Evidence map›Paper›PMID 28257933›Full record

ArticleStem cell research2017

Genetic ablation of the mammalian sterile-20 like kinase 1 (Mst1) improves cell reprogramming efficiency and increases induced pluripotent stem cell proliferation and survival.

Abigail Robertson, Tamer M A Mohamed, Zeinab El Maadawi, Nicholas Stafford, Thuy Bui, Dae-Sik Lim, Elizabeth J Cartwright, Delvac Oceandy

Open access · goldAbstract read
In one paragraph

Article in Stem cell research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Article
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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 4 institutions in 4 countries.

Abigail RobertsonDivision of Cardiovascular Sciences, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
Tamer M A MohamedDivision of Cardiovascular Sciences, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom; J. David Gladstone Research Institutes, San Francisco, CA, USA; Faculty of Pharmacy, Zagazig University, Egypt.
Zeinab El MaadawiDivision of Cardiovascular Sciences, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom; Department of Histology and Cell Biology, Faculty of Medicine, Cairo University, Egypt.
Nicholas StaffordDivision of Cardiovascular Sciences, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
Thuy BuiDivision of Cardiovascular Sciences, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
Dae-Sik LimDepartment of Biological Sciences, KAIST, Daejon, Republic of Korea.
Elizabeth J CartwrightDivision of Cardiovascular Sciences, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
Delvac OceandyDivision of Cardiovascular Sciences, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom. Electronic address: delvac.oceandy@manchester.ac.uk.
Manchester Academic Health Science Centre · GBCairo University · EGGladstone Institutes · USKorea Advanced Institute of Science and Technology · KR

Funding

British Heart Foundation FS/09/046/28043British Heart Foundation PG/11/23/28801British Heart Foundation PG/13/12/30017
6 · The paper itself

Abstract

Adult fibroblasts can be reprogrammed into induced pluripotent stem cells (iPSC) for use in various applications. However, there are challenges in iPSC generation including low reprogramming efficiency, yield, cell survival and viability. Since the Hippo signalling pathway is a key pathway involved in regulating cell proliferation and survival, we here test whether modification of the Hippo pathway will enhance the efficiency of iPSC generation and improve their survival. The Hippo pathway was modified by genetic ablation of the mammalian sterile-20 like kinase 1 (Mst1), a major component of the pathway. Using adult skin fibroblasts isolated from Mst1 knockout mice (Mst1

Indexed as

Cellular ReprogrammingAnimalsCell LineCell ProliferationCell SurvivalFibroblastsHepatocyte Growth FactorHippo Signaling PathwayInduced Pluripotent Stem CellsMiceMice, KnockoutProtein Serine-Threonine KinasesProto-Oncogene ProteinsSignal TransductionTranscription FactorsHepatocyte Growth Factormacrophage stimulating proteinProtein Serine-Threonine KinasesProto-Oncogene ProteinsTranscription FactorsCell proliferationHippo pathwayiPSCMst1Reprogramming

Identifiers

PMID28257933
PMCPMC5376382
OpenAlexW2592957123

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.