Evidence map›Paper›PMID 32646852›Full record

ArticleScience immunology2020

The cytoskeletal regulator HEM1 governs B cell development and prevents autoimmunity.

Elisabeth Salzer, Samaneh Zoghi, Máté G Kiss, Frieda Kage, Christina Rashkova, Stephanie Stahnke, Matthias Haimel, René Platzer, Michael Caldera, Rico Chandra Ardy and 19 more

Open access · greenAbstract readCase Reports
In one paragraph

Article in Science immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 49 citations in OpenAlex.

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  18. WAVE regulatory complex.Current biology : CB · 2021
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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

29 authors at 9 institutions in 4 countries.

Elisabeth SalzerLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0002-8118-4934
Samaneh ZoghiLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0002-9015-4446
Máté G KissCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.ORCID 0000-0002-9215-8328
Frieda KageDivision of Molecular Cell Biology, Zoological Institute, Technische Universität Braunschweig, Braunschweig, Germany.ORCID 0000-0002-9834-3946
Christina RashkovaLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.
Stephanie StahnkeDepartment of Cell Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0001-8321-8539
Matthias HaimelLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0002-0320-0214
René PlatzerInstitute for Hygiene and Applied Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Michael CalderaCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.ORCID 0000-0003-3218-6324
Rico Chandra ArdyLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0003-4975-2177
Birgit HoegerLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0001-7491-9405
Jana BlockLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.
David MedgyesiLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.
Celine SinCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.ORCID 0000-0002-4975-4618
Sepideh ShahkaramiResearch Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Renate KainDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Vahid ZiaeePediatric Rheumatology Research Group, Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-4648-3573
Peter HammerlDepartment of Molecular Biology, University of Salzburg, Salzburg, Austria.
Christoph BockLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0001-6091-3088
Jörg MencheCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.ORCID 0000-0002-1583-6404
Loïc DupréLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0002-7278-6503
Johannes B HuppaInstitute for Hygiene and Applied Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-2634-8198
Michael SixtInstitute of Science and Technology Austria, Klosterneuburg, Austria.
Alexis LomakinLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.ORCID 0000-0002-5346-3426
Klemens RottnerDivision of Molecular Cell Biology, Zoological Institute, Technische Universität Braunschweig, Braunschweig, Germany.ORCID 0000-0003-4244-4198
Christoph J BinderCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Theresia E B StradalDepartment of Cell Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0002-0352-9474
Nima RezaeiResearch Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-3836-1827
Kaan BoztugSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria. kaan.boztug@ccri.at.ORCID 0000-0001-8387-9185
Austrian Academy of Sciences · ATHelmholtz Centre for Infection Research · DEMedical University of Vienna · ATUniversal Scientific Education and Research Network · IRCentre National de la Recherche Scientifique · FRInstitute of Science and Technology Austria · ATLudwig Boltzmann Institute for Rare and Undiagnosed Diseases · ATTehran University of Medical Sciences · IRUniversity of Salzburg · AT

Funding

Austrian Science Fund FWF I 2250European Research Council 820074
6 · The paper itself

Abstract

The WAVE regulatory complex (WRC) is crucial for assembly of the peripheral branched actin network constituting one of the main drivers of eukaryotic cell migration. Here, we uncover an essential role of the hematopoietic-specific WRC component HEM1 for immune cell development. Germline-encoded HEM1 deficiency underlies an inborn error of immunity with systemic autoimmunity, at cellular level marked by WRC destabilization, reduced filamentous actin, and failure to assemble lamellipodia. Hem1

Indexed as

AnimalsAutoimmune DiseasesAutoimmunityB-LymphocytesBone Marrow TransplantationCell LineChildCytoskeletonFemaleHumansInfantMembrane ProteinsMice, Inbred C57BLMice, KnockoutT-LymphocytesMembrane ProteinsNCKAP1L protein, human

Identifiers

PMID32646852
PMCPMC7116756
OpenAlexW3040732440

What OpenQuestion holds

Textmetadata
LicenceTDM
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.