Evidence map›Paper›PMID 23241924›Full record

ReviewCalcified tissue international2013

Biomineralization mechanisms: a new paradigm for crystal nucleation in organic matrices.

Arthur Veis, Jason R Dorvee

Abstract readReview
In one paragraph

Review in Calcified tissue international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 160 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. A noveliScience · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Hierarchy of Bioapatites.International journal of molecular sciences · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article
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

2 authors at 1 institution in 1 country.

Arthur VeisDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, 303 E. Chicago Avenue, Chicago, 60611, USA, aveis@northwestern.edu.
Jason R Dorvee
Northwestern University · US

Funding

MATRIX COMPONENT INTERACTIONS IN BONE, DENTIN AND INVERTEBRATE MINERALR01DE001374 · NIDCR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ALVARES, KEITH, STOCK, STUART R · 1985 to 2013
$4.6M
NIDCR NIH HHS R01 DE001374NIDCR NIH HHS R01-DE01374
6 · The paper itself

Abstract

There is substantial practical interest in the mechanism by which the carbonated apatite of bone mineral can be initiated specifically in a matrix. The current literature is replete with studies aimed at mimicking the properties of vertebrate bone, teeth, and other hard tissues by creating organic matrices that can be mineralized in vitro and either functionally substitute for bone on a permanent basis or serve as a temporary structure that can be replaced by normal remodeling processes. A key element in this is mineralization of an implant with the matrix and mineral arranged in the proper orientations and relationships. This review examines the pathway to crystallization from a supersaturated calcium phosphate solution in vitro, focusing on the basic mechanistic questions concerning mineral nucleation and growth. Since bone and dentin mineral forms within collagenous matrices, we consider how the in vitro crystallization mechanisms might or might not be applicable to understanding the in vivo processes of biomineralization in bone and dentin. We propose that the pathway to crystallization from the calcium phosphate-supersaturated tissue fluids involves the formation of a dense liquid phase of first-layer bound-water hydrated calcium and phosphate ions in which the crystallization is nucleated. SIBLING proteins and their in vitro analogs, such as polyaspartic acids, have similar dense liquid first-layer bound-water surfaces which interact with the dense liquid calcium phosphate nucleation clusters and modulate the rate of crystallization within the bone and dentin collagen fibril matrix.

Indexed as

Calcification, PhysiologicCalcinosisAnimalsApatitesBone and BonesBone RemodelingCalciumCalcium PhosphatesCollagenCrystallizationDentinExtracellular MatrixIonsMineralsPeptidesPhosphatesApatitesCalciumcalcium phosphateCalcium PhosphatescarboapatiteCollagenIonsMineralsPeptidesPhosphatespolyaspartatePolymersWater

Identifiers

PMID23241924
PMCPMC3726565
OpenAlexW2019295836

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.