Evidence map›Paper›PMID 16570139›Full record

ArticleImmunogenetics2006

HLA-E, HLA-F, and HLA-G polymorphism: genomic sequence defines haplotype structure and variation spanning the nonclassical class I genes.

Chul-Woo Pyo, Luke M Williams, Yuki Moore, Hironobu Hyodo, Shuying Sue Li, Lue Ping Zhao, Noriko Sageshima, Akiko Ishitani, Daniel E Geraghty

Abstract read
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In one paragraph

Article in Immunogenetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 61 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Chul-Woo PyoThe Clinical Research Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave., N. Seattle, WA 98109-1024, USA.
Luke M Williams
Yuki Moore
Hironobu Hyodo
Shuying Sue Li
Lue Ping Zhao
Noriko Sageshima
Akiko Ishitani
Daniel E Geraghty
Fred Hutch Cancer Center · USNara Medical University · JP

Funding

TRANSPLANTATION IMMUNOLOGYP01AI033484 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HANSEN, JOHN ANDREW · 1992 to 2013
$13.1M
Polymorphism &Transplantation Biology of Novel MHC lociR01AI049245 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GERAGHTY, DANIEL E · 2000 to 2004
$2.3M
Methods for Correlating SNP Haplotypes with CancerR01CA106320 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ZHAO, LUE PING · 2004 to 2008
$1.9M
NCI NIH HHS CA106320NIAID NIH HHS AI33484NIAID NIH HHS AI49213NIAID NIH HHS AI49245
6 · The paper itself

Abstract

Despite several studies that defined the polymorphism of the nonclassical human leukocyte antigen-E (HLA-E), HLA-F, and HLA-G genes, most polymorphisms thus far examined in correlative studies were derived from the coding sequences of these genes. In addition, some discrepancies and ambiguities in the available data have persisted in current databases. To expand the data available and to resolve some of the discrepant data, we have defined protocols that allow for the amplification of 6 to 7 kb of contiguous genomic sequence for each gene, including all of the coding and intron sequences, approximately 2 kb of 5' flanking promoter sequence, and 1 kb of 3' flanking sequence. Using long-range polymerase chain reaction (PCR) protocols, generating either one or two PCR products depending on the locus, amplified genomic DNA was directly sequenced to completion using a set of about 30 primers over each locus to yield contiguous sequence data from both strands. Using this approach, we sequenced 33 genomic DNAs, from Asian, African American, and Caucasian samples. The results of this analysis confirmed several previously reported coding sequence variants, identified several new allelic variants, and also defined extensive variation in intron and flanking sequences. It was possible to construct haplotype maps and to identify tagging single nucleotide polymorphisms that can be used to detect the composite variation spanning all three genes.

Indexed as

Genetic VariationHaplotypesPolymorphism, GeneticAllelesCell Line, TransformedCell MembraneGenetic LinkageHistocompatibility Antigens Class IHLA AntigensHLA-E AntigensHLA-G AntigensHumansPolymorphism, Single NucleotidePromoter Regions, GeneticHistocompatibility Antigens Class IHLA AntigensHLA-E AntigensHLA-F antigensHLA-G Antigens

Identifiers

PMID16570139
OpenAlexW2059848178

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.