Evidence map›Paper›PMID 38958410›Full record

ReviewDevelopmental dynamics : an official publication of the American Association of Anatomists2024

Actin cytoskeletal regulation of ciliogenesis in development and disease.

Brittany M Hufft-Martinez, Henry H Wang, Irfan Saadi, Pamela V Tran

Abstract readReview
In one paragraph

Review in Developmental dynamics : an official publication of the American Association of Anatomists, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Centrosomal JAK2 Tyrosine Kinase Regulates Primary Cilia Length, Cell Proliferation, and Cilia Orientation During Cell Migration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Loss of Twist1 leads to disruption of ciliary length, endocytic vesicle dynamics, and cell-cell junctions during neural tube formation.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  4. Superoxide dismutase impacts extracellular vesicle biogenesis and uptake.bioRxiv : the preprint server for biology · 2025
    Article
  5. Genetic interaction ofbioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. bioRxiv : the preprint server for biology · 2025
    Article
  9. 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

4 authors.

Brittany M Hufft-MartinezDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, Kansas, USA.ORCID 0000-0002-2063-5420
Henry H WangDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, Kansas, USA.
Irfan SaadiDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, Kansas, USA.ORCID 0000-0002-6250-6651
Pamela V TranDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, Kansas, USA.ORCID 0000-0003-4619-4376

Funding

Role of SPECC1L cytoskeletal protein in palate elevation dynamicsR01DE032825 · NIDCR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Irfan Saadi · 2023 to 2026
$2.4M
Investigating the protective effect of maternal Thm1 heterozygosity against cleft palateR21DE032515 · NIDCR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SAADI, IRFAN, TRAN, PAMELA VIVIAN · 2023 to 2024
$426k
In utero rescue of cleft palate using maternal administration of folic acidR21DE032742 · NIDCR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SAADI, IRFAN, TRAN, PAMELA VIVIAN · 2023 to 2024
$426k
Role of Specc1l in ciliogenesis during craniofacial developmentF31DE031181 · NIDCR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI MARTINEZ, BRITTANY M · 2021 to 2022
$72k
Bionexus KC Patton TrustNIDCR NIH HHS F31 DE031181NIDCR NIH HHS F31 DE31181NIDCR NIH HHS R01 DE032825NIDCR NIH HHS R21 DE032515NIDCR NIH HHS R21 DE032742
6 · The paper itself

Abstract

Primary cilia are antenna-like sensory organelles that are evolutionarily conserved in nearly all modern eukaryotes, from the single-celled green alga, Chlamydomonas reinhardtii, to vertebrates and mammals. Cilia are microtubule-based cellular projections that have adapted to perform a broad range of species-specific functions, from cell motility to detection of light and the transduction of extracellular mechanical and chemical signals. These functions render cilia essential for organismal development and survival. The high conservation of cilia has allowed for discoveries in C. reinhardtii to inform our understanding of the basic biology of mammalian primary cilia, and to provide insight into the genetic etiology of ciliopathies. Over the last two decades, a growing number of studies has revealed that multiple aspects of ciliary homeostasis are regulated by the actin cytoskeleton, including centrosome migration and positioning, vesicle transport to the basal body, ectocytosis, and ciliary-mediated signaling. Here, we review actin regulation of ciliary homeostasis, and highlight conserved and divergent mechanisms in C. reinhardtii and mammalian cells. Further, we compare the disease manifestations of patients with ciliopathies to those with mutations in actin and actin-associated genes, and propose that primary cilia defects caused by genetic alteration of the actin cytoskeleton may underlie certain birth defects.

Indexed as

Actin CytoskeletonCiliaAnimalsChlamydomonas reinhardtiiCiliopathiesHumansactin cytoskeletonbirth defectsChlamydomonasciliamammalsmicrotubules

Identifiers

PMID38958410
PMCPMC11611694

What OpenQuestion holds

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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.