ATI TEAS 7
TEAS 7 science study guide free
1. Which nitrogenous bases pair with each other in DNA?
- A. A-G and T-C
- B. A-T and C-G
- C. A-T and T-T
- D. C-C and G-G
Correct answer: B
Rationale: In DNA, nitrogenous bases pair with each other in a specific manner known as complementary base pairing. Adenine (A) always pairs with Thymine (T), and Cytosine (C) always pairs with Guanine (G). This pairing is essential for maintaining the structure and function of DNA. Option B is the correct answer as it correctly identifies the nitrogenous bases that pair with each other in DNA. Choices A, C, and D are incorrect because they do not follow the established base pairing rules in DNA. A-T and C-G are the complementary base pairs in DNA, ensuring the stability and replication fidelity of the genetic material.
2. Which of the following is NOT a characteristic of mitosis?
- A. The replication of DNA
- B. The condensation of chromosomes
- C. The separation of sister chromatids
- D. The formation of haploid cells
Correct answer: D
Rationale: Rationale: A) The replication of DNA is a characteristic of mitosis. Before cell division occurs, the DNA is replicated to ensure that each daughter cell receives a complete set of genetic information. B) The condensation of chromosomes is a characteristic of mitosis. During mitosis, the chromosomes condense and become visible under a microscope as distinct structures. C) The separation of sister chromatids is a crucial step in mitosis. During anaphase, the sister chromatids are pulled apart and move to opposite poles of the cell to ensure that each daughter cell receives a complete set of chromosomes. D) The formation of haploid cells is NOT a characteristic of mitosis. Mitosis results in the formation of two identical diploid daughter cells, each containing the same number of chromosomes as the parent cell. Haploid cells are typically formed through the process of meiosis, not mitosis.
3. Which organ is primarily responsible for detoxification in the body?
- A. Kidney
- B. Liver
- C. Lung
- D. Heart
Correct answer: B
Rationale: The liver is the primary organ responsible for detoxifying chemicals and metabolizing drugs in the body. It plays a crucial role in breaking down toxins, filtering blood, and producing bile, making it essential for overall detoxification processes. The kidney primarily filters waste and excess substances from the blood to form urine. Lungs are responsible for gas exchange, not detoxification. The heart is responsible for pumping blood and does not play a direct role in detoxification processes.
4. Which of the following terms refers to the degeneration of nerve tissue?
- A. Potentiation
- B. Demyelination
- C. Reuptake
- D. Neurogenesis
Correct answer: B
Rationale: Demyelination specifically refers to the degeneration of the myelin sheath that covers nerve fibers. When demyelination occurs, nerve function and communication can be impaired. Potentiation involves the strengthening of synaptic connections, reuptake is the reabsorption process of neurotransmitters by the presynaptic neuron, and neurogenesis is the generation of new neurons. Therefore, the correct term for the degeneration of nerve tissue among the options provided is demyelination.
5. What is the term for a genetic disorder caused by a mutation in a mitochondrial gene?
- A. Autosomal dominant disorder
- B. Autosomal recessive disorder
- C. Sex-linked disorder
- D. Mitochondrial disorder
Correct answer: D
Rationale: A) Autosomal dominant disorder: This type of genetic disorder is caused by a mutation in one copy of an autosomal gene. It is not related to mitochondrial gene mutations. B) Autosomal recessive disorder: This type of genetic disorder is caused by mutations in both copies of an autosomal gene. It is not related to mitochondrial gene mutations. C) Sex-linked disorder: This type of genetic disorder is caused by mutations in genes located on the sex chromosomes (X or Y). It is not related to mitochondrial gene mutations. D) Mitochondrial disorder: Mitochondrial disorders are genetic disorders caused by mutations in genes located in the mitochondria, the energy-producing structures within cells. These disorders are inherited maternally and can affect various organs and systems in the body due to the role of mitochondria in energy production.
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