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We would all have many more mutations in our genes if not for the _____.


A) activity of repair enzymes
B) death of all mutant cells,removing them from our bodies
C) fact that everybody carries a "good" allele to counter every "bad" allele
D) fact that dividing cells remove all their mutations when they replicate their DNA
E) fact that mutations tend to cancel each other out,leaving mostly functional genes

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How could a cancerous cell evade apoptosis?


A) The cell responds to environmental signals.
B) The cell goes through the cell cycle too quickly for apoptosis to occur.
C) The cell has a mutation in a checkpoint protein.
D) The cell is stuck in one phase of the cell cycle.
E) Cancerous cells can't evade apoptosis.

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When would you need a gene that can stop the cell cycle?


A) when a mutation occurred and the cell needed time to repair it before continuing
B) when there was no immediate need for more cells
C) when a cell had completed DNA replication
D) A and C only
E) A and B only

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In normal cells,lack of functional tumor suppressors would cause


A) an accumulation of mutations in the DNA.
B) division of damaged cells.
C) cancer,possibly.
D) uncontrolled cell division.
E) All of the above.

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A mutation would most likely be inherited if it is located in a ____ cell.


A) skin
B) body
C) sperm
D) liver
E) All of the above.

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Mutations are


A) always harmful.
B) never neutral.
C) always helpful.
D) never helpful.
E) sometimes harmful,sometimes helpful,and sometimes neutral.

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What kind of mutation causes most types of cancer?


A) mutations in skin cells
B) mutations in transcription factors
C) mutations in blood cells
D) mutations in cell cycle genes
E) None of the above.

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If you mother has a single copy of a harmful BRCA gene,what are the chances you inherited the harmful BRCA allele from her?


A) 0%
B) 25%
C) 50%
D) 75%
E) 100%

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Chemotherapy drugs interfere with


A) cell division.
B) chromosome duplication.
C) spindle formation.
D) chromosome separation during mitosis.
E) All of the above.

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Gene mutations can arise when nucleotides are


A) added to the gene.
B) taken away from the gene.
C) changed within the gene.
D) mismatched within the gene.
E) All of the above.

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A gene found in a somatic cell is mutated.The resulting protein regulates mitosis but now has a different 3D shape.What is a likely result?


A) germ-line mutations
B) hereditary mutations
C) cancer
D) down syndrome
E) cystic fibrosis

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Bob and Linda are a newly married couple.They hope to have a child but are having trouble getting pregnant.They visit a fertility clinic,where they receive a variety of tests.One test shows that Bob is healthy but carries a single disease-causing allele for CFTR (the gene that can cause cystic fibrosis) ,but Linda does not.This means that


A) Bob's DNA sequence for CFTR is different from Linda's.
B) Bob has two different versions of the CFTR gene.
C) Linda does not have any copies of the CFTR gene.
D) Bob is unable to ever have children.
E) Both A and B

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The cell cycle checkpoints are responsible for checking that the cell is prepared to move on to the next stage in cell division.For example,the G1-to-S checkpoint ensures that the cell has all the components and signals necessary to go on to S phase and that the appropriate signals are present.The G2 checkpoint checks whether the


A) chromosomes have been separated properly.
B) DNA has been replicated properly.
C) chromosomes have aligned properly.
D) DNA has decondensed.
E) cell organelles have duplicated properly.

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What kinds of preventative measures are available for individuals who have a strong genetic predisposition to breast cancer?


A) genetic counseling,so they know the risks
B) regular medical screening for cancer
C) a healthy lifestyle,a good diet,and an exercise regimen
D) prophylactic surgery
E) All of the above.

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If an individual has a germ cell mutation,which of these is a possible source of that mutation?


A) excessive sun exposure
B) a maternal or paternal allele
C) a paternal allele only
D) a maternal allele only
E) overuse of alcohol

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Metastasis is


A) an effective form of treatment for cancer.
B) part of cell division,when chromosomes line up.
C) a state of rest for the cell,between divisions.
D) a state of active cell division.
E) the spread of cancer from one location in the body to another.

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The most common cancer among women is


A) prostate cancer.
B) breast cancer.
C) ovarian cancer.
D) nonmelanoma skin cancer.
E) lung cancer.

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Why is a person who has inherited one copy of a harmful BRCA allele much more likely to have early-onset breast cancer or ovarian cancer than a person with two functioning alleles?


A) Apoptosis is increased,as the tumor suppressors are not functioning.
B) Cell growth is accelerated,as oncogenes are switched on.
C) With the increase of BRCA protein,apoptosis is induced and cell death occurs.
D) Mutations accumulate as DNA repair is slowed and cell growth may accelerate.
E) Cells fail to enter apoptosis and eventually become a tumor.

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Mutations that cause the cell to divide rapidly,even in the absence of a signal to divide,are usually mutations of


A) proto-oncogenes.
B) tumor-suppressor genes.
C) DNA polymerase.
D) cell-surface proteins.
E) DNA-repair enzymes.

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What is the increased risk of ovarian cancer by age 70 if you have one copy of a deleterious BRCA2 allele when compared to the general population? What is the increased risk of ovarian cancer by age 70 if you have one copy of a deleterious BRCA2 allele when compared to the general population?   A)  1.3% B)  9.7% C)  11% D)  39% E)  55%-65%


A) 1.3%
B) 9.7%
C) 11%
D) 39%
E) 55%-65%

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