Nursing Elites

1. Which type of nutrient requires the most complex and lengthy digestion process?

• A. Carbohydrates
• B. Proteins
• C. Fats
• D. Vitamins

Correct answer: B

Rationale: Proteins require the most complex and lengthy digestion process compared to the other nutrient types provided. When proteins are consumed, they undergo a process where they need to be broken down into amino acids, which are essential building blocks of proteins. This intricate digestion process begins in the stomach aided by stomach acid and enzymes, proceeds to the small intestine where further enzymes break down proteins into amino acids, and concludes with the absorption of these amino acids into the bloodstream for various bodily functions. Carbohydrates and fats also require digestion, but the process for breaking down proteins into amino acids is notably more intricate and time-consuming. In contrast, vitamins do not require digestion in the same manner as proteins, carbohydrates, and fats because they are already in a form that can be readily absorbed by the body.

2. What is the term for a genetic disorder caused by a mutation on the X chromosome?

• A. Autosomal dominant disorder
• B. Autosomal recessive disorder
• C. Sex-linked recessive disorder
• D. Sex-linked dominant disorder

Correct answer: C

Rationale: A genetic disorder caused by a mutation on the X chromosome is termed a sex-linked recessive disorder (Option C). This type of disorder is more commonly seen in males due to their single X chromosome, making them more vulnerable to X-linked mutations. Females have two X chromosomes, providing a protective effect against X-linked disorders.\n- Autosomal dominant disorders (Option A) result from a mutation in one copy of a gene on non-sex chromosomes (autosomes) and are not specifically related to the X chromosome.\n- Autosomal recessive disorders (Option B) occur due to mutations in both copies of a gene on autosomes, not on the X chromosome.\n- Sex-linked dominant disorders (Option D) are rare and lead to more severe symptoms in males as they only require one copy of the mutated gene on the X chromosome to express the disorder. However, this is not the term for a genetic disorder caused by an X chromosome mutation.

3. What is a rod-shaped structure that forms when a single DNA molecule and its associated proteins coil tightly before cell division?

• A. Centromere
• B. Chromatid
• C. Chromosome
• D. Gene

Correct answer: C

Rationale: A chromosome is a rod-shaped structure that forms when a single DNA molecule and its associated proteins coil tightly before cell division. It contains the genetic material and is essential for cell division and replication. The centromere is a specific region of a chromosome that plays a role in cell division. A chromatid is one half of a duplicated chromosome, and a gene is a unit of heredity responsible for specific traits. Therefore, the correct answer is 'Chromosome' as it represents the entire condensed DNA molecule during cell division.

4. Tissues are groups of cells with similar:

• A. Appearance only
• B. Function and structure
• C. Location only
• D. Age only

Correct answer: B

Rationale: Tissues are groups of cells that work together to perform a specific function. They have similar structures that enable them to carry out their specialized functions effectively. Therefore, tissues are defined by both their function and structure, making option B the correct choice. Choices A, C, and D are incorrect because tissues are not solely defined by their appearance, location, or age, but rather by the shared function and structure of the cells within them.

5. Which of the following is NOT a source of genetic variation in a population?

• A. Mutations in genes
• B. Genetic drift (random fluctuations in allele frequencies)
• C. Gene flow (movement of genes between populations)
• D. Blending inheritance (traits of parents are averaged in offspring)

Correct answer: D

Rationale: Rationale: A) Mutations in genes: Mutations are changes in the DNA sequence that can introduce new alleles into a population, leading to genetic variation. B) Genetic drift (random fluctuations in allele frequencies): Genetic drift refers to random changes in allele frequencies in a population, which can lead to genetic variation through chance events. C) Gene flow (movement of genes between populations): Gene flow occurs when individuals move between populations, bringing new alleles with them and increasing genetic variation within populations. D) Blending inheritance (traits of parents are averaged in offspring): Blending inheritance was a historical theory that suggested offspring inherit a blend of traits from their parents, leading to a reduction in genetic variation over time. However, this concept has been disproven by the understanding of Mendelian genetics, where traits are inherited independently and do not blend together. Therefore, blending inheritance does not contribute

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