Evidence map›Paper›PMID 27638769›Full record

ArticleBiology open2016

Adamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development.

Dalya Ataca, Marian Caikovski, Alessandra Piersigilli, Alexandre Moulin, Charaf Benarafa, Sarah E Earp, Yakir Guri, Corinne Kostic, Yvan Arsenijevic, Raija Soininen and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  8. ADAMTS18Nature communications · 2022
    Article
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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

12 authors at 6 institutions in 3 countries.

Dalya AtacaEcole Polytechnique Fédérale de Lausanne, ISREC, NCCR Molecular Oncology, Station 19, Lausanne CH-1015, Switzerland.
Marian CaikovskiEcole Polytechnique Fédérale de Lausanne, ISREC, NCCR Molecular Oncology, Station 19, Lausanne CH-1015, Switzerland.
Alessandra PiersigilliEcole Polytechnique Fédérale de Lausanne, ISREC, NCCR Molecular Oncology, Station 19, Lausanne CH-1015, Switzerland.
Alexandre MoulinJules-Gonin Eye Hospital, University of Lausanne, Avenue de France 15, Lausanne CH-1004, Switzerland.
Charaf BenarafaTheodor Kocher Institute, University of Bern, Freiestrasse 1, Bern CH-3012, Switzerland.
Sarah E EarpBiomedical Engineering-ND20, Cleveland Clinic Lerner Research Institute, 9500 Euclid Ave., Cleveland, OH 44195, USA.
Yakir GuriEcole Polytechnique Fédérale de Lausanne, ISREC, NCCR Molecular Oncology, Station 19, Lausanne CH-1015, Switzerland.
Corinne KosticJules-Gonin Eye Hospital, University of Lausanne, Avenue de France 15, Lausanne CH-1004, Switzerland.
Yvan ArsenijevicJules-Gonin Eye Hospital, University of Lausanne, Avenue de France 15, Lausanne CH-1004, Switzerland.
Raija SoininenDepartment of Pathology, Biocenter Oulu, University of Oulu, Oulu FIN-90014, Finland.
Suneel S ApteBiomedical Engineering-ND20, Cleveland Clinic Lerner Research Institute, 9500 Euclid Ave., Cleveland, OH 44195, USA.
Cathrin BriskenEcole Polytechnique Fédérale de Lausanne, ISREC, NCCR Molecular Oncology, Station 19, Lausanne CH-1015, Switzerland cathrin.brisken@epfl.ch.ORCID 0000-0002-6857-3230
École Polytechnique Fédérale de Lausanne · CHHôpital Ophtalmique Jules-Gonin · CHCleveland Clinic Lerner College of Medicine · USUniversity of Basel · CHUniversity of Bern · CHUniversity of Oulu · FI

Funding

Extracellular matrix remodeling in ocular anterior segment developmentR01EY024943 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI APTE, SUNEEL S · 2015 to 2017
$1.1M
Cole Eye Institute Vision Science Training ProgramT32EY024236 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI ANAND-APTE, BELA · 2015 to 2025
$1.0M
NEI NIH HHS R01 EY024943NEI NIH HHS T32 EY024236
6 · The paper itself

Abstract

The ADAMTS family comprises 19 secreted metalloproteinases that cleave extracellular matrix components and have diverse functions in numerous disease and physiological contexts. A number of them remain 'orphan' proteases and among them is ADAMTS18, which has been implicated in developmental eye disorders, platelet function and various malignancies. To assess in vivo function of ADAMTS18, we generated a mouse strain with inactivated Adamts18 alleles. In the C57Bl6/Ola background, Adamts18-deficient mice are born in a normal Mendelian ratio, and are viable but show a transient growth delay. Histological examination revealed a 100% penetrant eye defect resulting from leakage of lens material through the lens capsule occurring at embryonic day (E)13.5, when the lens grows rapidly. Adamts18-deficient lungs showed altered bronchiolar branching. Fifty percent of mutant females are infertile because of vaginal obstruction due to either a dorsoventral vaginal septum or imperforate vagina. The incidence of ovarian rete is increased in the mutant mouse strain. Thus, Adamts18 is essential in the development of distinct tissues and the new mouse strain is likely to be useful for investigating ADAMTS18 function in human disease, particularly in the contexts of infertility and carcinogenesis.

Indexed as

Adamts18Lens capsuleLung developmentMetalloproteinaseRete ovaryVaginal septum

Identifiers

PMID27638769
PMCPMC5155532
OpenAlexW2520280612

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.