Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Correct sequence of the A*3001 allele obtained by PCR-SSP typing and automated nucleotide sequencing.

Tissue antigens - 1 Oct 1994

Olerup O, Daniels T, Baxter-Lowe L A

Abstract excerpt

No abstract is available from the source.

Topics

Join the communities discussing this publication.

Base Sequence
Consensus Sequence
Genes, MHC Class I
HLA-A Antigens
Polymerase Chain Reaction
Sequence Alignment
Sequence Analysis, DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Sequence Homology, Nucleic Acid

Source

Identifiers

PMID: 7871528
DOI: 10.1111/j.1399-0039.1994.tb02393.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Correct sequence of the A*3001 allele obtained by PCR-SSP typing and automated nucleotide sequencing.PMID 7871528Read ↗

A PCR-based method for detecting rare genotypes in large samples of individuals.Semantic proximity Read ↗

Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa.Semantic proximity Read ↗

Sequence-based detection of single nucleotide polymorphisms.Semantic proximity Read ↗

Alternative approach for rapid and reliable single-nucleotide polymorphism typing with double restriction mutagenesis primer PCR.Semantic proximity Read ↗

A precaution in the detection of heterozygotes by sequencing: comparison of automated DNA sequencing and PCR-restriction fragment length polymorphism methods.Semantic proximity Read ↗

Non-amplification of an allele of the D8S1179 locus due to a point mutation.Semantic proximity Read ↗

Sanger and Next-Generation Sequencing of AAT.Semantic proximity Read ↗

Allele dropout caused by a non-primer-site SNV affecting PCR amplification--a call for next-generation primer design algorithm.Semantic proximity Read ↗

Analysis of genetic variation by polymerase chain reaction-based nucleotide sequencing.Semantic proximity Read ↗

Improved detection of the T(341)C polymorphism in human N-acetyltransferase (NAT2) gene by using two complementary PCR-RFLP methods: better than automated DNA sequencing for detection of heterozygotes.Semantic proximity Read ↗

An effective method for allele-specific sequencing using restriction enzyme and biotinylation (ASSURE B).Semantic proximity Read ↗

Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.