Evidence map›Paper›PMID 22189787›Full record

ReviewThe Journal of investigative dermatology2012

Desmoglein as a target in skin disease and beyond.

Masayuki Amagai, John R Stanley

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of investigative dermatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
11.7field-weighted citation impact, top 1% 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

95 citing papers in PubMed, 200 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Review
  5. Article
  6. UltrastrongScience advances · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Desmosomes at a glance.Journal of cell science · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

35 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 2 countries.

Masayuki AmagaiDepartment of Dermatology, Keio University School of Medicine, Tokyo, Japan.
John R Stanley
Keio University · JPUniversity of Pennsylvania · US

Funding

Cloning and genetics of human pemphigus autoantibodiesR01AR052672 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI STANLEY, JOHN R · 2006 to 2015
$3.7M
Understanding molecular mechanisms underlying the formation of the blue nevus andP30AR057217 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI STANLEY, JOHN R · 2009 to 2013
$3.2M
Mechanisms of Blister Formation by Staphylococcal ToxinsR01AR048223 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI STANLEY, JOHN R · 2002 to 2006
$1.9M
PATHOGENESIS OF PEMPHIGUSR01AR045437 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI STANLEY, JOHN R · 1998 to 2001
$658k
FUNCTION OF PEMPHIGUS VULGARIS ANTIGENR01AR043776 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI STANLEY, JOHN R · 1996 to 2000
$252k
NIAMS NIH HHS P30 AR057217NIAMS NIH HHS R01 AR043776NIAMS NIH HHS R01 AR045437NIAMS NIH HHS R01 AR048223NIAMS NIH HHS R01 AR052672
6 · The paper itself

Abstract

Much of the original research on desmosomes and their biochemical components was through analysis of skin and mucous membranes. The identification of desmogleins 1 and 3, desmosomal adhesion glycoproteins, as targets in pemphigus, a fatal autoimmune blistering disease of the skin and mucous membranes, provided the first link between desmosomes, desmogleins, and human diseases. The clinical and histological similarities of staphylococcal scalded skin syndrome or bullous impetigo and pemphigus foliaceus led us to identify desmoglein 1 as the proteolytic target of staphylococcal exfoliative toxins. Genetic analysis of striate palmoplantar keratoderma and hypotrichosis identified their responsible genes as desmogleins 1 and 4, respectively. More recently, these fundamental findings in cutaneous biology were extended beyond the skin. Desmoglein 2, which is expressed earliest among the four isoforms of desmoglein in development and found in all desmosome-bearing epithelial cells, was found to be mutated in arrythmogenic right ventricular cardiomyopathy and has also been identified as a receptor for a subset of adenoviruses that cause respiratory and urinary tract infections. The story of desmoglein research illuminates how dermatological research, originally focused on one skin disease, pemphigus, has contributed to understanding the biology and pathophysiology of many seemingly unrelated tissues and diseases.

Indexed as

CardiomyopathiesDesmoglein 1Desmoglein 2Desmoglein 3DesmogleinsHumansHypertrichosisKeratoderma, PalmoplantarPemphigusDesmoglein 1Desmoglein 2Desmoglein 3DesmogleinsDSG1 protein, humanDSG2 protein, humanDSG3 protein, humanDSG4 protein, human

Identifiers

PMID22189787
PMCPMC3279627
OpenAlexW1991526125

What OpenQuestion holds

Textmetadata
LicenceTDM
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.