Answer:
<u>The process of photosynthesis occurs in the chloroplast</u>. Photosynthesis can be described as a process in which plants convert water and carbon dioxide into glucose and oxygen. Oxygen is the by-product of the reaction. The energy for this reaction is taken by the chloroplast by trapping light energy of the Sun.
The reaction for photosynthesis can be written as:
6CO2 + 6H2O → C6H12O6 + 6O2
<u>The process of cellular respiration takes place in the mitochondria.</u> Respiration can be described as a process in which glucose and oxygen get converted into carbon dioxide and water. Energy is released by this process which is used for many cellular activities. Hence, mitochondria is known as the powerhouse of a cell.
The reaction of cellular respiration can be summed up as:
C 6 H 12 O 6 + 6 O 2 --> 6 CO 2 + 6 H 2 O + ATP
Both, these processes provide energy for the working of cells.
STI stands for Sexually transmitted infection.
I would go with C because it’s the only that makes any logical sense. All the others except B are fillers
Answer:
Lake Titicaca
Explanation:
Which is located in peru.
Answer: Cystic Fibrosis
Explanation:
Cystic fibrosis (abbreviated CF) is an autosomal recessive genetic disease that mainly affects the lungs, and to a lesser extent the pancreas, liver and intestine, causing an abnormally thick, sticky mucus to build up in these areas. This mucus collects in the airways of the lungs and pancreas. The main cause of morbidity and mortality is pulmonary involvement, which accounts for 95% of deaths, mainly due to repeated infections caused by bronchial obstruction due to the secretion of very thick mucus.
This build up of mucus causes life-threatening lung infections and serious digestive problems. It is one of the most common types of chronic lung disease in children and young adults, and is a life-threatening disorder; patients often die from lung infections due to <em>Pseudomonas</em> or <em>Staphylococcus</em>.
<u>It is a hereditary disease produced by a mutation in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This protein is involved in the passage of chlorine ion through cell membranes and its deficiency alters the production of sweat, gastric juices and mucus. </u>The disease develops when neither allele is functional. Over 1500 mutations have been described for this disease, most of which are small deletions or point mutations; less than 1% are due to mutations in the promoter or chromosomal rearrangements. However, many people carry the CF gene, but do not have any symptoms. This is because a person with this disease must inherit 2 defective genes, 1 from each parent.
<u>There is no curative treatment, however there are treatments that allow the improvement of symptoms and extend life expectancy. In severe cases, the worsening of the disease may necessitate a lung transplant.</u>
