Evidence map›Paper›PMID 31552025›Full record

ArticleFrontiers in immunology2019

Disruption of the preB Cell Receptor Complex Leads to Decreased Bone Mass.

Mohamed Khass, Harunur Rashid, Peter D Burrows, S Louis Bridges, Amjad Javed, Harry W Schroeder

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Beyond resorption: osteoclasts as drivers of bone formation.Cell regeneration (London, England) · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Recent Advances in Osteoclast Biological Behavior.Frontiers in cell and developmental biology · 2021
    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

6 authors at 2 institutions in 2 countries.

Mohamed KhassDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Harunur RashidDepartment of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Peter D BurrowsDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL, United States.
S Louis BridgesDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Amjad JavedDepartment of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, Birmingham, AL, United States.
Harry W SchroederDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
University of Alabama at Birmingham · USNational Water Research Center · EG

Funding

Dental Academic Research Training Program (DART)T90DE022736 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Amjad Javed · 2012 to 2026
$6.7M
Sp7 Mediated Control of Runx2 Function for Osteoblast DifferentiationR01AR062091 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JAVED, AMJAD · 2012 to 2025
$3.4M
Role of VpreB in immunoglobulin antigen binding site selectionR21AI134027 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SCHROEDER, HARRY WILLIAM · 2018 to 2019
$408k
NIAID NIH HHS R21 AI134027NIAMS NIH HHS R01 AR062091NIDCR NIH HHS T90 DE022736
6 · The paper itself

Abstract

In the bone marrow, preB cells are found adjacent to the bone endosteum where bone synthesizing osteoblast and bone resorbing osteoclasts reside. Although there is evidence of interactions between preB and bone cells, the factors that contribute to such interactions are poorly understood. A critical checkpoint for preB cell development assesses the integrity of the nascent immunoglobulin μ heavy chain (HC) by testing whether it can participate in the formation of a preB cell receptor (preBCR), composed of the μ HC and surrogate light chain (LC). In this work, we tested whether loss of preBCR components can affect bone synthesis. A panel of gene targeted mice with sequential blocks in preBCR formation or function [surrogate light chain component lambda 5 deleted (λ5

Indexed as

AnimalsB-LymphocytesBone and BonesFemurHomeostasisImmunoglobulin Heavy ChainsImmunoglobulin Light Chains, SurrogateImmunoglobulin mu-ChainsMice, Inbred C57BLMice, KnockoutOsteoblastsOsteoclastsPre-B Cell ReceptorsSignal TransductionX-Ray MicrotomographyImmunoglobulin Heavy ChainsImmunoglobulin Light Chains, SurrogateImmunoglobulin mu-ChainsPre-B Cell Receptorsadult bone massB cell signalingbone developmentpreB cell receptorsurrogate light chain

Identifiers

PMID31552025
PMCPMC6736987
OpenAlexW2967952154

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.