Evidence map›Paper›PMID 32759720›Full record

ArticleInternational journal of molecular sciences2020

Membrane Repair Deficit in Facioscapulohumeral Muscular Dystrophy.

Adam J Bittel, Sen Chandra Sreetama, Daniel C Bittel, Adam Horn, James S Novak, Toshifumi Yokota, Aiping Zhang, Rika Maruyama, Kenji Rowel Q Lim, Jyoti K Jaiswal and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Molecular therapy. Nucleic acids · 2026
    Article
  5. Article
  6. IncreasedInternational journal of molecular sciences · 2025
    Article
  7. Article
  8. Muscular Dystrophies.Advances in experimental medicine and biology · 2025
    Review
  9. Article
  10. Article
  11. Molecular and Phenotypic Changes in FLExDUX4 Mice.Journal of personalized medicine · 2023
    Article
  12. Influence ofInternational journal of molecular sciences · 2023
    Review
  13. Article
  14. Current Strategies of Muscular Dystrophy Therapeutics: An Overview.Methods in molecular biology (Clifton, N.J.) · 2023
    Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  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

11 authors at 2 institutions in 2 countries.

Adam J BittelResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.ORCID 0000-0003-2134-418X
Sen Chandra SreetamaResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.
Daniel C BittelResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.ORCID 0000-0001-7951-1900
Adam HornResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.
James S NovakResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.ORCID 0000-0002-9989-8724
Toshifumi YokotaDepartment of Medical Genetics, University of Alberta, 116 St. & 85 Ave., Edmonton, AB T6G 2R3, Canada.ORCID 0000-0001-6672-6742
Aiping ZhangResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.
Rika MaruyamaDepartment of Medical Genetics, University of Alberta, 116 St. & 85 Ave., Edmonton, AB T6G 2R3, Canada.ORCID 0000-0002-5656-6930
Kenji Rowel Q LimDepartment of Medical Genetics, University of Alberta, 116 St. & 85 Ave., Edmonton, AB T6G 2R3, Canada.ORCID 0000-0002-5484-4183
Jyoti K JaiswalResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.
Yi-Wen ChenResearch Center for Genetic Medicine, Children's National Hospital, 111 Michigan Ave NW, Washington, DC 20010, USA.
Children's National · USUniversity of Alberta · CA

Funding

Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2016 to 2020
$5.9M
Understanding the mechanism and role of cell membrane repair in Miyoshi MyopathyR01AR055686 · NIAMS · ROCKEFELLER UNIVERSITY · PI JAISWAL, JYOTI K · 2008 to 2021
$3.6M
Genetics and Genomics of Muscle Postdoctoral Training ProgramT32AR056993 · NIAMS · CHILDREN'S RESEARCH INSTITUTE · PI JAISWAL, JYOTI K, PARTRIDGE, TERENCE A · 2010 to 2019
$2.2M
Investigating membrane repair capacity in facioscapulohumeral muscular dystrophyR21HD103993 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI CHEN, YI-WEN · 2021 to 2022
$491k
Friends of FSH Research Research GrantFSHD Global Research Foundation Research GrantFSHD Society Research GrantNIAMS NIH HHS R01 AR055686NIAMS NIH HHS T32 AR056993NICHD NIH HHS R21 HD103993NIH HHS 2T32AR056993NIH HHS R01AR055686NIH HHS U54HD090257Strength, Science, and Stories of Inspiration-Muscular Dystrophy Association Postdoctoral Fellowship Postdoctoral Fellowship
6 · The paper itself

Abstract

Deficits in plasma membrane repair have been identified in dysferlinopathy and Duchenne Muscular Dystrophy, and contribute to progressive myopathy. Although Facioscapulohumeral Muscular Dystrophy (FSHD) shares clinicopathological features with these muscular dystrophies, it is unknown if FSHD is characterized by plasma membrane repair deficits. Therefore, we exposed immortalized human FSHD myoblasts, immortalized myoblasts from unaffected siblings, and myofibers from a murine model of FSHD (

Indexed as

AdultAgedAnimalsAntioxidantsCell MembraneCells, CulturedFemaleGene Expression RegulationHomeodomain ProteinsHumansMaleMiceMiddle AgedMuscle Fibers, SkeletalMuscular Dystrophy, FacioscapulohumeralMyoblastsAntioxidantsDUX4L1 protein, humanHomeodomain ProteinsOligonucleotides, Antisenseantioxidantantisense oligonucleotideDUX4FSHDgapmermembraneMOEmusclemyoblastmyofiberrepair

Identifiers

PMID32759720
PMCPMC7432481
OpenAlexW3047007910

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.