Evidence map›Paper›PMID 38481529›Full record

ArticleFrontiers in cell and developmental biology2024

Generation of heterozygous and homozygous NF1 lines from human-induced pluripotent stem cells using CRISPR/Cas9 to investigate bone defects associated with neurofibromatosis type 1.

Annabelle Darle, Thibault Mahiet, Déborah Aubin, Manon Doyen, Lina El Kassar, Béatrice Parfait, Gilles Lemaitre, Christine Baldeschi, Jennifer Allouche, Nathalie Holic

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. 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

10 authors at 6 institutions in 1 country.

Annabelle DarleCentre d'Etude des Cellules Souches, Corbeil-Essonnes, France.
Thibault MahietCentre d'Etude des Cellules Souches, Corbeil-Essonnes, France.
Déborah AubinUniversité Paris-Saclay, Université d'Evry, Corbeil-Essonnes, France.
Manon DoyenUniversité Paris-Saclay, Université d'Evry, Corbeil-Essonnes, France.
Lina El KassarCentre d'Etude des Cellules Souches, Corbeil-Essonnes, France.
Béatrice ParfaitEquipe "Génomique et Epigénétique des Tumeurs Rares", UMR INSERM 1016 & Université Paris Cité, Institut Cochin, Paris, France.
Gilles LemaitreUniversité Paris-Saclay, Université d'Evry, Corbeil-Essonnes, France.
Christine BaldeschiUniversité Paris-Saclay, Université d'Evry, Corbeil-Essonnes, France.
Jennifer Allouche *Université Paris-Saclay, Université d'Evry, Corbeil-Essonnes, France.
Nathalie Holic *Université Paris-Saclay, Université d'Evry, Corbeil-Essonnes, France.
Centre Hospitalier Sud Francilien · FRUniversité d'Évry Val-d'Essonne · FRUniversité Paris-Saclay · FRAssociation Francaise contre les Myopathies · FRHôpital Cochin · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is one of the most common genetic disorders caused by heterozygous germline

Indexed as

CRISPR/Cas9disease modelinggene editinghuman-induced pluripotent stem cellsneurofibromatosis type Iosteogenic differentiation

Identifiers

PMID38481529
PMCPMC10935092
OpenAlexW4392239226

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.