Evidence map›Paper›PMID 35692423›Full record

ArticleFrontiers in neuroscience2022

Transmembrane Batten Disease Proteins Interact With a Shared Network of Vesicle Sorting Proteins, Impacting Their Synaptic Enrichment.

Mitchell J Rechtzigel, Brandon L Meyerink, Hannah Leppert, Tyler B Johnson, Jacob T Cain, Gavin Ferrandino, Danielle G May, Kyle J Roux, Jon J Brudvig, Jill M Weimer

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Reversible synaptic deficits in early-stage batten disease.Journal of translational medicine · 2026
    Article
  2. Article
  3. Observational
  4. 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

10 authors.

Mitchell J RechtzigelPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Brandon L MeyerinkPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Hannah LeppertPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Tyler B JohnsonPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Jacob T CainPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Gavin FerrandinoPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Danielle G MayPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Kyle J RouxPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Jon J BrudvigPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.
Jill M WeimerPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, SD, United States.

Funding

Yeast 2 HybridP20GM103620 · NIGMS · SANFORD RESEARCH/USD · PI ROUX, KYLE J · 2013 to 2023
$24.2M
The Impact of PD-1 Inhibition on Immune-Response to ChemoradiotherapyP20GM103548 · NIGMS · SANFORD RESEARCH/USD · PI MISKIMINS, W KEITH · 2012 to 2020
$20.8M
Reading Frame Correction for the Treatment of Batten DiseaseR01NS113233 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HASTINGS, MICHELLE L, WEIMER, JILL M · 2020 to 2023
$2.6M
Evolution and application of proximity protein labelingR35GM126949 · NIGMS · SANFORD RESEARCH/USD · PI ROUX, KYLE J · 2018 to 2022
$2.0M
Targeting SMN2 Alternative Splicing for the Treatment of Spinal Muscular AtrophyR01NS069759 · NINDS · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI HASTINGS, MICHELLE L · 2010 to 2014
$1.6M
Correction of Hearing and Vestibular Defects in a Mouse Model for DeafnessR01DC012596 · NIDCD · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI HASTINGS, MICHELLE L · 2013 to 2016
$1.3M
The Identification and Manipulation of RNA Splicing Factor Regulators in Spinal MF31NS076237 · NINDS · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI HAVENS, MALLORY ANN · 2011 to 2013
$86k
NIDCD NIH HHS R01 DC012596NIGMS NIH HHS P20 GM103548NIGMS NIH HHS P20 GM103620NIGMS NIH HHS R35 GM126949NINDS NIH HHS F31 NS076237NINDS NIH HHS R01 NS069759NINDS NIH HHS R01 NS113233
6 · The paper itself

Abstract

Batten disease is unique among lysosomal storage disorders for the early and profound manifestation in the central nervous system, but little is known regarding potential neuron-specific roles for the disease-associated proteins. We demonstrate substantial overlap in the protein interactomes of three transmembrane Batten proteins (CLN3, CLN6, and CLN8), and that their absence leads to synaptic depletion of key partners (i.e., SNAREs and tethers) and altered synaptic SNARE complexing

Indexed as

Batten diseaselysosomeneurodegenerationSNARE (soluble N-ethylmaleimide-sensitive fusion protein attachment protein receptor)vesicle traffic

Identifiers

PMID35692423
PMCPMC9174988

What OpenQuestion holds

Textmetadata
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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.