"Gaucher's Disease: From Diagnosis to Treatment" was designed as an educational resource for all professionals involved in the care of patients with Gaucher disease (GD). Chapter 1 is an introduction about GD. GD is the most common autosomal recessive lysosomal storage disease (LSD) due to the deficiency or absence of the activity of enzyme glucosylceramidase (GCase) or also known as acidic- glucosidase (GBA1) or uridine phosphate glucosylceramide synthase (UDP-GLC). Defects in these enzymes cause miss-sorting or loss function of lysosomal proteins leading to accumulation of glucocerebroside...

"Caspase 3: Structure, Functions and Interactions" is a book designed as an educational resource for researchers and health care providers who want to learn more about caspase 3. Physicians, pharmacists, other health care professionals can benefit from learning about the function of caspase 3 and its role in diseases and possible treatment options of using caspase 3-like compounds. New or seasoned scientists with research interests in caspases can learn novel ideas or interventions using caspase 3. Caspases are a family of enzymes that play an important role in developing normal organ...