Evidence map›Paper›PMID 28230927›Full record

ReviewJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2017

CRISPR/CAS9 Technologies.

Bart O Williams, Matthew L Warman

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. In vivo adenine base editing rescues adrenoleukodystrophy in a humanized mouse model.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  4. Review
  5. Current methods for diagnosis of human coronaviruses: pros and cons.Analytical and bioanalytical chemistry · 2021
    Review
  6. Generation and Characterization of Mouse Models for Skeletal Disease.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. An update on the tools for creating transgenic animal models of human diseases - focus on atherosclerosis.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Review
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 2 institutions in 2 countries.

Bart O WilliamsCenter for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, MI, USA.
Matthew L WarmanOrthopaedic Research Laboratories, Boston Children's Hospital, Boston, MA, USA.
Boston Children's Hospital · USVan Andel Institute · US

Funding

Lrp5 signaling in bone mechanotransduction and metabolismR01AR053237 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI ALEXANDER G ROBLING, Matthew L Warman · 2005 to 2026
$9.4M
Analyzing the Role of Wnt Signaling in Bone DevelopmentR01AR053293 · NIAMS · VAN ANDEL RESEARCH INSTITUTE · PI WILLIAMS, BART O · 2007 to 2016
$4.0M
Non-heritable genetic diseases of the skeletal system: Pathogenesis and TreatmentR01AR064231 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI WARMAN, MATTHEW L · 2014 to 2018
$1.9M
Generation and Initial Characterization of Osteocalcin-Deficient RatsR21AR068668 · NIAMS · VAN ANDEL RESEARCH INSTITUTE · PI WILLIAMS, BART O · 2015 to 2016
$460k
Does increasing bone mass also increase bone strength in mouse models of OI?R21AR062326 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI WARMAN, MATTHEW L · 2011 to 2012
$437k
Lrp5 and Lrp6 signaling in bone mechanotransduction and metabolismR56AR053237 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ROBLING, ALEXANDER G, WARMAN, MATTHEW L · 2023 to 2023
$349k
NIAMS NIH HHS R01 AR053237NIAMS NIH HHS R01 AR053293NIAMS NIH HHS R01 AR064231NIAMS NIH HHS R21 AR062326NIAMS NIH HHS R21 AR068668NIAMS NIH HHS R56 AR053237
6 · The paper itself

Abstract

The Clustered Regularly Interspaced Palindromic Repeats (CRISPR)/CRISPR-associated protein (Cas) pathway is revolutionizing biological research. Modifications to this primitive prokaryotic immune system now enable scientists to efficiently edit DNA or modulate gene expression in living eukaryotic cells and organisms. Thus, many laboratories can now perform important experiments that previously were considered scientifically risky or too costly. Here, we describe the components of the CRISPR/Cas system that have been engineered for use in eukaryotes. We also explain how this system can be used to genetically modify cell lines and model organisms, or regulate gene expression in order to search for new participants in biological pathways. © 2017 American Society for Bone and Mineral Research.

Indexed as

CRISPR-Cas SystemsAnimalsGene EditingHumansANIMAL MODELSGENE EDITINGMOLECULAR BIOLOGY

Identifiers

PMID28230927
PMCPMC5413371
OpenAlexW2591055995

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.