Evidence map›Paper›PMID 38003351›Full record

ArticleInternational journal of molecular sciences2023

CRISPR/Cas9 Directed Reprogramming of iPSC for Accelerated Motor Neuron Differentiation Leads to Dysregulation of Neuronal Fate Patterning and Function.

Katie Davis-Anderson, Sofiya Micheva-Viteva, Emilia Solomon, Blake Hovde, Elisa Cirigliano, Jennifer Harris, Scott Twary, Rashi Iyer

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  3. Review
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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 2 institutions in 2 countries.

Katie Davis-AndersonBioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87544, USA.ORCID 0000-0003-0549-2844
Sofiya Micheva-VitevaBioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87544, USA.ORCID 0000-0002-2693-4333
Emilia SolomonBioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87544, USA.
Blake HovdeBioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87544, USA.ORCID 0000-0002-7112-3310
Elisa CiriglianoDepartment of Psychology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Jennifer HarrisInformation Systems and Modeling Division, Los Alamos National Laboratory, Los Alamos, NM 87544, USA.ORCID 0000-0001-7406-1904
Scott TwaryBioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87544, USA.
Rashi IyerPhysical Chemistry and Applied Spectroscopy, Los Alamos National Laboratory, Los Alamos, NM 87544, USA.
Los Alamos National Laboratory · USUniversity of British Columbia · CA

Funding

Defence Threat Reduction Agency DTRA-JSTO HDTRA1-1-38382Los Alamos National Security (United States) 20190167DR
6 · The paper itself

Abstract

Neurodegeneration causes a significant disease burden and there are few therapeutic interventions available for reversing or slowing the disease progression. Induced pluripotent stem cells (iPSCs) hold significant potential since they are sourced from adult tissue and have the capacity to be differentiated into numerous cell lineages, including motor neurons. This differentiation process traditionally relies on cell lineage patterning factors to be supplied in the differentiation media. Genetic engineering of iPSC with the introduction of recombinant master regulators of motor neuron (MN) differentiation has the potential to shorten and streamline cell developmental programs. We have established stable iPSC cell lines with transient induction of exogenous

Indexed as

Induced Pluripotent Stem CellsCell DifferentiationCRISPR-Cas SystemsMotor NeuronsNeurogenesisCRISPR/Cas9 gene editingelectrophysiological activityglobal transcriptomeiPSC reprogrammingmotor neuron development

Identifiers

PMID38003351
PMCPMC10671572
OpenAlexW4388569053

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.