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Molecular diagnosis of α-thalassemias by the colorimetric nanogold.
[alpha-thalassemia]
A
new
application
of
gold
nanoparticles
(
AuNPs
)
as
a
colorimetric
method
for
gene
detection
of
α-thalassemia
Â
1
(
SEA
deletion
)
is
reported
here
for
the
first
time
.
This
technique
is
based
on
color
changes
from
salt
-induced
aggregation
of
un-hybridized
nanogold
probes
after
hybridization
with
the
target
DNA
.
Specific
DNA
probes
were
synthesized
,
thiol
modified
and
conjugated
on
the
surface
of
AuNPs
.
The
target
DNA
was
amplified
and
hybridized
with
the
AuNPs-immobilized
probe
.
Salt
solution
(
NaCl
)
was
added
to
induce
aggregation
of
the
un-hybridized
nanogold
probes
.
The
color
changes
were
visualized
either
by
the
naked
eye
or
by
UV-vis
spectrophotometry
at
520
nm
.
By
this
nanogold
colorimetric
method
samples
carrying
normal
α-globin
genes
could
be
successfully
identified
from
samples
carrying
α-globin
genes
causing
α-thalassemia
Â
1
(
SEA
deletion
)
,
either
as
a
carrier
or
disease
form
.
Results
demonstrated
that
the
new
colorimetric
nanogold
method
is
a
definite
gene
diagnosis
of
α-thalassemia
.
It
is
accurate
,
simple
,
rapid
,
specific
,
sensitive
,
and
cost
effective
.
It
is
also
a
promising
point-of-care
testing
(
POCT
)
method
for
thalassemias
and
other
genetic
disorders
.
The
new
colorimetric
nanogold
is
a
method
of
choice
for
areas
where
access
to
sophisticated
molecular
diagnosis
is
limited
.
Diseases
Validation
Diseases presenting
"first time"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
congenital adrenal hyperplasia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
gm1 gangliosidosis
harlequin ichthyosis
heparin-induced thrombocytopenia
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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