Evidence map›Paper›PMID 26551941›Full record

ReviewThe journal of investigative dermatology. Symposium proceedings2015

Excavating the Genome: Large-Scale Mutagenesis Screening for the Discovery of New Mouse Models.

John P Sundberg, Soheil S Dadras, Kathleen A Silva, Victoria E Kennedy, Stephen A Murray, James M Denegre, Paul N Schofield, Lloyd E King, Michael V Wiles, C Herbert Pratt

Open access · bronzeAbstract readReview
In one paragraph

Review in The journal of investigative dermatology. Symposium proceedings, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

10 authors at 4 institutions in 2 countries.

John P SundbergDepartments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
Soheil S DadrasDepartment of Dermatology, University of Connecticut, Farmington, Connecticut, USA.
Kathleen A SilvaDepartments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
Victoria E KennedyDepartments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
Stephen A MurrayDepartment of Genetic Resources Science, The Jackson Laboratory, Bar Harbor, Maine, USA.
James M DenegreDepartment of Genetic Resources Science, The Jackson Laboratory, Bar Harbor, Maine, USA.
Paul N SchofieldDepartments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
Lloyd E KingDivision of Dermatology, Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
Michael V WilesDepartment of Technology Evaluation and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
C Herbert PrattDepartment of Genetic Resources Science, The Jackson Laboratory, Bar Harbor, Maine, USA.
Jackson Laboratory · USVanderbilt University · USUniversity of Cambridge · GBUniversity of Connecticut · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
High Throughput Production and Cryopreservation of Knockout MiceU42OD011185 · OD · JACKSON LABORATORY · PI MURRAY, STEPHEN A, TAFT, ROBERT A · 2012 to 2015
$17.9M
Mouse Models of Human Cancer DatabaseR01CA089713 · NCI · JACKSON LABORATORY · PI BULT, CAROL J · 2002 to 2025
$17.5M
CRE Driver Strain ResourcesR24OD011190 · OD · JACKSON LABORATORY · PI MURRAY, STEPHEN A, SMITH, CYNTHIA LOUISE · 2012 to 2022
$7.9M
Cpdm: Cloning a Gene That Regulates Eosinophil FunctionR01AR049288 · NIAMS · JACKSON LABORATORY · PI BOWCOCK, ANNE MARY, HOGENESCH, HARM · 2004 to 2016
$5.9M
Skeletal Phenotyping of KOMP MiceR01AR063702 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ACKERT-BICKNELL, CHERYL LYNNE, ROWE, DAVID W. · 2013 to 2017
$3.2M
Model Systems for PXER01AR055225 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI UITTO, JOUNI · 2008 to 2017
$3.2M
Genetics of Alopecia Areata in the C3H/HeJ MouseR01AR056635 · NIAMS · JACKSON LABORATORY · PI SUNDBERG, JOHN PAUL · 2010 to 2014
$1.9M
Discovering Novel Gene Networks for Skin DiseasesR21AR063781 · NIAMS · JACKSON LABORATORY · PI SUNDBERG, JOHN PAUL · 2013 to 2014
$422k
Accelerating Autoimmune Treatments through Alopecia Areata ResearchR13AR067088 · NIAMS · NATIONAL ALOPECIA AREATA FOUNDATION · PI NORRIS, DAVID A. · 2014 to 2015
$40k
NCI NIH HHS P30 CA034196NCI NIH HHS P30-CA34196NCI NIH HHS R01 CA089713NCI NIH HHS R01-CA089713NIAMS NIH HHS R01 AR049288NIAMS NIH HHS R01 AR055225NIAMS NIH HHS R01 AR056635NIAMS NIH HHS R01 AR063702NIAMS NIH HHS R13 AR067088NIAMS NIH HHS R13-AR067088-01NIAMS NIH HHS R21 AR063781NIAMS NIH HHS R21-AR063781NIH HHS OD011190NIH HHS U42 OD011185
6 · The paper itself

Abstract

Technology now exists for rapid screening of mutated laboratory mice to identify phenotypes associated with specific genetic mutations. Large repositories exist for spontaneous mutants and those induced by chemical mutagenesis, many of which have never been fully studied or comprehensively evaluated. To supplement these resources, a variety of techniques have been consolidated in an international effort to create mutations in all known protein coding genes in the mouse. With targeted embryonic stem cell lines now available for almost all protein coding genes and more recently CRISPR/Cas9 technology, large-scale efforts are underway to create further novel mutant mouse strains and to characterize their phenotypes. However, accurate diagnosis of skin, hair, and nail diseases still relies on careful gross and histological analysis, and while not automated to the level of the physiological phenotyping, histopathology still provides the most direct and accurate diagnosis and correlation with human diseases. As a result of these efforts, many new mouse dermatological disease models are being characterized and developed.

Indexed as

Disease Models, AnimalDNA Mutational AnalysisAlopecia AreataAnimalsGenomeHumansMiceMice, KnockoutPhenotype

Identifiers

PMID26551941
PMCPMC4734626
OpenAlexW2179640974

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.