Evidence map›Paper›PMID 36009526›Full record

ReviewBiomedicines2022

Protein Kinase CK2 and Its Potential Role as a Therapeutic Target in Huntington's Disease.

Angel White, Anna McGlone, Rocio Gomez-Pastor

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Silmitasertib, an FDA-designated orphan CK2 inhibitor, ameliorates neuropathology and motor dysfunction in a Huntington's disease mouse model.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  3. Article
  4. 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

3 authors at 1 institution in 1 country.

Angel WhiteDepartment of Neuroscience, School of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Anna McGloneDepartment of Neuroscience, School of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Rocio Gomez-PastorDepartment of Neuroscience, School of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0003-1136-5462
University of Minnesota · US

Funding

Molecular mechanisms of synaptic dysfunction and cognitive decline in Huntington's diseaseR01NS110694 · NINDS · UNIVERSITY OF MINNESOTA · PI Rocio Gomez-Pastor · 2020 to 2026
$3.1M
Chemical Probes as Allosteric Modulators of CK2 Alpha Prime Targeting Huntington's DiseaseR21NS116260 · NINDS · UNIVERSITY OF MINNESOTA · PI GOMEZ-PASTOR, ROCIO · 2021 to 2022
$417k
NINDS NIH HHS R01 NS110694NINDS NIH HHS R01NS110694NINDS NIH HHS R21 NS116260NINDS NIH HHS R21NS116260
6 · The paper itself

Abstract

Huntington's Disease (HD) is a devastating neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the

Indexed as

CK2HTT phosphorylationHuntington’s diseasekinase inhibitionpost-translation modifications

Identifiers

PMID36009526
PMCPMC9406209
OpenAlexW4291742956

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.