Evidence map›Paper›PMID 39134861›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Live Imaging Analysis of Axonal Regeneration in Human iPSC-Derived Motor Neurons Using a Microfluidic System.

Katherine L Marshall, Mohamed H Farah

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Katherine L MarshallDepartment of Neurology, Neuromuscular Division, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Mohamed H FarahDepartment of Neurology, Neuromuscular Division, Johns Hopkins University School of Medicine, Baltimore, MD, USA. mfarah2@jhmi.edu.

Funding

Axonal pathogenesis of human iPSC-derived motor neuronsR21NS130900 · NINDS · JOHNS HOPKINS UNIVERSITY · PI FARAH, MOHAMED H · 2022 to 2022
$450k
NINDS NIH HHS R21 NS130900
6 · The paper itself

Abstract

Axonal damage is a common feature of traumatic injury and neurodegenerative disease. The capacity for axons to regenerate and to recover functionality after injury is a phenomenon that is seen readily in the peripheral nervous system, especially in rodent models, but human axonal regeneration is limited and does not lead to full functional recovery. Here we describe a system where dynamics of human axonal outgrowth and regeneration can be evaluated via live imaging of human-induced pluripotent stem cell (hiPSC)-derived neurons cultured in microfluidic systems, in which cell bodies are isolated from their axons. This system could aid in studying axonal outgrowth dynamics and could be useful for testing potential drugs that encourage regeneration and repair of the nervous system.

Indexed as

AxonsInduced Pluripotent Stem CellsMotor NeuronsNerve RegenerationCell Culture TechniquesCell DifferentiationCells, CulturedHumansLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesMicrofluidicsAxonal regenerationAxotomyHuman iPSCsLive imagingMicrofluidic devicesMotor neuronsNeuronal cytoskeletal markersOutgrowth

Identifiers

What OpenQuestion holds

Textmetadata
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.