Evidence map›Paper›PMID 36167646›Full record

ReviewCold Spring Harbor perspectives in biology2023

Stairways to Advanced Therapies for Epidermolysis Bullosa.

Laura De Rosa, Elena Enzo, Michele Palamenghi, Laura Sercia, Michele De Luca

Open access · greenAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. A cellular disease model toward gene therapy ofMolecular therapy. Methods & clinical development · 2024
    Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Allele-specific CRISPR-Cas9 editing of dominant epidermolysis bullosa simplex in human epidermal stem cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  11. Decoding the Human Epidermal Complexity at Single-Cell Resolution.International journal of molecular sciences · 2023
    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

5 authors at 3 institutions in 1 country.

Laura De Rosa *Holostem Terapie Avanzate, S.r.l., 41125 Modena, Italy.
Elena Enzo *Centre for Regenerative Medicine "Stefano Ferrari," University of Modena and Reggio Emilia, 41125 Modena, Italy.
Michele Palamenghi *Centre for Regenerative Medicine "Stefano Ferrari," University of Modena and Reggio Emilia, 41125 Modena, Italy.
Laura Sercia *Centre for Regenerative Medicine "Stefano Ferrari," University of Modena and Reggio Emilia, 41125 Modena, Italy.
Michele De LucaCentre for Regenerative Medicine "Stefano Ferrari," University of Modena and Reggio Emilia, 41125 Modena, Italy michele.deluca@unimore.it.
Ferrari (Italy) · ITUniversity of Modena and Reggio Emilia · ITTecnologie Avanzate (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermolysis bullosa (EB) is a devastating genetic skin disease typified by a plethora of different phenotypes and ranking from severe, early lethal, to mild localized forms. Although there is no cure for EB, recent progress in pharmacology and molecular and cellular biology is boosting the development of new advanced therapeutic strategies. Here we will focus on two main categories of such therapies: (1) those aimed at controlling inflammation and inducing reepithelialization of the wounds, and (2) those, perhaps more challenging and ambitious, that aim to permanently regenerate a fully functional epidermis, which requires targeting of epidermal stem cells. In both cases, the genetic variants underlying the different EB forms and factors, such as genetic background, modifier genes, comorbidities, and lifestyle, all of which impinge on EB genotype-phenotype correlation, need to be defined.

Indexed as

Epidermolysis BullosaEpidermisHumansPhenotype

Identifiers

PMID36167646
PMCPMC10071437
OpenAlexW4297339765

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.