Evidence map›Paper›PMID 30505649›Full record

ArticleCurrent molecular biology reports2018

IVD Development: Nucleus pulposus development and sclerotome specification.

Bashar Alkhatib, Ga I Ban, Sade Williams, Rosa Serra

Abstract read
In one paragraph

Article in Current molecular biology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

4 authors at 1 institution in 1 country.

Bashar AlkhatibUniversity of Alabama at Birmingham.
Ga I BanUniversity of Alabama at Birmingham.
Sade WilliamsUniversity of Alabama at Birmingham.
Rosa SerraUniversity of Alabama at Birmingham.
University of Alabama at Birmingham · US

Funding

TGF-Beta in the Pathology and Development of the SpineR01AR053860 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SERRA, ROSA A. · 2007 to 2017
$3.2M
Training Program in Rheumatic and Musculoskeletal Diseases ResearchT32AR069516 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI John D Mountz · 2016 to 2026
$2.6M
TGF-beta in the Pathology and Development of the SpineR56AR053860 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SERRA, ROSA A. · 2020 to 2020
$426k
NIAMS NIH HHS R01 AR053860NIAMS NIH HHS R56 AR053860NIAMS NIH HHS T32 AR069516
6 · The paper itself

Abstract

purpose of reviewIntervertebral discs (IVD) are derived from embryonic notochord and sclerotome. The nucleus pulposus is derived from notochord while other connective tissues of the spine are derived from sclerotome. This manuscript will review the past 5 years of research into IVD development. RECENT

findingsOver the past several years, advances in understanding the step-wise process that govern development of the nucleus pulposus and the annulus fibrosus have been made. Generation of tissues from induced or embryonic stem cells into nucleus pulposus and paraxial mesoderm derived tissues has been accomplished SUMMARY: Understanding how the IVD develops will provide the foundation for future repair, regeneration, and tissue engineering strategies for IVD disease.

Indexed as

annulus fibrosusaxial skeleton developmentnotochordnucleus pulposussclerotome

Identifiers

PMID30505649
PMCPMC6261384
OpenAlexW2884969665

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.