-
Marco Sardiello and co-workers
discovered that the
synthesis of most
lysosomal enzymes and
membrane proteins is
controlled by
transcription factor EB...
-
Lysosomal storage diseases (LSDs; /ˌlaɪsəˈsoʊməl/) are a
group of over 70 rare
inherited metabolic disorders that
result from
defects in
lysosomal function...
-
Lysosomal-****ociated
membrane protein 1 (LAMP-1) also
known as lysosome-****ociated
membrane glycoprotein 1 and CD107a (Cluster of
Differentiation 107a)...
-
Lysosomal acid
lipase deficiency (LAL
deficiency or LAL-D) or
Wolman Disease, is an
autosomal recessive inborn error of
metabolism that
results in the...
-
infusion of a
solution containing the enzyme. ERT is
available for some
lysosomal storage diseases:
Gaucher disease,
Fabry disease, MPS I, MPS II (Hunter...
- in the
central nervous system with its
subcellular location being in
lysosomal membranes. TMEM106B
helps facilitate important functions for maintaining...
-
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...
- to
their destination. It
resides at the
intersection of the secretory,
lysosomal, and
endocytic pathways. It is of
particular importance in processing...
-
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...
-
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...
