Evidence map›Paper›PMID 37556208›Full record

ArticleMolecular biology of the cell2023

Endoplasmic Reticulum Exit Sites scale with somato-dendritic size in neurons.

Ruben Land, Richard Fetter, Xing Liang, Christopher P Tzeng, Caitlin A Taylor, Kang Shen

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2023. 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. Article
  2. The Neuronal Golgi Network and Its Acolytes.Sub-cellular biochemistry · 2026
    Review
  3. Article
  4. Review
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

6 authors.

Ruben LandDepartment of Biology, Stanford University, Stanford, CA 94305.ORCID 0000-0003-4376-0205
Richard FetterHoward Hughes Medical Institute, Stanford University, Stanford, CA 94305.
Xing LiangDepartment of Biology, Stanford University, Stanford, CA 94305.
Christopher P TzengDepartment of Biology, Stanford University, Stanford, CA 94305.
Caitlin A TaylorDepartment of Biology, Stanford University, Stanford, CA 94305.
Kang ShenDepartment of Biology, Stanford University, Stanford, CA 94305.

Funding

Patterning dendritic branches with environmental and neuronal surface moleculesR01NS082208 · NINDS · STANFORD UNIVERSITY · PI KANG SHEN · 2013 to 2026
$4.1M
NINDS NIH HHS R01 NS082208
6 · The paper itself

Abstract

Nervous systems exhibit dramatic diversity in cell morphology and size. How neurons regulate their biosynthetic and secretory machinery to support such diversity is not well understood. Endoplasmic reticulum exit sites (ERESs) are essential for maintaining secretory flux, and are required for normal dendrite development, but how neurons of different size regulate secretory capacity remains unknown. In

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsAnimalsBiological TransportDendritesEndoplasmic ReticulumSensory Receptor CellsCaenorhabditis elegans Proteins

Identifiers

PMID37556208
PMCPMC10559313

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.