Evidence map›Paper›PMID 26802230›Full record

ReviewThe Journal of investigative dermatology2016

Progress toward Treatment and Cure of Epidermolysis Bullosa: Summary of the DEBRA International Research Symposium EB2015.

Jouni Uitto, Leena Bruckner-Tuderman, Angela M Christiano, John A McGrath, Cristina Has, Andrew P South, Brett Kopelan, E Clare Robinson

Registry-linked trialOpen access · greenAbstract readComparative StudyReview
In one paragraph

Review in The Journal of investigative dermatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03269474 (Computational Drug Repurposing for All Epidermolysis Bullosa Simplex), which is not on this map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
7.2field-weighted citation impact, top 3% 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.

NCT03269474 unknown statusnot on this mapstarted 2017, after this paper: background citation

Computational Drug Repurposing for All Epidermolysis Bullosa Simplex (EBS) Cases

TypeobservationalSponsorJoyce TengRan2017 to 2024Enrolled60ConditionsEpidermolysis Bullosa, Healthy, Genetic Skin Disease, Epidermolysis Bullosa SimplexArmsExperimental Group
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 73 citations in OpenAlex.

  1. Trial
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  5. Review
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  7. Challenges of Gene Editing Therapies for Genodermatoses.International journal of molecular sciences · 2023
    Review
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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 7 institutions in 4 countries.

Jouni UittoDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. Electronic address: Jouni.Uitto@jefferson.edu.
Leena Bruckner-TudermanDepartment of Dermatology, Medical Center, University of Freiburg, Freiburg, Germany.
Angela M ChristianoDepartment of Dermatology, Columbia University, New York, New York, USA.
John A McGrathGenetic Skin Disease Group, St. John's Institute of Dermatology, King's College London (Guy's Campus), London, UK.
Cristina HasDepartment of Dermatology, Medical Center, University of Freiburg, Freiburg, Germany.
Andrew P SouthDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Brett KopelanDEBRA of America, New York, New York, USA.
E Clare RobinsonDEBRA International, Vienna, Austria.
Thomas Jefferson University · USColumbia University · USDebra · ATDystrophic Epidermolysis Bullosa Research Association of America · USKing's College London · GBUniversity Medical Center Freiburg · DEUniversity of Freiburg · DE

Funding

EB2015: DEBRA International Symposium on Epidermolysis BullosaR13AR068235 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI UITTO, JOUNI · 2015 to 2015
$30k
NIAMS NIH HHS R13 AR068235NIAMS NIH HHS R13AR068235
6 · The paper itself

Abstract

Epidermolysis bullosa (EB), a group of complex heritable blistering diseases, is the topic of triennial research meetings organized by DEBRA International, Vienna, Austria, the network of national EB patient advocacy organizations. The DEBRA 2015 Research Conference, held in May 2015, brought together investigators and clinicians from around the world working at the forefront of EB research. Discussing the state-of-the-art approaches from a wide range of disciplines, there was a palpable excitement at this conference brought about by the optimism about applying new sequencing techniques, genome editing, protein replacement, autologous and allogeneic stem cell therapy, innovations in cancer biology, revertant mosaicism, and induced pluripotent stem cell techniques, all of which are aimed at developing new therapies for EB. Many in the field who have participated in EB research for many years were especially enthusiastic and felt that, possibly for the first time, the field seems uniquely poised to bring these new tools to effectively tackle EB. Multiple complementary approaches are currently in motion toward improved quality of life and eventually a cure for patients suffering from EB, a currently intractable disease.

Indexed as

AnimalsAustriaBone Marrow TransplantationCongresses as TopicDisease Models, AnimalDrosophilaEpidermolysis BullosaForecastingGenetic TherapyHumansInternationalityMiceMolecular Targeted TherapyStem Cell TransplantationTreatment OutcomeZebrafish

Identifiers

PMID26802230
PMCPMC4724642
OpenAlexW2287953832

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.