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Multiple Choice
A) It blocks protein synthesis.
B) It disrupts the Golgi apparatus.
C) It increases the pH of the lysosome.
D) It blocks TLR signaling.
E) All of the answers are correct.
Correct Answer
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Multiple Choice
A) 1:1.
B) 1:2.
C) 1:4.
D) 1:8.
E) 1:16.
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Multiple Choice
A) A T-cell clone is deleted when it binds too tightly to self-MHC.
B) A T-cell clone responds more vigorously to a self-peptide than a foreign peptide.
C) A T-cell clone recognizes foreign MHC.
D) A T-cell clone only recognizes foreign peptides when presented by self-MHC.
E) All of the answers are correct.
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Multiple Choice
A) The Golgi apparatus
B) Outside the cell
C) The endosome/lysosome
D) The cytoplasm
E) The chloroplast
Correct Answer
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Multiple Choice
A) None.Only APC express class I.
B) One
C) Two
D) Three
E) Six
Correct Answer
verified
Multiple Choice
A) Dendritic cells
B) Macrophages
C) Erythrocytes
D) Intestinal epithelial cells
E) Basophils
Correct Answer
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Essay
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Multiple Choice
A) Peptides exported from the ER by TAP > peptides are digested by the proteasome > peptides are loaded onto class I > class I is exported to the cell surface
B) Proteins are digested by the proteasome > peptides are imported into the ER by TAP > peptides are loaded onto MHC class I > class I is exported to the cell surface
C) MHC class I moves from the cell surface to the lysosome by endocytosis > class I bound peptides are replaced with antigenic peptides in the lysosome > class I returns to the cell surface
D) Proteins are degraded by TAP > peptides are imported into the lysosome by the proteasome > peptide-MHC class I complexes are exported to the cell surface
E) MHC class I is transported to the ER by TAP > proteins in the ER are degraded into peptides by the proteasome > peptides bind MHC class I in the ER, and the complex is exported to the cell surface
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Multiple Choice
A) in the peptide-binding groove.
B) in the transmembrane domain.
C) in the coreceptor contact residues.
D) in the framework region.
E) All of the answers are correct.
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Multiple Choice
A) expression of paternal MHC class I molecules.
B) expression of paternal MHC class II molecules.
C) expression of nonclassical class I molecules.
D) expression of nonclassical class II molecules.
E) expression of class III MHC molecules.
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Essay
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Multiple Choice
A) variety of peptides that bind to MHC.
B) variety of BCRs that are expressed on mature B cells.
C) rate of somatic hypermutation.
D) number of antigen-presenting cells.
E) transmembrane domain.
Correct Answer
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Essay
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Multiple Choice
A) An endogenous peptide being presented on MHC class I
B) An exogenous peptide being presented on MHC class I
C) An endogenous peptide being presented on MHC class II
D) An exogenous peptide being presented on MHC class II
E) A B-cell antigen being presented to a T cell
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Multiple Choice
A) cells with no class II MHC.
B) cells with no DO.
C) cells with class II MHC only bound with CLIP.
D) cells with class II MHC bound with a variety of self-antigens.
E) a deficiency in CD8+ T cells.
Correct Answer
verified
Multiple Choice
A) A TCR contact residue
B) A residue in the transmembrane domain of an envelope protein
C) A residue in the DNA-binding domain
D) An anchor residue
E) An amino acid on the surface of the virus
Correct Answer
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Essay
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Essay
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