Evidence map›Paper›PMID 32858255›Full record

ReviewBone2020

Phylogeny and chemistry of biological mineral transport.

Paul H Schlesinger, Demetrios T Braddock, Quitterie C Larrouture, Evan C Ray, Vladimir Riazanski, Deborah J Nelson, Irina L Tourkova, Harry C Blair

Open access · greenAbstract readReview
In one paragraph

Review in Bone, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. The Effects ofNutrients · 2023
    Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
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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

8 authors at 6 institutions in 2 countries.

Paul H SchlesingerDept of Cell Biology, Washington University, Saint Louis, MO, United States of America.
Demetrios T BraddockDept. of Pathology, Yale New Haven Hospital, 310 Cedar Street, New Haven, CT, United States of America.
Quitterie C LarroutureNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, Windmill Road, Oxford OX3 7LD, UK.
Evan C RayRenal Electrolyte Division, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, United States of America.
Vladimir RiazanskiDept of Neurobiology, Pharmacology & Physiology, University of Chicago, Chicago, IL, United States of America.
Deborah J NelsonDept of Neurobiology, Pharmacology & Physiology, University of Chicago, Chicago, IL, United States of America.
Irina L TourkovaVeteran's Affairs Medical Center, Pittsburgh PA and Department of Pathology, University of Pittsburgh, Pittsburgh, PA, United States of America.
Harry C BlairVeteran's Affairs Medical Center, Pittsburgh PA and Department of Pathology, University of Pittsburgh, Pittsburgh, PA, United States of America. Electronic address: hcblair@imap.pitt.edu.
University of Chicago · USUniversity of Pittsburgh Medical Center · USNuffield Orthopaedic Centre · GBUniversity of Pittsburgh · USWashington University in St. Louis · USYale New Haven Hospital · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Phagosomal Ion Channels as Therapeutic TargetsR01HL125076 · NHLBI · UNIVERSITY OF CHICAGO · PI NELSON, DEBORAH J. · 2015 to 2022
$5.0M
ROLE OF ION CHANNELS IN MONONUCLEAR PHAGOCYTE ACTIVATIONR01GM036823 · NIGMS · UNIVERSITY OF CHICAGO · PI NELSON, DEBORAH J. · 1986 to 2012
$3.2M
Epithelial Osteoblast Function: The Role of Acid TransportR01AR076146 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BLAIR, HARRY COLBERT, NELSON, DEBORAH J. · 2020 to 2024
$2.6M
Proteolytic activation of ENaC in Proteinuric Kidney DiseaseK08DK110332 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RAY, EVAN CROSS · 2016 to 2021
$903k
ENZYME THERAPY FOR CKD-MBD: BREAKING THE BARRIER OF VASCULAR CALCIFICATIONR01DK121326 · NIDDK · YALE UNIVERSITY · PI BRADDOCK, DEMETRIOS · 2020 to 2022
$680k
Epithelial Osteoblast Function: The Role of Acid TransportR56AR076146 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BLAIR, HARRY COLBERT, NELSON, DEBORAH J. · 2019 to 2019
$652k
Regulation of Osteoblasts by ACTH and VEGFI01BX002490 · VA · VETERANS HEALTH ADMINISTRATION · PI BLAIR, HARRY COLBERT · 2015 to 2025
–
BLRD VA I01 BX002490NCATS NIH HHS UL1 TR001863NHLBI NIH HHS R01 HL125076NIAMS NIH HHS R01 AR076146NIAMS NIH HHS R56 AR076146NIDDK NIH HHS K08 DK110332NIDDK NIH HHS R01 DK121326NIGMS NIH HHS R01 GM036823
6 · The paper itself

Abstract

Three physiologically mineralizing tissues - teeth, cartilage and bone - have critical common elements and important evolutionary relationships. Phylogenetically the most ancient densely mineralized tissue is teeth. In jawless fishes without skeletons, tooth formation included epithelial transport of phosphates, a process echoed later in bone physiology. Cartilage and mineralized cartilage are skeletal elements separate from bone, but with metabolic features common to bone. Cartilage mineralization is coordinated with high expression of tissue nonspecific alkaline phosphatase and PHOSPHO1 to harvest available phosphate esters and support mineralization of collagen secreted locally. Mineralization in true bone results from stochastic nucleation of hydroxyapatite crystals within the cross-linked collagen fibrils. Mineral accumulation in dense collagen is, at least in major part, mediated by amorphous aggregates - often called Posner clusters - of calcium and phosphate that are small enough to diffuse into collagen fibrils. Mineral accumulation in membrane vesicles is widely suggested, but does not correlate with a definitive stage of mineralization. Conversely mineral deposition at non-physiologic sites where calcium and phosphate are adequate has been shown to be regulated in large part by pyrophosphate. All of these elements are present in vertebrate bone metabolism. A key biological element of bone formation is an epithelial-like cellular organization which allows control of phosphate, calcium and pH during mineralization.

Indexed as

Bone and BonesCalcification, PhysiologicMineralsOsteogenesisPhylogenyMineralsAcid transportBone mineralCalcium transportHydroxyapatiteOsteoblastPhosphate transport

Identifiers

PMID32858255
PMCPMC7771281
OpenAlexW3081310975

What Socratic 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 Socratic graph.