Evidence map›Paper›PMID 7489712›Full record

ArticleThe EMBO journal1995

A synthetic, chemically modified ribozyme eliminates amelogenin, the major translation product in developing mouse enamel in vivo.

S P Lyngstadaas, S Risnes, B S Sproat, P S Thrane, H P Prydz

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.5field-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.

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

27 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Protein-mediated enamel mineralization.Frontiers in bioscience (Landmark edition) · 2012
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Enamel matrix proteins; old molecules for new applications.Orthodontics & craniofacial research · 2009
    Review
  12. A mouse model expressing a truncated form of ameloblastin exhibits dental and junctional epithelium defects.Matrix biology : journal of the International Society for Matrix Biology · 2009
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 3. Protein-protein interactions of the developing enamel matrix.Current topics in developmental biology · 2006
    Review
  18. Article
  19. Functional domains for amelogenin revealed by compound genetic defects.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2003
    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

5 authors at 1 institution in 2 countries.

S P LyngstadaasBiotechnology Centre of Oslo, The National Hospital, University of Oslo, Norway.
S Risnes
B S Sproat
P S Thrane
H P Prydz
Oslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribozymes are small RNA structures capable of cleaving RNA target molecules in a catalytic fashion. Designed ribozymes can be targeted to specific mRNAs, blocking their expression without affecting normal functions of other genes. Because of their specific and catalytic mode of action ribozymes are ideal agents for therapeutic interventions against malfunctioning or foreign gene products. Here we report successful experiments to 'knock out' a major translation product in vivo using synthesized, chemically modified ribozymes. The ribozymes, designed to cleave amelogenin mRNA, were injected close to developing mandibular molar teeth in newborn mice, resulting in a prolonged and specific arrest of amelogenin synthesis not caused by general toxicity. No carriers were required to assist cellular uptake. Amelogenins are highly conserved tissue-specific proteins that play a central role in mammalian enamel biomineralization. Ultrastructural analyses of in vivo ribozyme-treated teeth demonstrated their failure to develop normally mineralized enamel. These results demonstrate that synthesized ribozymes can be highly effective in achieving both timed and localized 'knock-out' of important gene products in vivo, and suggest new possibilities for suppression of gene expression for research and therapeutic purposes.

Indexed as

AmelogeninAnimalsAnimals, NewbornBase SequenceDental EnamelDental Enamel ProteinsMiceMice, Inbred BALB CMicroscopy, Electron, ScanningMolecular Sequence DataRNA, CatalyticAmelogeninAmelx protein, mouseDental Enamel ProteinsRNA, Catalytic

Identifiers

PMID7489712
PMCPMC394632
OpenAlexW2133245471

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.