Evidence map›Paper›PMID 26985455›Full record

ArticleACS biomaterials science & engineering2015

Nanogel-Mediated RNAi Against Runx2 and Osx Inhibits Osteogenic Differentiation in Constitutively Active BMPR1A Osteoblasts.

Arun R Shrivats, Michael C McDermott, Molly Klimak, Saadyah E Averick, Haichun Pan, Krzysztof Matyjaszewski, Yuji Mishina, Jeffrey O Hollinger

Open access · greenAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Recent Progress of Polymeric Nanogels for Gene Delivery.Current opinion in colloid & interface science · 2019
    Article
  4. Article
  5. Article
  6. 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

8 authors at 2 institutions in 1 country.

Arun R ShrivatsDepartment of Biomedical Engineering, Carnegie Mellon University, 700 Technology Drive, Pittsburgh, Pennsylvania 15219, United States.
Michael C McDermottDepartment of Biomedical Engineering, Carnegie Mellon University, 700 Technology Drive, Pittsburgh, Pennsylvania 15219, United States.
Molly KlimakDepartment of Biomedical Engineering, Carnegie Mellon University, 700 Technology Drive, Pittsburgh, Pennsylvania 15219, United States.
Saadyah E AverickDepartment of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.
Haichun PanSchool of Dentistry, University of Michigan, 1011 North University Avenue, Ann Arbor, Michigan 48109, United States.
Krzysztof MatyjaszewskiDepartment of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.
Yuji MishinaSchool of Dentistry, University of Michigan, 1011 North University Avenue, Ann Arbor, Michigan 48109, United States.
Jeffrey O HollingerDepartment of Biomedical Engineering, Carnegie Mellon University, 700 Technology Drive, Pittsburgh, Pennsylvania 15219, United States.
Carnegie Mellon University · USUniversity of Michigan–Ann Arbor · US

Funding

Molecular pathogenesis of craniosynostosis caused by enhanced BMP signalingR01DE020843 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MISHINA, YUJI · 2010 to 2019
$4.9M
NIDCR NIH HHS R01 DE020843
6 · The paper itself

Abstract

Trauma-induced heterotopic ossification (HO) and fibrodysplasia ossificans progressiva (FOP) are acquired and genetic variants of pathological bone formation occurring in soft tissues. Conventional treatment modalities target the inflammatory processes preceding bone formation. We investigated the development of a prophylaxis for heterotopic bone formation by addressing the biological basis for HO - dysregulation in the bone morphogenetic protein (BMP) signaling pathway. We previously reported the synthesis of cationic nanogel nanostructured polymers (NSPs) for efficient delivery of short interfering ribonucleic acids (siRNAs) and targeted gene silencing. Results suggested that nanogel:siRNA weight ratios of 1:1 and 5:1 silenced

Indexed as

atom transfer radical polymerizationbone morphogenetic proteinfibrodysplasia ossificans progressivagene deliveryheterotopic ossificationsiRNA

Identifiers

PMID26985455
PMCPMC4790085
OpenAlexW2460130313

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.