Evidence map›Paper›PMID 10781084›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Plasticity in the organization and sequences of human KIR/ILT gene families.

M J Wilson, M Torkar, A Haude, S Milne, T Jones, D Sheer, S Beck, J Trowsdale

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 246 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
246citing papers in PubMed, 3 pooled it
12.7field-weighted citation impact, top 1% 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

246 citing papers in PubMed, 3 syntheses or guidelines pooled it, 625 citations in OpenAlex.

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  20. TheFrontiers in immunology · 2023
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186 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

M J WilsonImmunology Division, Department of Pathology, Tennis Court Road, Cambridge CB2 1QP, United Kingdom.
M Torkar
A Haude
S Milne
T Jones
D Sheer
S Beck
J Trowsdale
The Honourable Society of Lincoln's Inn · GBWellcome Trust · GB

Funding

Cancer Research UK A3585Wellcome Trust
6 · The paper itself

Abstract

The approximately 1-Mb leukocyte receptor complex at 19q13.4 is a key polymorphic immunoregion containing all of the natural killer-receptor KIR and related ILT genes. When the organization of the leukocyte receptor complex was compared from two haplotypes, the gene content in the KIR region varied dramatically, with framework loci flanking regions of widely variable gene content. The ILT genes were more stable in number except for ILT6, which was present only in one haplotype. Analysis of Alu repeats and comparison of KIR gene sequences, which are over 90% identical, are consistent with a recent origin. KIR genesis was followed by extensive duplication/deletion as well as intergenic sequence exchange, reminiscent of MHC class I genes, which provide KIR ligands.

Indexed as

Chromosomes, Human, Pair 19Multigene FamilyAlu ElementsChromosome MappingDNA PrimersExonsGenetic VariationHaplotypesHumansKiller Cells, NaturalMicrosatellite RepeatsPolymerase Chain ReactionReceptors, ImmunologicReceptors, KIRDNA PrimersReceptors, ImmunologicReceptors, KIR

Identifiers

PMID10781084
PMCPMC18309
OpenAlexW2110036277

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.