Evidence map›Paper›PMID 8983017›Full record

ReviewMolecular biology reports1996

Molecular complexity of the cutaneous basement membrane zone.

J Uitto, L Pulkkinen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Revertant mosaicism in genodermatoses.Cellular and molecular life sciences : CMLS · 2017
    Review
  7. Article
  8. Gene therapy for skin diseases.Cold Spring Harbor perspectives in medicine · 2014
    Review
  9. The corneal epithelial basement membrane: structure, function, and disease.Investigative ophthalmology & visual science · 2013
    Review
  10. Article
  11. Article
  12. Collagens.Cell and tissue research · 2010
    Review
  13. Review
  14. Article
  15. Dilated cardiomyopathy in dystrophic epidermolysis bullosa.Archives of disease in childhood · 2000
    Review
  16. Article
  17. Article
  18. Cellular and molecular partners involved in gut morphogenesis and differentiation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 1998
    Review
  19. Article
  20. Article
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 1 country.

J UittoDepartment of Dermatology, Jefferson Medical College, Philadelphia, PA 19107, USA.
L Pulkkinen
Jefferson College · USThomas Jefferson University · US

Funding

TRANSGENIC MICE WITH EPIDERMOLYSIS BULLOSAP01AR038923 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI UITTO, JOUNI · 1987 to 2006
$7.8M
NIAMS NIH HHS P01 AR38923
6 · The paper itself

Abstract

Ultrastructural examination of the cutaneous basement membrane zone (BMZ) reveals the presence of several attachment structures, which are critical for integrity of the stable association of epidermis and dermis. These include hemidesmosomes which extend from the intracellular compartment of the basal keratinocyte to the underlying basement membrane where they complex with anchoring filaments, thread-like structures traversing the lamina lucida. At the lower portion of dermal-epidermal attachment zone, anchoring fibrils extend from the lamina densa to the papillary dermis, where they associate with basement membrane-like structures, known as anchoring plaques. Molecular cloning of the cutaneous BMZ components has allowed elucidation of the structural features of the proteins which constitute these attachment structures. Specifically, hemidesmosomes have been shown to consist of at least four distinct proteins. The intracellular hemidesmosomal inner plaque is comprised of the 230-kD bullous pemphigoid antigen (BPAG1), and plectin, a high-molecular weight cytomatrix protein, encoded by the corresponding gene, PLEC1. The transmembrane component of the hemidesmosomes consists of the 180-kD bullous pemphigoid antigen (BPAG2), a collagenous protein also known as type XVII collagen (COL17A1), as well as of the basal keratinocyte-specific integrin alpha 6 beta 4. The anchoring filaments consist predominantly of laminin 5 with three constitutive subunit polypeptides, the alpha 3, beta 3 and gamma 2 chains, which is associated with laminin 6 with the chain composition alpha 3, beta 1 and gamma 1. Also associated with anchoring filaments is a novel protein, ladinin, which serves as autoantigen in the linear IgA disease, and the corresponding gene, LAD1, has been mapped to human chromosome 1. Finally, the major, if not the exclusive, component of anchoring fibrils is type VII collagen, encoded by the gene (COL7A1) which consists of 118 distinct exons, the largest number of exons in any gene published thus far. Collectively, the cutaneous basement membrane zone is a complex continuum of macromolecules which form a network providing the stable association of the epidermis to the underlying dermis. Thus, genetic lesions resulting in abnormalities in any part of this network could result in a blistering skin disease, such as epidermolysis bullosa.

Indexed as

Carrier ProteinsCytoskeletal ProteinsNerve Tissue ProteinsNon-Fibrillar CollagensAntigens, CDAutoantigensBasement MembraneCollagenCollagen Type XVIIDesmosomesDystoninEpidermisExtracellular Matrix ProteinsGenetic Diseases, InbornHumansIntegrin alpha6Antigens, CDAutoantigensCarrier ProteinsCollagenCollagen Type XVIICytoskeletal ProteinsDST protein, humanDystoninExtracellular Matrix ProteinsIntegrin alpha6Integrin beta4Intermediate Filament ProteinsLad1 protein, mouseLamininMembrane GlycoproteinsNerve Tissue ProteinsNon-Fibrillar CollagensPLEC protein, humanPlectin

Identifiers

PMID8983017
OpenAlexW2082999868

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.