TLS Online TPP Program
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TLS Online TPP Program
#Question id: 31147
#Unit 2. Cellular Organization
When a mutant protein disulfide isomerase lacking KDEL residues is synthesized in cultured fibroblasts, resulting:
TLS Online TPP Program
#Question id: 31148
#Unit 2. Cellular Organization
KDEL receptor, located in the different locations except?
TLS Online TPP Program
#Question id: 31149
#Unit 2. Cellular Organization
KDEL receptor and other membrane proteins that are transported Golgi to ER contain:
TLS Online TPP Program
#Question id: 31150
#Unit 2. Cellular Organization
The most common CFTR mutation is a deletion of a phenylalanine at position 508 in the protein sequence. This mutation prevents:
TLS Online TPP Program
#Question id: 31151
#Unit 2. Cellular Organization
Mutation in a structural gene that codes for the lysosomal hydrolase that causes disease, called:
TLS Online TPP Program
#Question id: 31152
#Unit 2. Cellular Organization
Incubation of cell extracts with a nonhydrolyzable derivative of GTP for dynamin in the pinching off of vesicles during endocytosis, resulting: