Nursing Elites

1. Dense irregular connective tissue, found in tendons and ligaments, provides:

• A. Flexibility
• B. Lubrication
• C. Insulation
• D. Tensile strength

Correct answer: D

Rationale: Dense irregular connective tissue, found in tendons and ligaments, provides tensile strength. Tendons and ligaments need to withstand tension and forces acting upon them, and the dense irregular connective tissue helps provide this strength and support. Choice A, flexibility, is incorrect because tendons and ligaments primarily provide support and stability rather than flexibility. Choice B, lubrication, is not the main function of dense irregular connective tissue in tendons and ligaments. Choice C, insulation, is also incorrect as this tissue type is not primarily involved in providing insulation.

2. Immunoglobulin G (IgG) is the most abundant antibody type, responsible for:

• A. Immediate allergic reactions
• B. Neutralizing toxins and viruses
• C. Activating other immune cells
• D. Protecting newborns from infections

Correct answer: B

Rationale: Immunoglobulin G (IgG) is indeed the most prevalent antibody type in the blood and tissue fluids. Its primary functions include neutralizing toxins and viruses, promoting phagocytosis, and activating the complement system. IgG plays a crucial role in long-term immunity and provides passive immunity to newborns by crossing the placenta, safeguarding them from infections. Immediate allergic reactions are mainly mediated by IgE, not IgG. While IgM is known for activating other immune cells, IgG focuses on other key functions within the immune response, such as neutralizing pathogens and enhancing phagocytosis. Therefore, the correct answer is B, as IgG is primarily involved in neutralizing toxins and viruses, rather than the other options presented.

3. What is the ultimate end product of glucose breakdown in glycolysis?

• A. ATP
• B. NADPH
• C. Pyruvic acid
• D. Oxygen

Correct answer: C

Rationale: The ultimate end product of glucose breakdown in glycolysis is pyruvic acid. During glycolysis, glucose is broken down into pyruvic acid through a series of enzymatic reactions. ATP is produced as an energy carrier during glycolysis, but it is not the final end product. NADPH is not a direct product of glycolysis; it is mainly produced in the pentose phosphate pathway. Oxygen is not a product of glycolysis but is used as an electron acceptor in the electron transport chain of cellular respiration.

4. During REM sleep, which type of brain wave activity is often seen and associated with dreaming?

• A. Delta waves
• B. Alpha waves
• C. Beta waves
• D. Theta waves

Correct answer: D

Rationale: Theta waves are the correct answer as they are often seen during REM (rapid eye movement) sleep, the stage of sleep closely related to dreaming. Theta waves have a frequency of 4-7 Hz and are typically present during deep relaxation, meditation, and light sleep stages. Delta waves (choice A) are associated with deep sleep stages, not REM sleep. Alpha waves (choice B) are present during wakefulness and relaxation but not predominantly during REM sleep. Beta waves (choice C) are associated with alertness, problem-solving, and active thinking, not specifically with REM sleep or dreaming.

5. 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.

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