Evidence map›Paper›PMID 18511240›Full record

ReviewJournal of dermatological science2008

Genetically engineered mouse models for skin research: taking the next step.

Jiang Chen, Dennis R Roop

Abstract readReview
In one paragraph

Review in Journal of dermatological science, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Bench approaches to study the detrimental cutaneous impact of tropospheric ozone.Journal of exposure science & environmental epidemiology · 2021
    Review
  4. Animal Models for Studies of Keloid Scarring.Advances in wound care · 2019
    Review
  5. Review
  6. Article
  7. Transgenic mouse technology in skin biology: generation of knockin mice.The Journal of investigative dermatology · 2014
    Article
  8. Article
  9. Animal models of skin disease for drug discovery.Expert opinion on drug discovery · 2013
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. 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

2 authors.

Jiang ChenDepartment of Dermatology and Regenerative Medicine and Stem Cell Biology Program, University of Colorado Denver Health Sciences Center, Aurora, CO 80045, USA.
Dennis R Roop

Funding

Sonic hedgehog in skin /appendage developmentP01AR047898 · NIAMS · BAYLOR COLLEGE OF MEDICINE · PI ROOP, DENNIS · 2001 to 2005
$6.8M
TARGETING ONCOGENE EXPRESSION TO SKIN IN TRANSGENIC MICER01CA052607 · NCI · UNIVERSITY OF COLORADO DENVER · PI ROOP, DENNIS · 1990 to 2015
$6.5M
INDUCIBLE MOUSE MODELS FOR SKIN AND HEAD AND NECK CANCERU01CA105491 · NCI · UNIVERSITY OF COLORADO DENVER · PI ROOP, DENNIS · 2004 to 2009
$4.5M
TESTING GENE THERAPY FOR EPIDERMOLYSIS BULLOSA SIMPLEXR01AR050252 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI ROOP, DENNIS · 2003 to 2007
$1.8M
Regulation and Function of Keratins in the EpidermisR01AR052263 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI ROOP, DENNIS · 2004 to 2010
$1.7M
REGULATION AND FUNCTION OF KERATINS IN THE EPIDERMISR01HD025479 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI ROOP, DENNIS · 1989 to 2003
$1.2M
NCI NIH HHS R01 CA052607NCI NIH HHS U01 CA105491NIAMS NIH HHS P01 AR047898NIAMS NIH HHS R01 AR050252NIAMS NIH HHS R01 AR052263NICHD NIH HHS R01 HD025479
6 · The paper itself

Abstract

Genetically engineered mouse models are invaluable to investigators in nearly all areas of biomedical research. The use of genetically engineered mice has allowed researchers to explore fundamental functions of genes in a mammal that shares substantial similarities with human physiology and pathology. Genetically engineered mice are often used as animal models of human diseases that are vital tools in investigating disease development and in developing and testing novel therapies. Gene targeting in embryonic stem cells allows endogenous genes to be specifically altered. As knowledge regarding precise genetic abnormalities underlying a variety of dermatological conditions continues to emerge, the ability to introduce corresponding alterations in endogenous gene loci in mice, often at a single base pair level, has become essential for detailed studies of these genetic diseases. In this review, we provide examples of mouse models harboring modified endogenous gene(s), generated using the technique commonly referred to as the "knock-in" approach, to exemplify the important and sometimes superior role of this methodology in dermatological research.

Indexed as

Hyperkeratosis, EpidermolyticMice, TransgenicSkin NeoplasmsSkin Physiological PhenomenaAnimalsDisease Models, AnimalGenesGene TargetingKeratinsMiceMice, KnockoutRecombination, GeneticKeratins

Identifiers

PMID18511240
PMCPMC3701407

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.