Evidence map›Paper›PMID 29616049›Full record

ReviewFrontiers in immunology2018

Regulation of the Development and Function of B Cells by ZBTB Transcription Factors.

Can Zhu, Ge Chen, Ying Zhao, Xiao-Ming Gao, Jun Wang

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
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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

5 authors at 1 institution in 1 country.

Can ZhuInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Ge ChenInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Ying ZhaoDepartment of Pathophysiology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
Xiao-Ming GaoInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Jun WangInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The large ZBTB family comprises a diverse group of transcriptional factors. Several ZBTB proteins have emerged as critical factors that regulate the lineage commitment, differentiation, and function of lymphoid cells as well as many other developmental events. For instance, dysfunctions of ZBTB20 or ZBTB24 have been linked to multisystem failures in humans. Within the B-cell lineage, BCL6, ZBTB7A, ZBTB17, and ZBTB1 regulate the development/differentiation of B cells in both bone marrow and peripheral lymphoid organs, while ZBTB20 and ZBTB32 seem to mainly impact the maintenance of terminal plasma cells. Given the importance of B cells in the prevention and treatment of infectious or autoimmune disorders, we herein summarize the roles of seven ZBTB family members (BCL6, ZBTB7A, ZBTB17, ZBTB20, ZBTB32, ZBTB1, and ZBTB24) in the development, differentiation, and function of B cells as well as the underlying molecular mechanisms.

Indexed as

Cell DifferentiationZinc FingersAnimalsBiomarkersB-LymphocytesDNA-Binding ProteinsGene Expression RegulationHumansMultigene FamilyTranscription FactorsBiomarkersDNA-Binding ProteinsTranscription FactorsZBTB7A protein, humanB cellsBCL6ZBTB1ZBTB17ZBTB20ZBTB24ZBTB32ZBTB7A

Identifiers

PMID29616049
PMCPMC5869932
OpenAlexW2790377199

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.