Epidermolysis bullosa is a group of rare medical conditions…

Epidermolysis bullosa is a group of rare medical conditions that cause fragile, blistering skin. Patients with the disease have genetic alterations in one or multiple proteins involved in the formation of the adhesive structures called hemidesomosomes. These include: (select all that apply)

Inclusion-cell (I-cell) disease is a rare genetic disorder c…

Inclusion-cell (I-cell) disease is a rare genetic disorder caused by a mutation in the gene that codes for a phosphotransferase enzyme responsible for adding a phosphate group to mannose residues on specific proteins. Which of the following consequences would directly result from defects in this phosphotransferase enzyme? (Select all that apply.)  

You are given two unlabeled tissue samples, one coming from…

You are given two unlabeled tissue samples, one coming from a patient with metastatic cancer and one from a healthy patient. You are asked to differentiate between both samples, but are only given reagents to measure the expression of two types of genes. Which of the following genes would you choose?