and their mother is a carrier of the genetic fault
Answer:
The options
A)Damage to cellular mitochondria
B)Increased ATP levels
C)Activation of the p53 protein
D)Apoptosis
The CORRECT ANSWER IS D
D)Apoptosis
Explanation:
The extrinsic pathway of apoptosis includes extracellular signaling proteins which adhere to cell surface molecules known aa death receptors which in turn activates apoptosis.
The aftermath activates endonucleases prompting division of DNA and ultimately cell death.
Apart from the TNF and Fas ligand, primary signaling molecules also promotes the extrinsic pathway, examples of such are the TNF-related apoptosis-inducing ligand (TRAIL); the cytokineinterleukin-1 (IL-1); and lipopolysaccharide (LPS), the endotoxin located in the outer cell membrane of gram-negative bacteria while the activation of the p53 protein, and decreased ATP levels in the intrinsic pathway results in DNA damage.
It's 3,
intraocular is spelt with one c, not two
Water logged? If the soil does not stick together the soil will seperate and water will have easier access to enter
Answer:
B
Explanation:
Crossing over is the process involved during meiosis of two chromosomes sharing genetic information with each other from each parent. This happens so the two daughter cells or sister chromatids have a variety of genetic information and so they are not completely identical. This leads to genetic diversity or variation.