Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q40413269)
Watch
English
Single-tube genotyping without oligonucleotide probes.
scientific article published on January 1999
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
title
Single-tube genotyping without oligonucleotide probes
(English)
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
main subject
genotyping
1 reference
based on heuristic
inferred from title
author name string
S Germer
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
R Higuchi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
publication date
1 January 1999
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
published in
Genome Research
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
volume
9
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
page(s)
72-78
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
cites work
Detection of the hereditary hemochromatosis gene mutation by real-time fluorescence polymerase chain reaction and peptide nucleic acid clamping
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
A homogeneous, ligase-mediated DNA diagnostic test
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Product differentiation by analysis of DNA melting curves during the polymerase chain reaction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
The future of genetic studies of complex human diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Allelic discrimination by nick-translation PCR with fluorogenic probes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Kinetic PCR Analysis: Real-time Monitoring of DNA Amplification Reactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Hyperlipidaemia associated with genetic variation in the apolipoprotein B gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Allele-specific enzymatic amplification of beta-globin genomic DNA for diagnosis of sickle cell anemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
A novel method for detecting point mutations or polymorphisms and its application to population screening for carriers of phenylketonuria
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
HLA-DQ alpha allele and genotype frequencies in various human populations, determined by using enzymatic amplification and oligonucleotide probes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Effects of primer-template mismatches on the polymerase chain reaction: human immunodeficiency virus type 1 model studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
DNA probes: applications of the principles of nucleic acid hybridization
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
22 September 2017
Direct allelic variation scanning of the yeast genome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
17 June 2018
Detection of ras gene mutations in pancreatic juice and peripheral blood of patients with pancreatic adenocarcinoma.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
20 August 2018
The molecular basis of the human serum paraoxonase activity polymorphism.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
20 August 2018
Identification of apolipoprotein B100 polymorphisms that affect low-density lipoprotein metabolism: description of a new approach involving monoclonal antibodies and dynamic light scattering.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310703
retrieved
20 August 2018
A monoclonal antibody (BIP 45) detects Ag(c,g) polymorphism of human apolipoprotein B
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9927486
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Consistency and reproducibility of AmpliType PM results between seven laboratories: field trial results
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9927486
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The use of a genetic map of biallelic markers in linkage studies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9927486
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The Arg192 isoform of paraoxonase with low sarin-hydrolyzing activity is dominant in the Japanese
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9927486
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Integrated amplification and detection of the C677T point mutation in the methylenetetrahydrofolate reductase gene by fluorescence resonance energy transfer and probe melting curves
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9927486
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Spectral genotyping of human alleles
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9927486
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Reading bits of genetic information: methods for single-nucleotide polymorphism analysis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9927486
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
310703
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
PubMed ID
9927486
1 reference
stated in
Europe PubMed Central
PMCID
310703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9927486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit