Evidence map›Paper›PMID 22811267›Full record

ArticleThe International journal of developmental biology2012

Identification and characterization of ADAM41, a novel ADAM metalloproteinase in Xenopus.

Guofeng Xu, Shuo Wei, Judith M White, Douglas W DeSimone

Abstract read
In one paragraph

Article in The International journal of developmental biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 90% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 1 country.

Guofeng XuDepartment of Cell Biology and the Morphogenesis and Regenerative Medicine Institute, University of Virginia, Charlottesville, VA 22908, USA.
Shuo Wei
Judith M White
Douglas W DeSimone
University of Virginia · US

Funding

Cell-Cell and Cell-Matrix Interactions in MorphogenesisR01GM094793 · NIGMS · UNIVERSITY OF VIRGINIA · PI DESIMONE, DOUGLAS W. · 2010 to 2017
$3.3M
ADAM FUNCTION IN NEURAL CREST CELLSR01DE014365 · NIDCR · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI DESIMONE, DOUGLAS W. · 2002 to 2006
$1.8M
NIDCR NIH HHS DE14365NIDCR NIH HHS R01 DE014365NIGMS NIH HHS GM094793NIGMS NIH HHS R01 GM094793
6 · The paper itself

Abstract

The ADAM family of transmembrane metalloproteinases has important functions in fertilization, development and disease, and is widely distributed throughout the Metazoa. In this study, we identified a novel ADAM protein in Xenopus tropicalis (X. tropicalis) with closest overall sequence similarity to the Xenopus ADAM10 protein. Based on comparisons of available sequence information, putative orthologs of this ADAM (which we designate ADAM41) are identified in several other vertebrate species including non-placental mammals, but absent from placental mammals and aves. ADAM41 mRNA is maternally deposited in X. tropicalis with subsequent zygotic expression detected in the neural plate at neurula stages. Antisense morpholino knockdown of ADAM41 results in a delay in early neuronal marker expression, which can be rescued by a non-targeted ADAM41 transcript. Thus, ADAM41 is likely required for maintaining proper timing of neurogenesis in X. tropicalis.

Indexed as

Gene Expression Regulation, DevelopmentalADAM ProteinsAmino Acid SequenceAnimalsBlotting, WesternEmbryo, NonmammalianIn Situ HybridizationMolecular Sequence DataNeuronsOligonucleotides, AntisensePhylogenySequence Homology, Amino AcidXenopus laevisXenopus ProteinsADAM ProteinsOligonucleotides, AntisenseXenopus Proteins

Identifiers

PMID22811267
PMCPMC3695402
OpenAlexW2070677428

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.