Answer:
Us humans discovered technology to change the way of life at its best, now the technology at every second is changing our's lives. Over the years, technology has successfully attempted to enter our body and change the way of thinking, and the target is human blood and emotions.
Explanation:
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Explanation:
A frameshift mutation is an insertion or deletion in a sequence of DNA which disrupts the way the code is read. It occurs when the codons undergo a disruption through the deletion or insertion of one or multiple nucleotides (given that the number removed or added are not multiples of 3) - this alters the open reading frame; the amino acids produced through translation simply occur in a different sequence.
Further Explanation:
During the process of cell division, spontaneous changes within the genome can arise. These mutations are errors occur when copies of the DNA within the cell are made; mutations may range from small changes called single nucleotide polymorphisms, to large scale deletions, and additions which span multiple genes. There are two types:
- somatic: these only occur within certain cells, and arise from environmental factors such as UV light
- hereditary: occur within germ cells of the parent and later the fertilized egg which forms a zygote; these are present within all cells of the new organism.
Learn more about mutations at brainly.com/question/4602376
Learn more about DNA and RNA at brainly.com/question/2416343?source=aid8411316
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Admitting that the "a" is a capital A for normal pigmentation and "d" is a capital D for dimpled chin, meaning that these are the dominant traits, the fraction expected to be albino with a non-dimpled chin is of 1/16.
When two heterozygous are crossed and two characteristics are being analysed, the offspring quantity that will possess the two recessive traits can be represented by 1/16. This is easily confirmed when a Punnett square is made. Considering that both parents were heterozygous, on both sides of the crossing in the Punnett square, you would have the following alleles' combination: AD, Ad, aD, and ad. The offspring that would be homozygous recessive (aadd) would correspond to only 1/16.
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