Answer: here you go It is the answer
Explanation: Photosynthesis takes place inside plant cells in small things called chloroplasts. Chloroplasts contain a green substance called chlorophyll. Below are the other parts of the cell that work with the chloroplast to make photosynthesis happen.
Fog occurs in inlets and bays when the water temperature is warm enough for water vapor to evaporate off of these water bodies and the external temperature is cool enough close to the bodies of water for condensation to occur. The water vapor from the water bodies contain nuclei by which the clouds can form and if the air is cool enough this will occur over the water body relatively quickly. This may occur more in the early mornings or late afternoons.
Answer:
Comes from carbon in glucose and the oxygen used in cellular respiration
Explanation:
Carbon dioxide is a waste product of cellular respiration
Answer:
The correct answer is ''All three are caused by disparate genes, but each gene was found to contain repeats of a unique trinucleotide sequence.''
Explanation:
Four groups of trinucleotide repeats related to DNA expansion have been characterized in the human genome. CGGI GCC, CAGIGTC, CTGIGAC and recently GW CTT sequences. The CGGl GCC sequences are usually located in the noncoding regions of different genes and when expanded they associate with fragile sites on the chromosomes. The CAGIGTC repeats are part of the coding region and are related to different neurodegenerative disorders. You can try to make a classification depending on the unit that is repeated, having on one side a group that are caused by repeats of the CAG trinucleotide (cytosine, adenine, guanine). Huntington's disease (HD) is a progressive disorder of motor, cognitive and psychic function. The disease is inherited in an autosomal dominant manner, and is caused by the expansion of CAG trinucleotide repeats in exon 1 of the gene called huntingtin (HTT or IT-15). Unstable mutations have also been found in which the repeat unit does not is composed of three nucleotides, if not four, such as type 2 myotonic dystrophy, where the tetranucleotide CCTG repeats. Fragile X Syndrome consists of an abnormal expansion of the cytosine-guanine-guanine trinucleotide (CGG) in the FMR1 gene, which prevents intellectual disability and also influences the formation of connective tissue
