The liver is the largest internal organ, because it has many important functions such as making bile, collecting circulated blood, and processing chemicals.
Answer:
The organisms homeostasis
Answer:
Explanation:
Humans are increasingly influencing the climate and the earth's temperature by burning fossil fuels, cutting down rainforests and farming livestock. This adds enormous amounts of greenhouse gases to those naturally occurring in the atmosphere, increasing the greenhouse effect and global warming
Answer:
Explanation:
The Genotype of the woman is XCbXN
The man XNY
Since the allele for the color blindness is carried on one of the X -chromosomes of the carrier mother, then the male children will be color blind or carrier deopending on the defective gene they inherited. Since they will receive the defective or normal allele from the mothers,but the female will carriers or normal because they will inherit either defective allele or normal allele from the mother,but normal X allele from the father.
Assuming the colorbind gene was inherited by One of the boys, and the girls take the defective genes
1. XNY vs XCbXN.Then the one of the boys will be colorblind and the one of girls will be carriers. XNXCb, XNXN, XCbY,XNY 50 %
2.If the two boys take the effective genes from the mothers. and none of the girls take the defective alelle
Then the two boys will be colorblind and the girls will be carrries XcbY,XcbY and XNXN XNXN.(normal girls).
The proportions that will be the females since the girls can only take the defective allele from one of the normal and defective allele from the mother. Assuming the girls take the defective allele from the mothers and take normal from the father,they will all be carriers,since the X of the father is normal.
They can not have a color blind girl.Since the father is normal It takes two colorblind X-chromosome to give a girl.
Answer: Germline mutation
A germline mutation is a mutation in the fully developed germ cells (sperm and ovum). These defective mutated cells fuse to form zygote. The zygote rapidly produces all somatic and germline cells in the offsprings which are also mutated. Therefore, mutation is transmitted from parents to offsprings. Cystic fibrosis is a result of germline mutation. This disease is hereditary in nature passes from parents to the offsprings. If a child receives CFTR (cystic fibrosis transmembrane conductance regulator) mutated gene from both the parents than the child will be affected by the symptoms of this disease. If the child receives a single copy of CFTR gene from either of the parent than the child will be the carrier of disease.The mutated gene may be present in the germline cells of the parent or on all the body cells.
