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Hemoglobin α in the blood vessel wall.
[alpha-thalassemia]
Hemoglobin
has
been
studied
and
well
characterized
in
red
blood
cells
for
over
100
years
.
However
,
new
work
has
indicated
that
the
hemoglobin
α
subunit
(
Hb
α
)
is
also
found
within
the
blood
vessel
wall
,
where
it
appears
to
localize
at
the
myoendothelial
junction
(
MEJ
)
and
plays
a
role
in
regulating
nitric
oxide
(
NO
)
signaling
between
endothelium
and
smooth
muscle
.
This
discovery
has
created
a
new
paradigm
for
the
control
of
endothelial
nitric
oxide
synthase
activity
,
nitric
oxide
diffusion
,
and
,
ultimately
,
vascular
tone
and
blood
pressure
.
This
review
discusses
the
current
knowledge
of
hemoglobin
׳
s
properties
as
a
gas
exchange
molecule
in
the
bloodstream
and
extrapolates
the
properties
of
Hbα
biology
to
the
MEJ
signaling
domain
.
Specifically
,
we
propose
that
Hb
α
is
present
at
the
MEJ
to
regulate
NO
release
and
diffusion
in
a
restricted
physical
space
,
which
would
have
powerful
implications
for
the
regulation
of
blood
flow
in
peripheral
resistance
arteries
.
Diseases
Validation
Diseases presenting
"blood pressure"
symptom
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
cadasil
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cushing syndrome
fabry disease
familial mediterranean fever
lymphangioleiomyomatosis
pendred syndrome
proteus syndrome
scrub typhus
systemic capillary leak syndrome
thoracic outlet syndrome
typhoid
von hippel-lindau disease
werner syndrome
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