Evidence map›Paper›PMID 30136762›Full record

ArticleDevelopmental neurobiology2018

Development of a Novel FIJI-Based Method to Investigate Neuronal Circuitry in Neonatal Mice.

Jillian Mei-Ling Liu, Summer Rose Fair, Behiye Kaya, Jessica Nabile Zuniga, Hasnaa Rashad Mostafa, Michele Joana Alves, Julie A Stephens, Mikayla Jones, M Tahir Aslan, Catherine Czeisler and 1 more

Open access · greenAbstract read
In one paragraph

Article in Developmental neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 1 institution in 1 country.

Jillian Mei-Ling LiuDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
Summer Rose FairDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
Behiye KayaDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
Jessica Nabile ZunigaDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
Hasnaa Rashad MostafaDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
Michele Joana AlvesDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
Julie A StephensDepartment of Biomedical Informatics, Center for Biostatistics, The Ohio State University College of Medicine, Columbus, Ohio.
Mikayla JonesDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
M Tahir AslanDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
Catherine CzeislerDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.
José Javier OteroDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, Ohio.ORCID 0000-0003-0680-4520
The Ohio State University · US

Funding

Mechanisms of Congenital HypoventilationR01HL132355 · NHLBI · OHIO STATE UNIVERSITY · PI CZEISLER, CATHERINE, OTERO, JOSE JAVIER · 2016 to 2020
$2.5M
NHLBI NIH HHS R01 HL132355NHLBI NIH HHS R01HL132355NHLBI NIH HHS R01HL132355S1NHLBI NIH HHS R01HL132355S2
6 · The paper itself

Abstract

The emergence of systems neuroscience tools requires parallel generation of objective analytical workflows for experimental neuropathology. We developed an objective analytical workflow that we used to determine how specific autonomic neural lineages change during postnatal development. While a wealth of knowledge exists regarding postnatal alterations in respiratory neural function, how these neural circuits change and develop in the weeks following birth remains less clear. In this study, we developed our workflow by combining genetic mouse modeling and quantitative immunofluorescent confocal microscopy and used this to examine the postnatal development of neural circuits derived from the transcription factors NKX2.2 and OLIG3 into three medullary respiratory nuclei. Our automated FIJI-based image analysis workflow rapidly and objectively quantified synaptic puncta in user-defined anatomic regions. Using our objective workflow, we found that the density and estimated total number of Nkx2.2-derived afferents into the pre-Bötzinger Complex significantly decreased with postnatal age during the first three weeks of postnatal life. These data indicate that Nkx2.2-derived structures differentially influence pre-Bötzinger Complex respiratory oscillations at different stages of postnatal development.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsHomeobox Protein Nkx-2.2Medulla OblongataMice, TransgenicNerve NetNeuronsRespirationBasic Helix-Loop-Helix ProteinsHomeobox Protein Nkx-2.2Nkx2-2 protein, mouseOlig3 protein, mouseNkx2.2Olig3postinspiratory complexpre-Bötzinger complexretrotrapezoid nucleus

Identifiers

PMID30136762
PMCPMC6391728
OpenAlexW2888530213

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.