Evidence map›Paper›PMID 25053480›Full record

ReviewMethods in molecular biology (Clifton, N.J.)2014

Overview of genetic tools and techniques to study Notch signaling in mice.

Thomas Gridley, Andrew K Groves

Abstract readReview
In one paragraph

Review in Methods in molecular biology (Clifton, N.J.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Recent advances inFrontiers in cell and developmental biology · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

2 authors at 2 institutions in 1 country.

Thomas GridleyCenter for Molecular Medicine, Maine Medical Center Research Institute, 81 Research Drive, Scarborough, ME, 04074, USA, gridlt@mmc.org.
Andrew K Groves
Baylor College of Medicine · USMaine Medical Center · US

Funding

Genetic Regulation of Cochlear DevelopmentR01DC006185 · NIDCD · HOUSE RESEARCH INSTITUTE · PI GROVES, ANDREW K · 2003 to 2014
$3.6M
NIDCD NIH HHS R01 DC006185
6 · The paper itself

Abstract

Aberrations of Notch signaling in humans cause both congenital and acquired defects and cancers. Genetically engineered mice provide the most efficient and cost-effective models to study Notch signaling in a mammalian system. Here, we review the various types of genetic models, tools, and strategies to study Notch signaling in mice, and provide examples of their use. We also provide advice on breeding strategies for conditional mutant mice, and a protocol for tamoxifen administration to mouse strains expressing inducible Cre recombinase-estrogen receptor fusion proteins.

Indexed as

Genetic TechniquesAnimalsBreedingIntegrasesMiceMutationReceptors, NotchRecombinant Fusion ProteinsSignal TransductionTamoxifenCre recombinaseIntegrasesReceptors, NotchRecombinant Fusion ProteinsTamoxifen

Identifiers

PMID25053480
PMCPMC4591040
OpenAlexW2407063622

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.