Evidence map›Paper›PMID 30012595›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Pharmacological reactivation of inactive X-linked

Piotr Przanowski, Urszula Wasko, Zeming Zheng, Jun Yu, Robyn Sherman, Lihua Julie Zhu, Michael J McConnell, Jogender Tushir-Singh, Michael R Green, Sanchita Bhatnagar

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 53 citations in OpenAlex.

  1. Protective role of mirtazapine in adult female Mecp2Journal of neurodevelopmental disorders · 2020
    Trial
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  9. Article
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  12. Article
  13. HeterozygousHeliyon · 2024
    Article
  14. Review
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  16. State-of-the-art therapies for Rett syndrome.Developmental medicine and child neurology · 2023
    Review
  17. Multiplex epigenome editing ofScience translational medicine · 2023
    Article
  18. Review
  19. Review
  20. Review
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

10 authors at 3 institutions in 1 country.

Piotr PrzanowskiDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22908.
Urszula WaskoDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22908.
Zeming ZhengDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22908.
Jun YuDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605.
Robyn ShermanDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22908.
Lihua Julie ZhuDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605.
Michael J McConnellDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22908.
Jogender Tushir-SinghDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22908.
Michael R GreenDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605; sb5fk@virginia.edu michael.green@umassmed.edu.ORCID 0000-0003-3017-3298
Sanchita BhatnagarDepartment of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA 22908; sb5fk@virginia.edu michael.green@umassmed.edu.
University of Virginia · USUniversity of Massachusetts Chan Medical School · USHoward Hughes Medical Institute · US

Funding

TRAINING IN CELL AND MOLECULAR BIOLOGYT32GM008136 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI STUKENBERG, P. TODD · 1985 to 2020
$8.5M
Howard Hughes Medical InstituteNIGMS NIH HHS T32 GM008136
6 · The paper itself

Abstract

Rett syndrome (RTT) is a genetic disorder resulting from a loss-of-function mutation in one copy of the X-linked gene methyl-CpG-binding protein 2 (

Indexed as

Methyl-CpG-Binding Protein 2MutationAnimalsCell LineCerebral CortexHumansMiceMice, KnockoutNeuronsRett SyndromeMECP2 protein, humanMecp2 protein, mouseMethyl-CpG-Binding Protein 2brain neuronsMecp2mouse modelRett syndromeX chromosome reactivation

Identifiers

PMID30012595
PMCPMC6077728
OpenAlexW2884620890

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.