Evidence map›Paper›PMID 33749590›Full record

ArticleeLife2021

Genetic disruption of WASHC4 drives endo-lysosomal dysfunction and cognitive-movement impairments in mice and humans.

Jamie L Courtland, Tyler Wa Bradshaw, Greg Waitt, Erik J Soderblom, Tricia Ho, Anna Rajab, Ricardo Vancini, Il Hwan Kim, Scott H Soderling

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 51 citations in OpenAlex.

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  20. Case report: A novelFrontiers in genetics · 2023
    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

9 authors at 2 institutions in 1 country.

Jamie L Courtland *Department of Neurobiology, Duke University School of Medicine, Durham, United States.ORCID 0000-0001-6846-3552
Tyler Wa Bradshaw *Department of Neurobiology, Duke University School of Medicine, Durham, United States.ORCID 0000-0003-4480-1187
Greg WaittProteomics and Metabolomics Shared Resource, Duke University School of Medicine, Durham, United States.
Erik J SoderblomProteomics and Metabolomics Shared Resource, Duke University School of Medicine, Durham, United States.
Tricia HoProteomics and Metabolomics Shared Resource, Duke University School of Medicine, Durham, United States.
Anna RajabBurjeel Hospital, VPS Healthcare, Muscat, Oman.
Ricardo VanciniDepartment of Pathology, Duke University School of Medicine, Durham, United States.
Il Hwan KimDepartment of Cell Biology, Duke University School of Medicine, Durham, United States.
Scott H SoderlingDepartment of Neurobiology, Duke University School of Medicine, Durham, United States.ORCID 0000-0001-7808-197X
Duke University · USUniversity of Tennessee Health Science Center · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Molecular Analysis of Developmental Brain Disorders Associated with Synaptic PathologyR01MH111684 · NIMH · DUKE UNIVERSITY · PI SCOTT H SODERLING · 2017 to 2026
$6.6M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
New Proteomic and Genome Engineering Approaches to Decipher Astrocyte Function at SynapsesR01DA047258 · NIDA · DUKE UNIVERSITY · PI EROGLU, CAGLA, SODERLING, SCOTT H · 2018 to 2020
$2.1M
Genes, Neural Circuits, and BehaviorR01MH117429 · NIMH · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI KIM, IL HWAN · 2019 to 2022
$1.5M
Genes, Neural Circuits, and BehaviorR56MH117429 · NIMH · DUKE UNIVERSITY · PI KIM, IL HWAN · 2018 to 2018
$400k
Interneuron Synapses: In Vivo Chemicogenetic Proteomics to Discover Developmental Brain Disorder EtiologiesF30MH117851 · NIMH · DUKE UNIVERSITY · PI COURTLAND, JAMIE LYNN · 2019 to 2021
$126k
Interrogating the role of the novel synaptic protein Rogdi in GABAergic inhibition and epilepsyF31NS113738 · NINDS · DUKE UNIVERSITY · PI BRADSHAW, TYLER WESLEY · 2019 to 2020
$70k
Brain and Behavior Research Foundation NARSAD 25163NIDA NIH HHS R01 DA047258NIGMS NIH HHS T32 GM007171NIGMS NIH HHS T32 GM145449NIMH NIH HHS F30 MH117851NIMH NIH HHS R01 MH111684NIMH NIH HHS R01 MH117429NIMH NIH HHS R56 MH117429NINDS NIH HHS F31 NS113738
6 · The paper itself

Abstract

Mutation of the Wiskott-Aldrich syndrome protein and SCAR homology (WASH) complex subunit, SWIP, is implicated in human intellectual disability, but the cellular etiology of this association is unknown. We identify the neuronal WASH complex proteome, revealing a network of endosomal proteins. To uncover how dysfunction of endosomal SWIP leads to disease, we generate a mouse model of the human

Indexed as

AnimalsCognitionEndosomesFemaleHumansIntellectual DisabilityIntracellular Signaling Peptides and ProteinsLysosomesMaleMiceMice, TransgenicMovementMovement DisordersProteomeIntracellular Signaling Peptides and ProteinsProteomeWSB1 protein, humancell biologyendosomehumanlysosomemotor impairmentmouseneuroscienceproteomicsSWIPWASH complex

Identifiers

PMID33749590
PMCPMC7984842
OpenAlexW3139121890

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.