Evidence map›Paper›PMID 30890517›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2019

[Structure and function of B-cell linker and its role in the development of B cell-related diseases].

Bin Xiao, Jiaying Li, Mengsi Zhou, Xiaoqing Li, Xiaoyan Huang, Jianfeng Hang, Zhaohui Sun, Linhai Li

Abstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2019. 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, top 85% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 3 institutions in 1 country.

Bin XiaoDepartment of Laboratory Medicine, General Hospital of Southern Theatre Command of PLA, Guangzhou 510010, China.
Jiaying LiDepartment of Clinical Laboratory, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Mengsi ZhouDepartment of Clinical Laboratory, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Xiaoqing LiDepartment of Laboratory Medicine, General Hospital of Southern Theatre Command of PLA, Guangzhou 510010, China.
Xiaoyan HuangDepartment of Laboratory Medicine, General Hospital of Southern Theatre Command of PLA, Guangzhou 510010, China.
Jianfeng HangDepartment of Laboratory Medicine, General Hospital of Southern Theatre Command of PLA, Guangzhou 510010, China.
Zhaohui SunDepartment of Laboratory Medicine, General Hospital of Southern Theatre Command of PLA, Guangzhou 510010, China.
Linhai LiDepartment of Laboratory Medicine, General Hospital of Southern Theatre Command of PLA, Guangzhou 510010, China.
Third Affiliated Hospital of Southern Medical University · CNNanfang Hospital · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B cell linker (BLNK) is a key linker protein of B cell receptor (BCR) signaling pathway. BLNK participates in the regulation of PLC-γactivity and the activation of Ras pathway through its typical structure and interaction network with other proteins, and is thus widely involved in the regulation of B cell proliferation, differentiation, apoptosis and signal transduction. Furthermore, it is closely related to anaphylactic diseases, multiple sclerosis, chromosomal aneuploidy, aneuglobulinemia, B lymphocytic leukemia and lymphoma. Herein we review the structure and biological function of BLNK and its role in B cell-related diseases. BLNK can cooperate with a series of effective proteins to activate BCR signaling pathway, thereby regulating the development, maturation and function of B cells. The functional mutation of BLNK can destroy the homeostasis of B cells and affect the development and maturation of B cells, which leads to the occurrence of B cell related diseases. A comprehensive understanding of the biological functions of BLNK not only provides insights into the pathogenesis of B cell-related diseases, but also inspires new ideas and helps to find breakthroughs for the treatment of these diseases with BLNK as the therapeutic target.

Indexed as

Adaptor Proteins, Signal TransducingApoptosisB-LymphocytesCell DifferentiationCell ProliferationHumansMutationReceptors, Antigen, B-CellSignal TransductionStructure-Activity RelationshipAdaptor Proteins, Signal TransducingB cell linker proteinReceptors, Antigen, B-CellB-cell linkerB cell receptorB cell-related diseasesdifferentiationsignaling pathway

Identifiers

PMID30890517
PMCPMC6765629
OpenAlexW3025406874

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.