Evidence map›Paper›PMID 40649802›Full record

ArticleInternational journal of molecular sciences2025

Hereditary α-Tryptasemia and Peripheral Blood

Olga Tockova, Tanja Planinsek Rucigaj, Simona Ivancan, Urska Bidovec Stojkovic, Matija Rijavec, Julij Šelb, Peter Korošec

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Olga TockovaDepartment of Dermatovenereology, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Tanja Planinsek RucigajDepartment of Dermatovenereology, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Simona IvancanChildren's Hospital, Department of Hematology and Oncology, University Medical Center Ljubljana, 1000 Ljubljana, Slovenia.
Urska Bidovec StojkovicLaboratory for Clinical Immunology & Molecular Genetics, University Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.ORCID 0000-0001-8978-6887
Matija RijavecLaboratory for Clinical Immunology & Molecular Genetics, University Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.ORCID 0000-0002-2596-4952
Julij ŠelbLaboratory for Clinical Immunology & Molecular Genetics, University Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.
Peter KorošecLaboratory for Clinical Immunology & Molecular Genetics, University Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.

Funding

The Slovenian Research and Innovation Agency P3-0360 and J3-3072
6 · The paper itself

Abstract

Hereditary α-tryptasemia (HαT)-a genetic trait caused by increased α-tryptase-encoding typtase alpha/beta-1 (TPSAB1) copy number-is associated with adult mastocytosis. The primary objective was to assess the association between α-tryptase and pediatric mastocytosis. We also want to evaluate whether the

Indexed as

Mastocytosis, CutaneousMastocytosis, SystemicMutationProto-Oncogene Proteins c-kitTryptasesAdolescentChildChild, PreschoolFemaleGenotypeHumansInfantMaleMast Cell Activation SyndromeProspective StudiesKIT protein, humanProto-Oncogene Proteins c-kitTPSAB1 protein, humanTryptasesbone marrowdiagnosishereditary α-tryptasemiaKIT D816Vmastocytosispediatricsperipheral blood

Identifiers

PMID40649802
PMCPMC12249517

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.