Evidence map›Paper›PMID 30733609›Full record

ReviewNature reviews. Nephrology2019

Cellular signalling by primary cilia in development, organ function and disease.

Zeinab Anvarian, Kirk Mykytyn, Saikat Mukhopadhyay, Lotte Bang Pedersen, Søren Tvorup Christensen

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Nephrology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 529 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
529citing papers in PubMed, 1 pooled it
65.9field-weighted citation impact, top 1% 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

529 citing papers in PubMed, 1 synthesis or guideline pooled it, 855 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies.Journal of cell communication and signaling · 2026
    Review
  10. Review
  11. BBS5 as a robust prognostic biomarker in esophageal squamous cell carcinoma: validation in two independent cohorts.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Functions and trafficking mechanisms of RIC-8 inMolecular biology of the cell · 2026
    Article
  18. Article
  19. Article
  20. Article

469 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 2 countries.

Zeinab AnvarianDepartment of Biology, Section of Cell Biology and Physiology, University of Copenhagen, Copenhagen, Denmark.
Kirk MykytynDepartment of Biological Chemistry and Pharmacology, The Ohio State University, Columbus, OH, USA.
Saikat MukhopadhyayDepartment of Cell Biology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-4790-3090
Lotte Bang PedersenDepartment of Biology, Section of Cell Biology and Physiology, University of Copenhagen, Copenhagen, Denmark.
Søren Tvorup ChristensenDepartment of Biology, Section of Cell Biology and Physiology, University of Copenhagen, Copenhagen, Denmark. stchristensen@bio.ku.dk.ORCID http://orcid.org/0000-0001-5004-304X
University of Copenhagen · DKSouthwestern Medical Center · USThe Ohio State University · US

Funding

Signaling at the primary cilium in development and diseaseR01GM113023 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI MUKHOPADHYAY, SAIKAT · 2015 to 2019
$1.4M
Neuronal primary cilia in dopamine receptor 1 signalingR21MH107021 · NIMH · OHIO STATE UNIVERSITY · PI MYKYTYN, KIRK A · 2015 to 2016
$424k
NIGMS NIH HHS R01 GM113023NIMH NIH HHS R21 MH107021
6 · The paper itself

Abstract

Primary cilia project in a single copy from the surface of most vertebrate cell types; they detect and transmit extracellular cues to regulate diverse cellular processes during development and to maintain tissue homeostasis. The sensory capacity of primary cilia relies on the coordinated trafficking and temporal localization of specific receptors and associated signal transduction modules in the cilium. The canonical Hedgehog (HH) pathway, for example, is a bona fide ciliary signalling system that regulates cell fate and self-renewal in development and tissue homeostasis. Specific receptors and associated signal transduction proteins can also localize to primary cilia in a cell type-dependent manner; available evidence suggests that the ciliary constellation of these proteins can temporally change to allow the cell to adapt to specific developmental and homeostatic cues. Consistent with important roles for primary cilia in signalling, mutations that lead to their dysfunction underlie a pleiotropic group of diseases and syndromic disorders termed ciliopathies, which affect many different tissues and organs of the body. In this Review, we highlight central mechanisms by which primary cilia coordinate HH, G protein-coupled receptor, WNT, receptor tyrosine kinase and transforming growth factor-β (TGFβ)/bone morphogenetic protein (BMP) signalling and illustrate how defects in the balanced output of ciliary signalling events are coupled to developmental disorders and disease progression.

Indexed as

OrganogenesisCell DifferentiationCell MovementCiliaCiliary Motility DisordersHedgehog ProteinsHomeostasisHumansSignal TransductionHedgehog Proteins

Identifiers

PMID30733609
PMCPMC6426138
OpenAlexW2913985590

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.