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Multiple Choice
A) Proto-oncogenes
B) Tumor-suppressor genes
C) Passenger genes
D) Inhibitor genes
E) Driver genes
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Multiple Choice
A) the observation that certain tumor-suppressor genes and oncogenes are involved in a sequential manner in the development of colon cancer.
B) the fact that proto-oncogenes are widely conserved in evolution.
C) the usual occurrence of retinoblastoma at a young age.
D) the development of a cancer as a result of activation of a single oncogene by any of a variety of mechanisms.
E) the fact that there are many genetic and epigenetic mechanisms that lead to inactivation of the same tumor-suppressor gene.
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A) Carcinoma develops, polyps form, cancer metastasizes.
B) Adenoma forms, polyps form, tumor-suppressor APC gene mutates, cancer metastasizes.
C) Tumor-suppressor APC gene mutates, polyps form, adenoma forms, carcinoma forms.
D) Proto-oncogenes mutate into tumor-suppressor genes, polyps form, cancer metastasizes.
E) Carcinoma becomes metastatic, polyps form, tumor-suppressor APC gene mutates.
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A) DNA sequence undergoes hypermethylation.
B) DNA sequence is nearly intact but is inverted in the new position.
C) gene is released from inhibition by miRNAs.
D) gene is placed under the control of B-cell-specific gene regulatory sequences and is highly expressed.
E) DNA sequence undergoes several point mutations.
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A) p53.
B) BRCA 1.
C) myc.
D) ras.
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A) Retroviral infection
B) Gene duplication
C) Promoter inhibition
D) Retroviral infection and gene duplication are both correct.
E) None of the answers is correct.
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Multiple Choice
A) inversions; duplications
B) recessive; dominant
C) duplications; deletions
D) dominant; recessive
E) deletions; base-pair substitutions
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A) inhibit p53 activity.
B) suppress transcription of tumor-suppressor genes.
C) regulate the progression of G1 to S in the cell cycle.
D) induce cyclin-CDK complex formation.
E) block the initiation of anaphase during the cell cycle.
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A) Duplication
B) Deletion
C) Inversion
D) Translocation
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A) By modifications to cytoskeletal architecture
B) By mutating and rearranging host proto-oncogenes
C) By stimulating overexpression of proto-oncogenes
D) Both by mutating and rearranging host proto-oncogenes and by stimulating overexpression of proto-oncogenes
E) None of the answers is correct.
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Multiple Choice
A) oncogenes
B) proto-oncogenes
C) tumor-suppressor
D) DNA repair
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Multiple Choice
A) Overexpression of angiogenesis-promoting factors
B) Duplication of an oncogene
C) Mutation of a tumor-suppressor gene
D) Both duplication of an oncogene and mutation of a tumor-suppressor gene
E) None of the answers is correct.
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Multiple Choice
A) Deletions
B) Inversions
C) Creation of fusion genes
D) Translocations
E) All of the answers are correct.
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Multiple Choice
A) Primary tumors
B) Secondary tumors
C) Tumor vascularization
D) Decreased DNA repair
E) Increased apoptosis
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