Evidence map›Paper›PMID 24665072›Full record

ReviewAmerican journal of medical genetics. Part A2014

Modeling AEC-New approaches to study rare genetic disorders.

Peter J Koch, Jason Dinella, Mary Fete, Elaine C Siegfried, Maranke I Koster

Open access · greenAbstract readReview
In one paragraph

Review in American journal of medical genetics. Part A, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Use of induced pluripotent stem cells in dermatological research.The Journal of investigative dermatology · 2014
    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 3 institutions in 1 country.

Peter J KochDepartment of Dermatology, University of Colorado School of Medicine, Aurora, Colorado; Department of Cell and Developmental Biology, University of Colorado School of Medicine, Aurora, Colorado; Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado School of Medicine, Aurora, Colorado; Graduate Program in Cell Biology, Stem Cells and Development, University of Colorado School of Medicine, Aurora, Colorado.
Jason Dinella
Mary Fete
Elaine C Siegfried
Maranke I Koster
Gates (United States) · USNational Foundation for Ectodermal Dysplasias · USSaint Louis University · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Transgenic and Gene Targeting CoreP30AR057212 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI NORRIS, DAVID A. · 2009 to 2018
$6.2M
Cross-talk Between Desmosomal Proteins and Signaling Pathways in the SkinR01AR053892 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI KOCH, PETER J. · 2008 to 2012
$1.9M
The role of p63 in hair follicle stem cells and cancerR01AR061506 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI KOSTER, MARANKE I. · 2011 to 2015
$1.7M
Elucidating the molecular pathology of ectodermal dysplasias caused by TP63 mutatR56AR066713 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI KOCH, PETER J., KOSTER, MARANKE I. · 2014 to 2015
$918k
The role of p63 in normal epidermal differentiation and ectodermal dysplasiasR00AR054696 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI KOSTER, MARANKE I. · 2009 to 2011
$747k
NCATS NIH HHS UL1 TR001082NIAMS NIH HHS P30 AR057212NIAMS NIH HHS R00 AR054696NIAMS NIH HHS R01 AR053892NIAMS NIH HHS R01 AR061506NIAMS NIH HHS R56 AR066713
6 · The paper itself

Abstract

Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome is a rare monogenetic disorder that is characterized by severe abnormalities in ectoderm-derived tissues, such as skin and its appendages. A major cause of morbidity among affected infants is severe and chronic skin erosions. Currently, supportive care is the only available treatment option for AEC patients. Mutations in TP63, a gene that encodes key regulators of epidermal development, are the genetic cause of AEC. However, it is currently not clear how mutations in TP63 lead to the various defects seen in the patients' skin. In this review, we will discuss current knowledge of the AEC disease mechanism obtained by studying patient tissue and genetically engineered mouse models designed to mimic aspects of the disorder. We will then focus on new approaches to model AEC, including the use of patient cells and stem cell technology to replicate the disease in a human tissue culture model. The latter approach will advance our understanding of the disease and will allow for the development of new in vitro systems to identify drugs for the treatment of skin erosions in AEC patients. Further, the use of stem cell technology, in particular induced pluripotent stem cells (iPSC), will enable researchers to develop new therapeutic approaches to treat the disease using the patient's own cells (autologous keratinocyte transplantation) after correction of the disease-causing mutations.

Indexed as

AnimalsCleft LipCleft PalateDisease Models, AnimalEctodermal DysplasiaEpidermisEye AbnormalitiesEyelidsHumansInduced Pluripotent Stem CellsMutationTumor Suppressor ProteinsTumor Suppressor Proteinsankyloblepharon-ectodermal defects-cleft lip/palate syndrome (AEC)ectodermal dysplasiagenodermatosesinduced pluripotent stem cellsinherited skin disordersin vitro disease modelsiPSC-based cell therapyiPSC-derived keratinocytesiPS cellsskin equivalentsTP63

Identifiers

PMID24665072
PMCPMC4526214
OpenAlexW2011389696

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.