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Marco Sardiello and co-workers
discovered that the
synthesis of most
lysosomal enzymes and
membrane proteins is
controlled by
transcription factor EB...
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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 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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Lysosomal-****ociated
membrane protein 1 (LAMP-1) also
known as lysosome-****ociated
membrane glycoprotein 1 and CD107a (Cluster of
Differentiation 107a)...
-
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 trafficking regulator is a
vesicular transport protein ****ociated with Chédiak–Higashi syndrome. In
melanocytic cells LYST gene
expression may...
-
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...
-
receptors bind
newly synthesized lysosomal hydrolases in the trans-Golgi
network (TGN) and
deliver them to pre-
lysosomal compartments.
There are two different...
-
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...
- disease, also
referred to as
mucolipidosis II (ML II), is part of the
lysosomal storage disease family and
results from a
defective phosphotransferase...
