Evidence map›Paper›PMID 37759711›Full record

ReviewBiomolecules2023

The Past, Present, and Future of Genetically Engineered Mouse Models for Skeletal Biology.

Megan N Michalski, Bart O Williams

Abstract readReview
In one paragraph

Review in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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.

Megan N MichalskiDepartment of Cell Biology, Van Andel Institute, Grand Rapids, MI 49503, USA.ORCID 0000-0003-2253-3919
Bart O WilliamsDepartment of Cell Biology, Van Andel Institute, Grand Rapids, MI 49503, USA.

Funding

Deciphering the Role of Frizzled Receptors in Palatal DevelopmentK08DE031039 · NIDCR · VAN ANDEL RESEARCH INSTITUTE · PI MICHALSKI, MEGAN · 2021 to 2025
$546k
NIDCR NIH HHS K08 DE031039
6 · The paper itself

Abstract

The ability to create genetically engineered mouse models (GEMMs) has exponentially increased our understanding of many areas of biology. Musculoskeletal biology is no exception. In this review, we will first discuss the historical development of GEMMs and how these developments have influenced musculoskeletal disease research. This review will also update our 2008 review that appeared in BONEKey, a journal that is no longer readily available online. We will first review the historical development of GEMMs in general, followed by a particular emphasis on the ability to perform tissue-specific (conditional) knockouts focusing on musculoskeletal tissues. We will then discuss how the development of CRISPR/Cas-based technologies during the last decade has revolutionized the generation of GEMMs.

Indexed as

Musculoskeletal DiseasesAnimalsBiologyMicebonecartilagechondrocytecre recombinaseCRISPRi-GONADosteoblastosteoclastosteocytetransgenic mouse

Identifiers

PMID37759711
PMCPMC10526739

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.