Answer:
c. Glutamine is metabolized by deamination, oxidation, and acidification.
Explanation:
Bicarbonate ions are an important part of bicarbonate buffer system which helps to maintain the pH of blood. Whenever blood starts to become acidic, bicarbonate ions increase to neutralize its effect. Their concentration can be increased by many mechanisms, for example tubular reabsorption.
However, glutamine catabolism does not replenish bicarbonate ions, in fact it does the exact opposite. Kidney generates ammonium ions by catabolism of glutamine which are excreted in the urine. This process also facilitates the excretion of bicarbonate ions.
I think it is a daisy bc they are small
The carbon cycle is when carbon travels from the atmosphere into organisms and the earth then back into the atmosphere. Within the ecosystem it helps plants make food, by taking carbon dioxide from the air. The animals eat the food, the carbon is either stored in their bodies or released as carbon dioxide (CO2) through the process of 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
b. proteins provide most of the body's material for building and repairing cells~
