Evidence map›Paper›PMID 40716173›Full record

ReviewSeminars in cell & developmental biology2025

C. elegans: An elegant experimental system for the study of cilia biology.

Inna Nechipurenko, Piali Sengupta

Abstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2025. 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. Functions and trafficking mechanisms of RIC-8 inMolecular biology of the cell · 2026
    Article
  2. The extracellular matrix genebioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Complement Factor H and itsbioRxiv : the preprint server for biology · 2025
    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

2 authors.

Inna NechipurenkoDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, USA. Electronic address: inechipurenko@wpi.edu.
Piali SenguptaDepartment of Biology, Brandeis University, Waltham, MA, USA. Electronic address: sengupta@brandeis.edu.

Funding

Mechanisms of sensory neuron morphological diversification, signaling, and functional plasticityR35GM122463 · NIGMS · BRANDEIS UNIVERSITY · PI Piali Sengupta · 2017 to 2026
$7.7M
Genetic analysis of signaling pathways in cilia assembly and remodelingR35GM155316 · NIGMS · WORCESTER POLYTECHNIC INSTITUTE · PI Inna Nechipurenko · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM122463NIGMS NIH HHS R35 GM155316
6 · The paper itself

Abstract

Caenorhabditis elegans is a genetically tractable organism that has become one of the leading in vivo models for cilia research. Cilia are not required for viability in C. elegans, as only a subset of sensory neurons is ciliated in this organism. Yet, C. elegans cilia exhibit remarkable structural and functional diversity akin to their mammalian counterparts. Since the core mechanisms of cilia assembly are evolutionarily conserved, research in C. elegans has informed studies in other organisms on cilia biogenesis, trafficking, and functions and has provided key insights into mechanisms of cilia dysfunction in human disorders. Here, we provide a general overview of the C. elegans model for cilia research. Specifically, we review different cilia types and their underlying ultrastructural organization, discuss trafficking mechanisms for ciliary proteins, describe emerging functions of ciliary extracellular vesicles, and highlight a broad swathe of sophisticated tools available in C. elegans for studying multiple aspects of cilia biology.

Indexed as

Caenorhabditis elegansCiliaAnimalsCaenorhabditis elegans ProteinsHumansCaenorhabditis elegans ProteinsC. elegansCiliaExtracellular vesiclesIntraflagellar transportSensory

Identifiers

PMID40716173
PMCPMC12820946

What OpenQuestion holds

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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.