Evidence map›Paper›PMID 36283941›Full record

ArticleUltrasound in medicine & biology2023

Longitudinal in Utero Analysis of Engrailed-1 Knockout Mouse Embryonic Phenotypes Using High-Frequency Ultrasound.

Orlando Aristizábal, Ziming Qiu, Estefania Gallego, Matias Aristizábal, Jonathan Mamou, Yao Wang, Jeffrey A Ketterling, Daniel H Turnbull

Open access · greenAbstract read
In one paragraph

Article in Ultrasound in medicine & biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

8 authors at 3 institutions in 1 country.

Orlando AristizábalSkirball Institute of Biomolecular Medicine and Department of Radiology, New York University Grossman School of Medicine, New York, New York, USA.
Ziming QiuDepartment of Electrical and Computer Engineering, New York University Tandon School of Engineering, New York, New York, USA.
Estefania GallegoSkirball Institute of Biomolecular Medicine and Department of Radiology, New York University Grossman School of Medicine, New York, New York, USA.
Matias AristizábalSkirball Institute of Biomolecular Medicine and Department of Radiology, New York University Grossman School of Medicine, New York, New York, USA.
Jonathan MamouDepartment of Radiology, Weill Cornell Medicine, New York, New York, USA.
Yao WangDepartment of Electrical and Computer Engineering, New York University Tandon School of Engineering, New York, New York, USA.
Jeffrey A KetterlingDepartment of Radiology, Weill Cornell Medicine, New York, New York, USA. Electronic address: jek4011@med.cornell.edu.
Daniel H TurnbullSkirball Institute of Biomolecular Medicine and Department of Radiology, New York University Grossman School of Medicine, New York, New York, USA. Electronic address: daniel.turnbull@med.nyu.edu.
New York University · USCornell University · USWeill Cornell Medicine · US

Funding

In utero mouse embryo phenotyping with high-frequency ultrasoundR01EB022950 · NIBIB · RIVERSIDE RESEARCH INSTITUTE · PI KETTERLING, JEFFREY, TURNBULL, DANIEL H · 2016 to 2019
$2.8M
NIBIB NIH HHS R01 EB022950
6 · The paper itself

Abstract

Large-scale international efforts to generate and analyze loss-of-function mutations in each of the approximately 20,000 protein-encoding gene mutations are ongoing using the "knockout" mouse as a model organism. Because one-third of gene knockouts are expected to result in embryonic lethality, it is important to develop non-invasive in utero imaging methods to detect and monitor mutant phenotypes in mouse embryos. We describe the utility of 3-D high-frequency (40-MHz) ultrasound (HFU) for longitudinal in utero imaging of mouse embryos between embryonic days (E) 11.5 and E14.5, which represent critical stages of brain and organ development. Engrailed-1 knockout (En1-ko) mouse embryos and their normal control littermates were imaged with HFU in 3-D, enabling visualization of morphological phenotypes in the developing brains, limbs and heads of the En1-ko embryos. Recently developed deep learning approaches were used to automatically segment the embryonic brain ventricles and bodies from the 3-D HFU images, allowing quantitative volumetric analyses of the En1-ko brain phenotypes. Taken together, these results show great promise for the application of longitudinal 3-D HFU to analyze knockout mouse embryos in utero.

Indexed as

BrainImaging, Three-DimensionalAnimalsEmbryo, MammalianMiceMice, KnockoutPhenotypeUltrasonographyIn utero imagingLongitudinal 3-D ultrasoundMouse embryoMutant phenotype analysis

Identifiers

PMID36283941
PMCPMC9712241
OpenAlexW4307140684

What OpenQuestion holds

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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.