Evidence map›Paper›PMID 29940267›Full record

ArticleBone2018

Mice harboring a Hajdu Cheney Syndrome mutation are sensitized to osteoarthritis.

S Zanotti, J Yu, D Bridgewater, J M Wolf, E Canalis

Abstract read
In one paragraph

Article in Bone, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Hajdu-Cheney Syndrome: A Systematic Review of the Literature.International journal of environmental research and public health · 2020
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Osteoarthritis: pathogenic signaling pathways and therapeutic targets.Signal transduction and targeted therapy · 2023
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Notch in skeletal physiology and disease.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2018
    Review
  13. A Notch in the joint that exacerbates osteoarthritis.Nature reviews. Rheumatology · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

S ZanottiDepartment of Orthopaedic Surgery, UConn Health, Farmington, CT 06030, United States of America; Department of Medicine, UConn Health, Farmington, CT 06030, United States of America; UConn Musculoskeletal Institute, UConn Health, Farmington, CT 06030, United States of America.
J YuDepartment of Orthopaedic Surgery, UConn Health, Farmington, CT 06030, United States of America; UConn Musculoskeletal Institute, UConn Health, Farmington, CT 06030, United States of America.
D BridgewaterUConn Musculoskeletal Institute, UConn Health, Farmington, CT 06030, United States of America.
J M WolfDepartment of Orthopaedic Surgery, UConn Health, Farmington, CT 06030, United States of America; UConn Musculoskeletal Institute, UConn Health, Farmington, CT 06030, United States of America.
E CanalisDepartment of Orthopaedic Surgery, UConn Health, Farmington, CT 06030, United States of America; Department of Medicine, UConn Health, Farmington, CT 06030, United States of America; UConn Musculoskeletal Institute, UConn Health, Farmington, CT 06030, United States of America. Electronic address: canalis@uchc.edu.
UConn Health · US

Funding

Mechanisms of Notch Action in BoneR01DK045227 · NIDDK · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CANALIS, ERNESTO · 1991 to 2018
$4.7M
NIDDK NIH HHS R01 DK045227
6 · The paper itself

Abstract

Osteoarthritis is a joint disease characterized by cartilage degradation, altered gene expression and inflammation. NOTCH1 and NOTCH2 receptors and the JAGGED1 ligand regulate chondrocyte biology; however, the contribution of Notch signaling to osteoarthritis is controversial. Hajdu Cheney Syndrome (HCS) is a rare genetic disorder affecting the skeleton and associated with NOTCH2 mutations that lead to NOTCH2 gain-of-function. A murine model of the disease (Notch2

Indexed as

AnimalsCells, CulturedHajdu-Cheney SyndromeMaleMiceMice, 129 StrainMice, Inbred C57BLMice, TransgenicMutationOsteoarthritisReceptor, Notch2Notch2 protein, mouseReceptor, Notch2ChondrocytesHajdu Cheney SyndromeNotch2Osteoarthritis

Identifiers

PMID29940267
PMCPMC6083868
OpenAlexW2809126835

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.