<span>During cell respiration, glucose is broken down in order for the body to gain energy through the use of ADP and ATP. With diabetes, the person's cells are unable to break down the glucose properly, and and overabundance of the sugar in the system leads to negative reactions from the rest of the body.</span>
Answer:(ノ◕ヮ◕)ノ*:・゚✧ The light areas of the Moon are known as the highlands. The dark features, called maria (Latin for seas), are impact basins that were filled with lava between 4.2 and 1.2 billion years ago.
Explanation: (∩^o^)⊃━H~O~P~E T~H~I~S H~E~L~P~S!~
1. A disease cause by a very small genetic change. Most cases result from the deleting of three bases in a gene for a protein called cystic fibrosis transmembrane changes which in a gene's DNA sequence can change proteins by altering their amino acid sequences which may affect one's phenotype.
2. It causes a mutation in the number of chromosomes, either extra chromosomes or missing chromosomes. Nondisjunction during meiosis can cause chromosomal disorders , such as a trisomy 21 (down syndrome) , Tuners syndrome , and Klinefelter's syndrome. It is a monosomy of the X sex chromosome.
Answer: False
Explanation:
Anaerobic means the absence of oxygen while aerobic means the present of oxygen. Anaerobic exercise do not utilize oxygen as energy source, it uses energy from the break down of glucose in the muscles. This exercise is of short length, fast and of high-intensity. A lot of energy is released within a small period of time.
Biologically anaerobic exercise must be fueled using glucose through a process called glycolysis in the muscles cells.
The break down of glucose during high-intensity training without oxygen, producing energy quickly. Because it occurs in the absence of oxygen this process also produces lactate, which is the metabolic fate if glucose in anaerobic condition.
High concentration of lactate is the reason why your muscles get so tired after the energy burst.
Some mutations don't have any noticeable effect on the phenotype of an organism.This can happen in many situations: perhaps the mutation occurs in a stretch of DNA with no function, or perhaps the mutation occurs in a protein-coding region,but ends up not affecting the amino acid sequence of the protein.