Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 227,199,015 papers from all fields of science
Search
Sign In
Create Free Account
Allele-Specific Oligonucleotide
Known as:
ASO
An oligonucleotide designed to be specific for only one allele of a gene.
National Institutes of Health
Create Alert
Alert
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Analysis of common mitochondrial DNA mutations by allele-specific oligonucleotide and Southern blot hybridization.
Sha Tang
,
Michelle C Halberg
,
Kristen C. Floyd
,
Jing Wang
Methods in molecular biology
2012
Corpus ID: 22176235
Mitochondrial disorders are clinically and genetically heterogeneous. There are a set of recurrent point mutations in the…
Expand
2003
2003
ras oncogene mutations in diethylnitrosamine-induced hepatic tumors in medaka (Oryzias latipes), a teleost fish.
Zi Liu
,
S. Kullman
,
D. Bencic
,
M. Torten
,
D. Hinton
Mutation research
2003
Corpus ID: 31749169
2000
2000
DNA damage promotes mistyping in the allele specific oligonucleotide probing analysis of forensic samples
P. Fattorini
,
Federica Cossutta
,
P. Giulianini
,
P. Edomi
,
C. Previderè
Electrophoresis
2000
Corpus ID: 40039384
Five polymerase chain reaction (PCR) products which could not be reliably typed by allele‐specific oligonucleotide (ASO) probing…
Expand
2000
2000
Fluorescent oligonucleotide ligation technology for identification of ras oncogene mutations
F. Eggerding
Molecular Biotechnology
2000
Corpus ID: 27406269
A mutation detection strategy based on multiplex PCR followed by multiplex allele-specific oligonucleotide probe ligation was…
Expand
Highly Cited
1997
Highly Cited
1997
Direct detection of multiple point mutations in mitochondrial DNA.
L. Wong
,
D. Senadheera
Clinical Chemistry
1997
Corpus ID: 14774127
Mitochondrial defects can be caused by mutations in nuclear or mitochondrial DNA. Large deletion/duplication and point mutations…
Expand
1994
1994
Major Histocompatibility Complex Class‐II Alleles in Primary Biliary Cirrhosis
Li Zhang
,
A. P. Weetman
,
M. Bassendine
,
D. B. G. Oliveira
Scandinavian Journal of Immunology
1994
Corpus ID: 39730138
The major histocompatibility complex (MHC) class‐II alleles at the DRBI, DQBl and DPBl loci were investigated in 40 patients with…
Expand
1994
1994
DNA polymorphisms of human apolipoprotein A‐IV gene: frequency and effects on lipid, lipoprotein and apolipoprotein levels in a French population
M. Zaiou
,
S. Visvikis
,
R. Guéguen
,
H. Parra
,
J. Fruchart
,
G. Siest
Clinical Genetics
1994
Corpus ID: 24617410
Genetic polymorphisms of apolipoprotein (apo) A‐IV have been shown to influence lipoprotein metabolism in some human populations…
Expand
1993
1993
Single-step allele-specific polymerase chain reaction HLA-DQ genotyping using ARMS primers.
J. Picard
Human Immunology
1993
Corpus ID: 4024356
Highly Cited
1990
Highly Cited
1990
Two novel variants of transthyretin identified in Japanese cases with familial amyloidotic polyneuropathy: transthyretin (Glu42 to Gly) and transthyretin (Ser50 to Arg).
S. Ueno
,
T. Uemichi
,
N. Takahashi
,
F. Soga
,
S. Yorifuji
,
S. Tarui
Biochemical and Biophysical Research…
1990
Corpus ID: 24492918
Highly Cited
1989
Highly Cited
1989
A novel ochre mutation in the beta-thalassemia gene of a Thai. Identification by direct cloning of the entire beta-globin gene amplified using polymerase chain reactions.
S. Fucharoen
,
G. Fucharoen
,
P. Fucharoen
,
Y. Fukumaki
Journal of Biological Chemistry
1989
Corpus ID: 25038023
The beta-globin genes from a Thai patient compound heterozygous for beta-thalassemia and HbE disease were investigated. The 3.0…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE