Evidence map›Paper›PMID 36343514›Full record

ArticleStem cell research2022

Generation and characterization of a human induced pluripotent stem cell (iPSC) line from a patient with congenital heart disease (CHD).

Hui Lin, Shi-Qiao Ye, Zhao-Hui Xu, Jacqueline S Penaloza, Mona Aljuhani, Tatyana Vetter, Ming-Tao Zhao, Kim L McBride

Open access · goldAbstract 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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, 2 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

8 authors at 2 institutions in 1 country.

Hui LinCenter for Cardiovascular Research and The Heart Center, Nationwide Children's Hospital, Columbus, OH, USA.
Shi-Qiao YeCenter for Cardiovascular Research and The Heart Center, Nationwide Children's Hospital, Columbus, OH, USA.
Zhao-Hui XuCenter for Vaccines and Immunity, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, OH, USA.
Jacqueline S PenalozaComputational Genomics Group, The Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
Mona AljuhaniCenter for Cardiovascular Research and The Heart Center, Nationwide Children's Hospital, Columbus, OH, USA.
Tatyana VetterCenter for Gene Therapy, Nationwide Children's Hospital, Columbus, OH, USA.
Ming-Tao ZhaoCenter for Cardiovascular Research and The Heart Center, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, OH, USA.
Kim L McBrideCenter for Cardiovascular Research and The Heart Center, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, OH, USA. Electronic address: Kim.mcbride@nationwidechildrens.org.
Nationwide Children's Hospital · USThe Ohio State University · US

Funding

An integrated human stem cell model for elucidating NOTCH signaling in myocardial-endocardial interactions in cardiac development and diseaseR01HL155282 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI Mingtao Zhao · 2021 to 2026
$3.2M
Exome sequencing and functional studies in familial CHDR01HL109758 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI GARG, VIDU, MCBRIDE, KIM LEWIS · 2012 to 2015
$2.7M
Dissecting SARS-CoV-2 infection in Down syndrome with congenital heart defects using patient-specific iPSCsR21HL165406 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI ZHAO, MINGTAO · 2022 to 2023
$429k
NHLBI NIH HHS R01 HL109758NHLBI NIH HHS R01 HL155282NHLBI NIH HHS R21 HL165406
6 · The paper itself

Abstract

Epstein-Barr virus (EBV) immortalized lymphoblastoid cell lines (LCLs) are widely used for banking. This bioresource could be leveraged for creating human iPSC lines to model diseases including CHD. We generated an LCL-derived iPSC line (NCHi001-A) from a patient with congenital aortic valve stenosis. NCHi001-A was EBV and transgenes free, exhibited stem cell-like morphology, expressed pluripotency markers, has a normal karyotype, and could be differentiated into cells of three germ layers in vitro. Relationship inference via a microarray-based analysis showed NCHi001-A is identical to the parental cell line. NCHi001-A can be used for disease modeling, drug discovery, and cell therapy development.

Indexed as

Epstein-Barr Virus InfectionsHeart Defects, CongenitalInduced Pluripotent Stem CellsHerpesvirus 4, HumanHumans

Identifiers

PMID36343514
PMCPMC9831069
OpenAlexW4307899380

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.