A) Telomerase
B) Transcription factors controlling cell growth
C) Inhibitors of apoptosis
D) Growth factor receptor tyrosine kinases
E) Cell cycle checkpoint proteins
Correct Answer
verified
Multiple Choice
A) Homogeneously stained regions
B) Microsatellite instability
C) Double minute chromosomes
D) A and B
E) A and C
Correct Answer
verified
Multiple Choice
A) Telomerase
B) Cell cycle checkpoint genes
C) Transfer RNAs (tRNAs)
D) Micro RNAs (miRNAs)
E) Ribosomal RNA (rRNAs)
Correct Answer
verified
Multiple Choice
A) Cellular starvation
B) Shortened telomeres
C) DNA damage
D) Cellular contact
E) Phosphate levels
Correct Answer
verified
Multiple Choice
A) Ricin
B) Colchicine
C) Aflatoxin
D) Curare
E) β-amanitin
Correct Answer
verified
Multiple Choice
A) It can go on to produce any type of cancer
B) It gives rise to multiple lineages of genetically unstable cells that can each undergo additional mutation
C) It is resistant to chemotherapy
D) It contains all genetic variation found in the tumor
E) It is the cell that is inherited from a parent in Mendelian cancers
Correct Answer
verified
Multiple Choice
A) Family history
B) Clinical information on the cancer
C) Microsatellite instability testing
D) Staining for the presence of mismatch repair proteins
E) All of the above
Correct Answer
verified
Multiple Choice
A) Caspase activation
B) Excessive recombination
C) Microsatellite instability
D) DNA fragmentation
E) Nondisjunction
Correct Answer
verified
Multiple Choice
A) Loss of function, gain of function
B) Gain of function, loss of function
C) Duplication, loss of function
D) Loss of function, duplication
E) Deletion, duplication
Correct Answer
verified
Multiple Choice
A) Gene amplification
B) Nonhomologous recombination
C) Splice mutations
D) Interstitial deletions
E) Inversions
Correct Answer
verified
Multiple Choice
A) Always inherited
B) Always somatic
C) Sometimes somatic
D) An activating mutation
E) A truncating mutation
Correct Answer
verified
Multiple Choice
A) Inversion
B) Interstitial deletion
C) Duplication
D) Translocation
E) Terminal deletion
Correct Answer
verified
Multiple Choice
A) p53
B) RB
C) CYP2D6
D) FAS
E) MLH1
Correct Answer
verified
Multiple Choice
A) 5%
B) 10%
C) 25%
D) 50%
E) 100%
Correct Answer
verified
Multiple Choice
A) Methylation of the BRCA1 or BRCA2 promoter
B) Acetylation of the BRCA2 or BRCA2 promoter
C) Deletion of the tumor-associated transplantation antigen (TATA) box in BRCA1 or BRCA2
D) Deletion of a BRCA1 or BRCA2 enhancer
E) Nonsense mutation in BRCA2 or BRCA2
Correct Answer
verified
Multiple Choice
A) Protooncogene
B) Oncogene
C) Tumor suppressor
D) Mismatch repair protein
E) Telomerase
Correct Answer
verified
Multiple Choice
A) It puts a protooncogene downstream of a strong promoter
B) It fuses a protooncogene with another protein and alters its activity
C) It deletes its opposing tumor suppressor
D) It deletes a regulatory region for the gene
E) It removes its 3'-untranslated region (UTR)
Correct Answer
verified
Multiple Choice
A) It puts a protooncogene downstream of a strong promoter
B) It fuses a protooncogene with another protein and alters its activity
C) It deletes its opposing tumor suppressor
D) It deletes a regulatory region for the gene
E) It removes its 3' UTR
Correct Answer
verified
Multiple Choice
A) Autosomal recessive with nearly complete penetrance
B) Autosomal dominant with nearly complete penetrance
C) Autosomal recessive with incomplete penetrance
D) Autosomal dominant with incomplete penetrance
E) X linked recessive
Correct Answer
verified
Multiple Choice
A) Genes involved in recombination
B) Mismatch repair genes
C) Receptor tyrosine kinases
D) G proteins
E) Transcription factors
Correct Answer
verified
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