Evidence map›Paper›PMID 26158512›Full record

ReviewCell death & disease2015

Multiple sclerosis: getting personal with induced pluripotent stem cells.

A Di Ruscio, F Patti, R S Welner, D G Tenen, G Amabile

Erratum issuedOpen access · goldAbstract readReview
In one paragraph

Review in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Frontiers in cell and developmental biology · 2020
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

A Di Ruscio1] Department of Medicine, Harvard Medical School, Boston, MA, USA [2] Harvard Stem Cell Institute, Cambridge, MA, USA.
F PattiMultiple Sclerosis Centre, University of Catania, Catania, Italy.
R S Welner1] Department of Medicine, Harvard Medical School, Boston, MA, USA [2] Harvard Stem Cell Institute, Cambridge, MA, USA.
D G Tenen1] Department of Medicine, Harvard Medical School, Boston, MA, USA [2] Harvard Stem Cell Institute, Cambridge, MA, USA [3] Cancer Science Institute, National University of Singapore, Singapore, Singapore.
G Amabile1] Department of Medicine, Harvard Medical School, Boston, MA, USA [2] Harvard Stem Cell Institute, Cambridge, MA, USA [3] Research and Development, ADIENNE, Lugano, Switzerland.
Harvard University · USHarvard Stem Cell Institute · USUniversity of Catania · IT

Funding

Transcriptional and epigenetic heterogeneity of stem/progenitor cellsP01HL131477 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI David T Scadden · 2017 to 2026
$24.6M
Mechanisms of regulation by RNA in acute myeloid leukemiaR35CA197697 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TENEN, DANIEL G · 2015 to 2021
$7.1M
NCI NIH HHS R35 CA197697NHLBI NIH HHS P01 HL131477
6 · The paper itself

Abstract

Human induced pluripotent stem (iPS) cells can be derived from lineage-restricted cells and represent an important tool to develop novel patient-specific cell therapies and research models for inherited and acquired diseases. Recently, patient-derived iPS cells, containing donor genetic background, have offered a breakthrough approach to study human genetics of neurodegenerative diseases. By offering an unlimited source of patient-specific disease-relevant cells, iPS cells hold great promise for understanding disease mechanisms, identifying molecular targets and developing phenotypic screens for drug discovery. This review will discuss the potential impact of using iPS cell-derived models in multiple sclerosis (MS) research and highlight some of the current challenges and prospective for generating novel therapeutic treatments for MS patients.

Indexed as

Cell- and Tissue-Based TherapyInduced Pluripotent Stem CellsCell DifferentiationCell LineageHumansMultiple SclerosisPrecision Medicine

Identifiers

PMID26158512
PMCPMC4650727
OpenAlexW851476471

What OpenQuestion holds

Textmetadata
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.