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membrane and
secrete their contents, a
process called lysosomal exocytosis.
After degradation lysosomal products are
transported out of the
lysosome through...
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Lysosomal storage diseases (LSDs; /ˌlaɪsəˈsoʊməl/) are a
group of over 70 rare
inherited metabolic disorders that
result from
defects in
lysosomal function...
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Lysosomal-****ociated
membrane protein 1 (LAMP-1) also
known as lysosome-****ociated
membrane glycoprotein 1 and CD107a (Cluster of
Differentiation 107a)...
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Lysosomal acid
lipase deficiency (LAL
deficiency or LAL-D) or
Wolman Disease, is an
autosomal recessive inborn error of
metabolism that
results in the...
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infusion of a
solution containing the enzyme. ERT is
available for some
lysosomal storage diseases:
Gaucher disease,
Fabry disease, MPS I, MPS II (Hunter...
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Lysosomal lipase is a form of
lipase which functions intracellularly, in the lysosomes. The
primary function of
lysosomal lipase is to
hydrolyze lipids...
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Lipase A,
lysosomal acid type is a
protein that in
humans is
encoded by the LIPA gene. This gene
encodes lipase A, the
lysosomal acid
lipase (also known...
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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...
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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...
- in the
central nervous system with its
subcellular location being in
lysosomal membranes. TMEM106B
helps facilitate important functions for maintaining...
