Evidence map›Paper›PMID 40226336›Full record

ArticleRSC chemical biology2025

A stress-responsive p38 signaling axis in choanoflagellates.

Florentine U Rutaganira, Maxwell C Coyle, Maria H T Nguyen, Iliana Hernandez, Alex P Scopton, Arvin C Dar, Nicole King

Abstract read
In one paragraph

Article in RSC chemical biology, 2025. 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
–field-weighted citation impact
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.

  1. Article
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

7 authors.

Florentine U RutaganiraDepartment of Biochemistry, Stanford University School of Medicine Stanford CA 94305 USA funr@stanford.edu.ORCID https://orcid.org/0000-0001-5587-1872
Maxwell C CoyleHoward Hughes Medical Institute and the Department of Molecular and Cell Biology, University of California Berkeley CA 94720 USA.ORCID https://orcid.org/0009-0009-8874-4699
Maria H T NguyenDepartment of Biology, Stanford University Stanford CA 94305 USA.ORCID https://orcid.org/0000-0003-2441-4948
Iliana HernandezDepartment of Biochemistry, Stanford University School of Medicine Stanford CA 94305 USA funr@stanford.edu.
Alex P ScoptonDepartment of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai New York NY 10029 USA.
Arvin C DarDepartment of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai New York NY 10029 USA.ORCID https://orcid.org/0000-0003-0318-4848
Nicole KingHoward Hughes Medical Institute and the Department of Molecular and Cell Biology, University of California Berkeley CA 94720 USA.ORCID https://orcid.org/0000-0002-6409-1111

Funding

Targeting Oncogenic Ras-MAPK Signaling Complexes via the Scaffold KSRR01CA227636 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Arvin Dar · 2018 to 2026
$4.0M
AN INTEGRATED PLATFORM FOR NOVEL PERSONALIZED LIVER CANCER THERAPEUTICSR01CA256480 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DAR, ARVIN, GUCCIONE, ERNESTO · 2021 to 2025
$3.3M
A Chemical Genetic Approach to Exploring Novel Therapeutic Space for Colorectal CancerR01CA258736 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI DAR, ARVIN · 2021 to 2025
$3.2M
Automated High-Throughput, High-Content Confocal/Wide-Field Microscope SystemS10OD021828 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI WEST, MARY · 2017 to 2017
$1.0M
A Cytochrome P450 Therapeutic Space for TauopathiesR56AG066712 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAGAN, ROSS LEIGH, DAR, ARVIN · 2021 to 2021
$802k
NCI NIH HHS R01 CA227636NCI NIH HHS R01 CA256480NCI NIH HHS R01 CA258736NIA NIH HHS R56 AG066712NIH HHS S10 OD021828
6 · The paper itself

Abstract

Animal kinases regulate cellular responses to environmental stimuli, including cell differentiation, migration, survival, and response to stress, but the ancestry of these functions is poorly understood. Choanoflagellates, the closest living relatives of animals, encode homologs of diverse animal kinases and have emerged as model organisms for reconstructing animal origins. However, efforts to identify key kinase regulators in choanoflagellates have been constrained by the limitations of currently available genetic tools. Here, we report on a framework that combines small molecule-driven kinase discovery with targeted genetics to reveal kinase function in choanoflagellates. To study the physiological roles of choanoflagellate kinases, we established two high-throughput platforms to screen the model choanoflagellate

Identifiers

PMID40226336
PMCPMC11984502

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.