-
Hexosaminidase (EC 3.2.1.52, β-acetylaminodeoxyhexosidase, N-acetyl-β-D-
hexosaminidase, N-acetyl-β-
hexosaminidase, N-acetyl
hexosaminidase, β-hexosaminidase...
-
disorder caused by the
inherited deficiency to
create functional beta-
hexosaminidases A and B.
These catabolic enzymes are
needed to
degrade the neuronal...
-
diagnosed by an ****ay of
hexosaminidase A activity. The
further development of
enzyme ****ays
demonstrated that
levels of
hexosaminidases A and B
could be measured...
- C.
perfringens encodes for
eight hexosaminidases that
break down
hexosamines in the mucus.
These hexosaminidases belong to four
glycoside hydrolase...
-
Heterotaxy with
polysplenia or
asplenia Heterotaxy, visceral, X-linked
Hexosaminidases A and B
deficiency HHH
syndrome Hibernian fever,
familial Hiccups Hidradenitis...
- are 3
forms of beta-
hexosaminidase:
hexosaminidase A is a trimer, with one alpha, one beta-A and one beta-B chain;
hexosaminidase B is a
tetramer of two...
-
Hexosaminidase A (alpha polypeptide), also
known as HEXA, is an
enzyme that in
humans is
encoded by the HEXA gene,
located on the 15th chromosome. Hexosaminidase...
-
insufficiency is Tay–Sachs disease, in
which patients lack the
enzyme hexosaminidase. One
example of
enzyme deficiency is the most
common type of phenylketonuria...
-
genetic disorders that
result from a
deficiency of the
enzyme beta-
hexosaminidase. This
enzyme catalyzes the
biodegradation of
fatty acid derivatives...
- In 2011,
researchers discovered that
pyrimethamine can
increase β-
hexosaminidase activity, thus
potentially slowing down the
progression of late-onset...
