Evidence map›Paper›PMID 33689290›Full record

ArticleACS chemical neuroscience2021

Synthesis and Assessment of Novel Probes for Imaging Tau Pathology in Transgenic Mouse and Rat Models.

Lindsay McMurray, Jennifer A Macdonald, Nisha Kuzhuppilly Ramakrishnan, Yanyan Zhao, David W Williamson, Ole Tietz, Xiaoyun Zhou, Steven Kealey, Steven G Fagan, Tomáš Smolek and 6 more

Open access · hybridAbstract read
In one paragraph

Article in ACS chemical neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

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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

16 authors at 3 institutions in 2 countries.

Lindsay McMurrayMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Jennifer A MacdonaldMRC Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
Nisha Kuzhuppilly RamakrishnanMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Yanyan ZhaoMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
David W WilliamsonMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Ole TietzMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Xiaoyun ZhouMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Steven KealeyMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Steven G FaganDepartment of Clinical Neurosciences, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Tomáš SmolekAxon Neuroscience R&D Services SE, Bratislava, Slovak Republic 811 02.
Veronika CubinkovaAxon Neuroscience R&D Services SE, Bratislava, Slovak Republic 811 02.
Norbert ŽilkaAxon Neuroscience R&D Services SE, Bratislava, Slovak Republic 811 02.
Maria Grazia SpillantiniDepartment of Clinical Neurosciences, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Aviva M TolkovskyDepartment of Clinical Neurosciences, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Michel GoedertMRC Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
Franklin I AigbirhioMolecular Imaging Chemistry Laboratory, Wolfson Brain Imaging Centre, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.ORCID 0000-0001-9453-5257
University of Cambridge · GBAXON Neuroscience (Slovakia) · SKMRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_U105184291Medical Research Council MR/K02308X/1
6 · The paper itself

Abstract

Aggregated tau protein is a core pathology present in several neurodegenerative diseases. Therefore, the development and application of positron emission tomography (PET) imaging radiotracers that selectively bind to aggregated tau in fibril form is of importance in furthering the understanding of these disorders. While radiotracers used in human PET studies offer invaluable insight, radiotracers that are also capable of visualizing tau fibrils in animal models are important tools for translational research into these diseases. Herein, we report the synthesis and characterization of a novel library of compounds based on the phenyl/pyridinylbutadienylbenzothiazoles/benzothiazolium (PBB3) backbone developed for this application. From this library, we selected the compound LM229, which binds to recombinant tau fibrils with high affinity (

Indexed as

Alzheimer Diseasetau ProteinsAnimalsBrainMiceMice, TransgenicNeurofibrillary TanglesPositron-Emission TomographyRatsRats, Transgenictau ProteinsimagingmouseneurodegenerationPETrattau

Identifiers

PMID33689290
PMCPMC8176454
OpenAlexW3133688088

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.