Answer:
the kidneys excrete salt into the urine when dietary salt levels rise
Explanation:
Hyponatremia is an electrolyte imbalance, with a low level of sodium in the blood. The normal value of sodium in adults is 136 to 145 mEq / L. Sodium is an element, or electrolyte of the blood. Sodium chloride is commonly known as table salt.
Certain conditions can cause decreased sodium in the blood. Specific causes of hyponatremia include:
Water poisoning (water replacement without electrolyte replacement).
Problems in the kidneys, heart or liver.
Medications: such as diuretics, Heparin, certain chemotherapeutics (Aminoglutethimide, Cyclophosphamide and Vincristine).
Conditions related to steroids, hormones or metabolic defects, such as a syndrome that alters the secretion of antidiuretic hormone (SSIHA). If this occurs, you urinate frequently and the kidneys excrete too much sodium. This can result from many conditions, including certain types of lung cancer.
Answer:
C
Explanation:
The production of ATP is greatest at 50o C as indicates by the production of CO2 in the Krebs Cycle
The ICD-10-PCS code is 30240G4.
Firstly, select "Administration" (section 3) because the procedure is the administration of bone marrow to the patient. Secondly, select "Circulatory" (section 30) because it is being administered in a vein (circulatory system). Third, select "Transfusion" (section 302) because it is being done a transfusion of bone marrow. Then select "Central Vein" (section 3024) because that's the place of administration in the circulatory system. Lastly, go to "Bone Marrow" (section 30240G) as that is what's being transfused and then choose "Transfusion of Allogeneic Unspecified Bone Marrow into Central Vein, Open Approach" (<span>30240G4) because it is not specified what type of transfusion it is.</span>
The answer is <span>C.silent.
Nonsense, missense, silent, and frameshift mutations are point mutations. The point mutations are the change in a single nucleotide base on the DNA molecule. In a missense mutation, the change in a single nucleotide base results in a codon coding for a different amino acid. In a nonsense mutation, the change in a single nucleotide results in a stop codon or in a nonsense codon. Frameshift mutation, due to addition or deletion of a base, results in the change of reading frame and totally different translation. In all these cases, the change could lead to different of nonfunctional protein translation.
Silent mutation, on the other, means that change in a nucleotide base will no affect amino acid. It will result in a different codon, but the one that code for the same amino acid, so the same protein will be produced.
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Answer: She will need to learn out how to quantitatively measure mold growth to measure the dependent variable.- last choices
