Evidence map›Paper›PMID 31683583›Full record

ArticleInternational journal of molecular sciences2019

Generation of Mouse Parthenogenetic Epiblast Stem Cells and Their Imprinting Patterns.

Bong Jong Seo, Hyun Sik Jang, Hyuk Song, Chankyu Park, Kwonho Hong, Jeong Woong Lee, Jeong Tae Do

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Derivation of Mouse Parthenogenetic Advanced Stem Cells.International journal of molecular sciences · 2021
    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

7 authors.

Bong Jong SeoDepartment of Stem Cell and Regenerative Biotechnology, Konkuk Institute of Technology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Korea. bjseo@konkuk.ac.kr.
Hyun Sik JangDepartment of Stem Cell and Regenerative Biotechnology, Konkuk Institute of Technology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Korea. arctrus@konkuk.ac.kr.
Hyuk SongDepartment of Stem Cell and Regenerative Biotechnology, Konkuk Institute of Technology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Korea. songh@konkuk.ac.kr.
Chankyu ParkDepartment of Stem Cell and Regenerative Biotechnology, Konkuk Institute of Technology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Korea. chankyu@konkuk.ac.kr.
Kwonho HongDepartment of Stem Cell and Regenerative Biotechnology, Konkuk Institute of Technology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Korea. hongk@konkuk.ac.kr.
Jeong Woong LeeResearch Center of Integrative Cellulomics, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Korea. jwlee@kribb.re.kr.ORCID 0000-0002-2649-9677
Jeong Tae DoDepartment of Stem Cell and Regenerative Biotechnology, Konkuk Institute of Technology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Korea. dojt@konkuk.ac.kr.ORCID 0000-0001-6721-1441

Funding

National Research Foundation of Korea 2015R15A1009701National Research Foundation of Korea 2016M3A9B6946835
6 · The paper itself

Abstract

Pluripotent stem cells can be established from parthenogenetic embryos, which only possess maternal alleles with maternal-specific imprinting patterns. Previously, we and others showed that parthenogenetic embryonic stem cells (pESCs) and parthenogenetic induced pluripotent stem cells (piPSCs) progressively lose the bimaternal imprinting patterns. As ESCs and iPSCs are naïve pluripotent stem cells, parthenogenetic primed pluripotent stem cells have not yet been established, and thus, their imprinting patterns have not been studied. Here, we first established parthenogenetic epiblast stem cells (pEpiSCs) from 7.5 dpc parthenogenetic implantation embryos and compared the expression patterns and DNA methylation status of the representative imprinted genes with biparental EpiSCs. We found that there were no striking differences between pEpiSCs and biparental EpiSCs with respect to morphology, pluripotency gene expression, and differentiation potential, but there were differences in the expression and DNA methylation status of imprinted genes (

Indexed as

AnimalsCell DifferentiationCells, CulturedDNA MethylationEmbryonic Stem CellsFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalGenomic ImprintingGerm LayersInduced Pluripotent Stem CellsInsulin-Like Growth Factor IIMiceParthenogenesisPluripotent Stem CellsRNA, Long NoncodingH19 long non-coding RNAInsulin-Like Growth Factor IIRNA, Long Noncodingembryonic stem cell (ESC)epiblast stem cell (EpiSC)imprinted geneparthenogenesis

Identifiers

PMID31683583
PMCPMC6862121

What OpenQuestion holds

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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.