Answer:
Our eyes can trick our brain in some manner. When the eye see an image, our brain assumes that the image being seen is a image which had been seen in the past. Therefore, our brain is tricked into believing that the image which is being seen is of something which has been visualized before whereas in actual it is a new image. Hence, this is the relationship between seeing of the eyes and perceiving of the brain.
Answer:
D. the 23rd pair of chromosomes
Explanation:
Humans have a total of 23 pairs of chromosomes. Out of a total of 23 pairs, 22 pairs are autosomes. Autosomes are the chromosomes that carry the genes for all the genetic traits but are not involved in the sex determination of the individuals.
The 23rd pair of chromosomes in humans is of sex chromosomes as these chromosomes carry the genes to regulate the gender of the individuals. A human female has two copies of the X chromosome as sex chromosomes while human males have one X and one Y chromosome as their sex chromosomes. The Y chromosome carries "SRY" gene that codes for testes determining factor and regulates the development of testes in the embryo.
Answer:
down
Explanation:
because gravity come from the center of the earth the gravitational pull, pulls us down.
Answer:
Option B
Explanation:
ODD means Oppositional Defiant Disorder while CD means Conduct disorder.
Without initial presence of defiant disorder symptoms, Oppositional defiant disorder are not precursor to the development of conduct disorder.
Oppositional Defiant Disorder and Conduct Disorder are much more predominant in boys than in girls.
According to reseaches carried out,to boys, Oppositional Defiant disorder is a precursor to conduct disorder.
Answer:
The correct option is e
Explanation:
An inversion mutation is a situation in which a sequence of the gene on a chromosome breaks out and rearranges itself from reverse (to the beginning) and then attaches itself back to the point of breakage of the same chromosome.
From the question, mutation changed the gene sequence from ABC*DEFGH to ABC*DGFEH. From this mutation, it can be seen that the gene sequence "EFG" broke-out, rearranged itself from reverse to the beginning as "GFE" and then attached itself back to the points of breakage.
NOTE: This type of inversion is called paracentric inversion since the centromere (represented as * in the question) is not part of the breakage.
