Evidence map›Paper›PMID 35193008›Full record

ArticleStem cell research2022

Generation of three induced pluripotent stem cells lines from patients with esophageal atresia/tracheoesophageal fistula type C.

Suleen Raad, Anu David, Wendy Chung, Christophe Faure

Abstract read
In one paragraph

Article in Stem cell research, 2022. 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
–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

2 citing papers in PubMed.

  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

4 authors.

Suleen RaadEsophageal Development and Engineering Laboratory, Sainte-Justine Research Centre, 3715 Côte Sainte Catherine, H3T1C5, Montreal, QC, Canada.
Anu DavidEsophageal Development and Engineering Laboratory, Sainte-Justine Research Centre, 3715 Côte Sainte Catherine, H3T1C5, Montreal, QC, Canada.
Wendy ChungKennedy Family Professor of Pediatrics and Medicine, Chief, Clinical Genetics Columbia University, 1150 St. Nicholas Avenue, Room 620, New York, NY 10032, USA.
Christophe FaureEsophageal Development and Engineering Laboratory, Sainte-Justine Research Centre, Esophageal Atresia Clinic and Division of Pediatric Gastroenterology Hepatology and Nutrition, CHU Sainte Justine, 3715 Côte Sainte Catherine, Université de Montréal, H3T1C5 Montréal, QC, Canada. Electronic address: christophe.faure@umontreal.ca.

Funding

Project-3: Modeling EA/TEF in human organoidsP01HD093363 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI Wendy K Chung, Paul scot Kingma · 2017 to 2026
$16.2M
NICHD NIH HHS P01 HD093363
6 · The paper itself

Abstract

Esophageal atresia/tracheoesophageal fistula (EA/TEF) is the most common congenital anomaly of the upper gastrointestinal tract affecting 1 in 3,000 which could stem from a developmental anomaly of the foregut. The cause is not fully understood. We generated three iPSC cell lines using peripheral blood mononuclear cells (PBMCs) from EA/TEF type C patients. Pluripotency and trilineage differentiation capacity of these three iPSC cell lines were confirmed by gene and protein expression profiles and the differentiation ability into the three germ layers. The generated disease-specific cell lines could serve as a tool to investigate the mechanisms of EA/TEF and acquired associated diseases.

Indexed as

Esophageal AtresiaInduced Pluripotent Stem CellsTracheoesophageal FistulaHumansLeukocytes, Mononuclear

Identifiers

PMID35193008
PMCPMC10104726

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.