Answer:
yes true cus
Explanation:
virus rely on others cell organism
Answer:
C
Explanation:
The Calvin cycle occurs in three major phases:
1) Carbon fixation; which involves the reaction of CO2 with a phosphorylated Co2 acceptor called Ribulosebiphosphate(RuBp) as catalysed by Rubisco enzyme. Due to the instability of the formed six-carbon compound, it breaks into two molecules of 3-phosphoglycerate (PGA)
2) Reduction; The PGA is phosphorylated by ATP to form 1,3-biphosphoglycerate, which is then reduced by NADPH to form glyceraldehyde-3-phosphate (G3P).
3) Regeneration; The final step, which is very important for the continuity of Calvin cycle is the regeneration of the CO2 acceptor (RUBP). The molecules of G3P are rearranged into molecules of Ribulosephosphate(RuP) by series of complex reactions, which is then phosphorylated by ATP to form RUBP, ready to accept CO2 for the cycle to continue
Is always composed of oceanic lithosphere.
Answer:
75%
Explanation:
Hypophosphatemic rickets is a disorder characterized by hypophosphatemia (low level of phosphate in the blood), defective intestinal absorption of calcium, and rickets (impaired mineralization of cartilaginous growth plates) or osteomalacia (impaired mineralization of the osteoid) unresponsive to vitamin D. It can be inherited or acquired.
When it comes to inheritable hypophosphatemic rickets, the disorder is most often inherited in an X-linked dominant manner. This means that the gene is inherited through the X chromosome and that one dominant allele is enough to cause it.
As the mother is heterozygous for the trait, she has one dominant and one recessive allele (XHXh). The father has one X chromosome, which he inherited from his mother, and as he has the condition, the dominant allele will be present on it (XHY).
This means that, if the child is a girl, she will definitely have the disorder. Girls inherit one X chromosome from each of their parents. Even if she inherited the one with the recessive allele from her mother, she would get the one with the dominant allele from her father.
If the child is a boy, he has a 50% chance to inherit the condition. Boys inherit the Y chromosome from their father and the X chromosome from their mother. As the mother is heterozygous, he can either get the chromosome without the dominant allele or the one with it. This means that there is a 50% chance of inheriting the disorder.
If we say that there are equal chances of this couple having female and male children, when we combine these results, we get a 75% chance of them inheriting hypophosphatemic rickets.
Answer: Hemoglobin
Explanation: It's the protien that carries oxygen in oure blood.