Evidence map›Paper›PMID 32109236›Full record

ArticleScientific reports2020

Generation of human androgenetic induced pluripotent stem cells.

Na Young Choi, Jin Seok Bang, Yo Seph Park, Minseong Lee, Han Sung Hwang, Kisung Ko, Soon Chul Myung, Natalia Tapia, Hans R Schöler, Gwang Jun Kim and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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 41% 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

11 authors at 5 institutions in 3 countries.

Na Young ChoiDepartment of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, 05029, Republic of Korea.
Jin Seok BangDepartment of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, 05029, Republic of Korea.
Yo Seph ParkDepartment of Stem Cell Research, TJC Life Research and Development Center, TJC Life, Seoul, 06698, Republic of Korea.
Minseong LeeDepartment of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, 05029, Republic of Korea.
Han Sung HwangDepartment of Obstetrics and Gynecology, Research Institute of Medical Science, Konkuk University School of Medicine, Seoul, 05030, Republic of Korea.
Kisung KoDepartment of Medicine, College of Medicine, Chung-Ang University, Seoul, 06974, Republic of Korea.
Soon Chul MyungDepartment of Urology, Chung-Ang University College of Medicine, Seoul, 06974, Republic of Korea.
Natalia TapiaInstitute of Biomedicine of Valencia, Spanish National Research Council, Jaime Roig 11, 46010, Valencia, Spain.ORCID http://orcid.org/0000-0003-0226-1952
Hans R SchölerDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, 48149, Münster, Germany.ORCID http://orcid.org/0000-0003-2643-5136
Gwang Jun KimDepartment of Obstetrics and Gynecology, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, 06974, Republic of Korea.
Kinarm KoDepartment of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, 05029, Republic of Korea. knko@kku.ac.kr.
Konkuk University · KRChung-Ang University · KRChung-Ang University Hospital · KRInstituto de Biomedicina de Valencia · ESUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In humans, parthenogenesis and androgenesis occur naturally in mature cystic ovarian teratomas and androgenetic complete hydatidiform moles (CHM), respectively. Our previous study has reported human parthenogenetic induced pluripotent stem cells from ovarian teratoma-derived fibroblasts and screening of imprinted genes using genome-wide DNA methylation analysis. However, due to the lack of the counterparts of uniparental cells, identification of new imprinted differentially methylated regions has been limited. CHM are inherited from only the paternal genome. In this study, we generated human androgenetic induced pluripotent stem cells (AgHiPSCs) from primary androgenetic fibroblasts derived from CHM. To investigate the pluripotency state of AgHiPSCs, we analyzed their cellular and molecular characteristics. We tested the DNA methylation status of imprinted genes using bisulfite sequencing and demonstrated the androgenetic identity of AgHiPSCs. AgHiPSCs might be an attractive alternative source of human androgenetic embryonic stem cells. Furthermore, AgHiPSCs can be used in regenerative medicine, for analysis of genomic imprinting, to study imprinting-related development, and for disease modeling in humans.

Indexed as

Paternal InheritanceCell DifferentiationCells, CulturedDNA MethylationFemaleFibroblastsGenomic ImprintingHumansHydatidiform MoleInduced Pluripotent Stem CellsMalePregnancyReproduction, Asexual

Identifiers

PMID32109236
PMCPMC7046633
OpenAlexW3010608348

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.