-
membrane and
secrete their contents, a
process called lysosomal exocytosis.
After degradation lysosomal products are
transported out of the
lysosome through...
-
Lysosomal storage diseases (LSDs; /ˌlaɪsəˈsoʊməl/) are a
group of over 70 rare
inherited metabolic disorders that
result from
defects in
lysosomal function...
-
disease Type IIb) is a
metabolic disorder.
Danon disease is an X-linked
lysosomal and
glycogen storage disorder ****ociated with
hypertrophic cardiomyopathy...
-
Lysosomal acid
lipase deficiency (LAL
deficiency or LAL-D) or
Wolman Disease, is an
autosomal recessive inborn error of
metabolism that
results in the...
-
Lysosomal-****ociated
membrane protein 1 (LAMP-1) also
known as lysosome-****ociated
membrane glycoprotein 1 and CD107a (Cluster of
Differentiation 107a)...
-
Lysosomal lipase is a form of
lipase which functions intracellularly, in the lysosomes. The
primary function of
lysosomal lipase is to
hydrolyze lipids...
-
infusion of a
solution containing the enzyme. ERT is
available for some
lysosomal storage diseases:
Gaucher disease,
Fabry disease, MPS I, MPS II (Hunter...
-
Lysosomal alpha-glucosidase may
refer to:
Glucan 1,4-a-glucosidase, an
enzyme Acid alpha-glucosidase, an
enzyme This set
index page
lists enzyme articles...
-
lysosomal neuraminidase enzyme which in
humans is
encoded by the NEU1 gene. The
protein SIALIDASE-1
encoded by the NEU-1 gene
encodes the
lysosomal enzyme...
-
disease is the most
common of the
lysosomal storage diseases. It is a form of
sphingolipidosis (a
subgroup of
lysosomal storage diseases), as it involves...
