A) Sickle-cell anemia
B) Huntington's disease
C) Duchenne muscular dystrophy
D) Alzheimer's disease
E) Fragile-X syndrome
Correct Answer
verified
Multiple Choice
A) Somatic mutations occur during sex cell formation.
B) Germ line mutations occur during mitosis.
C) Somatic mutations are passed on to sexually produced offspring.
D) An example of a germ line mutation is hemophilia.
E) All of the above
Correct Answer
verified
Multiple Choice
A) silent mutations are usually found in noncoding regions of DNA.
B) the genetic code is ambiguous.
C) silent mutations are recessive, and the presence of the dominant allele will result in a functional protein.
D) silent mutations are conditional mutagens, and their phenotypes are only altered under very restrictive conditions.
E) only a single base is involved in a series of thousands of nucleotides.
Correct Answer
verified
Multiple Choice
A) Homologous and antisense RNA recombination
B) Pharming and phishing
C) Restriction digestion and gel electrophoresis
D) Gel electrophoresis and creation of expression vectors
E) Homologous recombination and the construction of gene libraries
Correct Answer
verified
Multiple Choice
A) is very expensive.
B) detects phenylketones in urine.
C) has not led to the prevention of mental retardation resulting from this disorder.
D) should be done during the second or third day of an infant's life.
E) uses bacterial growth to detect excess phenylketones in blood.
Correct Answer
verified
Short Answer
Correct Answer
verified
View Answer
Multiple Choice
A) triplets bind to mRNAs of other genes.
B) cytosines in the repeats are more likely to be methylated, leading to inactivation of the gene.
C) triplets cause genomic imprinting.
D) triplets make the gene so large that its mRNA cannot be transported properly.
E) triplets cause the protein to fold incorrectly.
Correct Answer
verified
Multiple Choice
A) are dominant mutations that are expressed in wild-type cells.
B) are dominant mutations that are expressed in mutant cells.
C) are the cause of continuous division in cancer cells.
D) can be analyzed only under restrictive conditions.
E) are expressed only with the appropriate environmental signals.
Correct Answer
verified
Multiple Choice
A) each person is unlikely to be a carrier for harmful alleles.
B) genetic diseases are usually sex-linked and so uncommon in females.
C) genetic diseases are always dominant.
D) two parents probably do not carry the same recessive alleles.
E) mutation rates in humans are low.
Correct Answer
verified
Multiple Choice
A) DNA polymerase
B) Ligase
C) Lactase
D) Reverse transcriptase
E) Methylase
Correct Answer
verified
Short Answer
Correct Answer
verified
Multiple Choice
A) expanding triplet repeats that occur during DNA synthesis.
B) point mutations that do not change the amino acid sequence of the gene.
C) prion diseases such as "mad cow" in humans.
D) mutations in restriction sites in the DNA.
E) Both a and d
Correct Answer
verified
Multiple Choice
A) a clotting factor in the blood is nonfunctional.
B) the sixth amino acid is changed from a valine to a glutamic acid.
C) the sixth amino acid is changed to a stop codon.
D) hemoglobin builds up in the red blood cells.
E) the structure of -globin is altered, and the hemoglobin protein forms aggregates in the red blood cells.
Correct Answer
verified
Multiple Choice
A) result in a single amino acid substitution.
B) almost always lead to loss of function.
C) result from only single or double base deletions of a base(s) .
D) cause the ribosome to misread mRNA.
E) result only from the addition of an extra base.
Correct Answer
verified
Multiple Choice
A) involves positional cloning.
B) uses PCR and RFLPs to examine their DNA.
C) tests for the level of phenylalanine in their blood.
D) requires constructing a gene library.
E) None of the above
Correct Answer
verified
Multiple Choice
A) the new sequence of DNA must become part of the patient's genome.
B) the gene must be precisely inserted into the patient's cells.
C) the gene must be attached to a promoter that will express it.
D) Both a and b
E) a, b, and c
Correct Answer
verified
Multiple Choice
A) muscle atrophy.
B) kidney failure.
C) mental retardation.
D) skeletal problems.
E) None of the above
Correct Answer
verified
Multiple Choice
A) dysfunctional enzymes.
B) abnormal receptor proteins.
C) abnormal transport proteins.
D) abnormal structural proteins.
E) All of the above
Correct Answer
verified
Multiple Choice
A) negatively; methyl
B) negatively; phosphate
C) negatively; carbon
D) positively; methyl
E) positively; phosphate
Correct Answer
verified
Multiple Choice
A) Deletion of the last 100 codons of gene X
B) A duplication of gene X
C) An inversion of the last 100 codons of gene X
D) A translocation of the last 100 codons of gene X to another chromosome
E) None of the above
Correct Answer
verified
Showing 121 - 140 of 141
Related Exams