-
Ferroportin-1, also
known as
solute carrier family 40
member 1 (SLC40A1) or iron-regulated
transporter 1 (IREG1), is a
protein that in
humans is encoded...
-
Hemochromatosis type 4 is a
hereditary iron
overload disorder that
affects ferroportin, an iron
transport protein needed to
export iron from
cells into circulation...
- mammals,
ferroportin. Hephaestin, a
ferroxidase that can
oxidize Fe2+ to Fe3+ and is
found mainly in the
small intestine,
helps ferroportin transfer iron...
- low, such as in hemochromatosis, iron
overload occurs due to
increased ferroportin mediated iron
efflux from
storage and
increased gut iron absorption....
- the iron
regulatory proteins hemojuvelin,
transferrin receptor-2 and
ferroportin.
Hereditary hemochromatosis is
characterized by an
accelerated rate of...
- and
release from the liver.
Hepcidin production and
release shuts down
ferroportin, a
protein that
controls export of iron from the gut and from iron storing...
-
African people carry a
unique ferroportin mutation that
predisposes them to iron overload,
making it a kind of
ferroportin disease. African-Americans, who...
-
concentrations in
excess of 5 μg Mn/m3 can lead to Mn-induced symptoms.
Increased ferroportin protein expression in
human embryonic kidney (HEK293)
cells is ****ociated...
- mammals,
ferroportin. Hephaestin, a
ferroxidase that can
oxidize Fe2+ to Fe3+ and is
found mainly in the
small intestine,
helps ferroportin transfer iron...
- for
ferroportin,
prove the rule:
these people have
plenty of hepcidin, but
their cells lack the
proper response to it. So, in
people with
ferroportin proteins...
