Evidence map›Paper›PMID 39293864›Full record

ArticleLife science alliance2024

Ccrk-Mak/Ick signaling is a ciliary transport regulator essential for retinal photoreceptor survival.

Taro Chaya, Yamato Maeda, Ryotaro Tsutsumi, Makoto Ando, Yujie Ma, Naoko Kajimura, Teruyuki Tanaka, Takahisa Furukawa

Abstract read
In one paragraph

Article in Life science alliance, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. The intraflagellar transport cycle.Nature reviews. Molecular cell biology · 2025
    Review
  4. Review
  5. 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

8 authors.

Taro ChayaLaboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, Osaka, Japan.
Yamato MaedaLaboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, Osaka, Japan.
Ryotaro TsutsumiLaboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, Osaka, Japan.
Makoto AndoLaboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, Osaka, Japan.
Yujie MaLaboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, Osaka, Japan.
Naoko KajimuraResearch Center for Ultra-High Voltage Electron Microscopy, Osaka University, Osaka, Japan.ORCID 0000-0002-1546-6239
Teruyuki TanakaDepartment of Developmental Medical Sciences, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Takahisa FurukawaLaboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, Osaka, Japan takahisa.furukawa@protein.osaka-u.ac.jp.ORCID 0000-0003-4171-220X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cilia are microtubule-based sensory organelles whose dysfunction causes ciliopathies in humans. The formation, function, and maintenance of primary cilia depend crucially on intraflagellar transport (IFT); however, the regulatory mechanisms of IFT at ciliary tips are poorly understood. Here, we identified that the ciliopathy kinase Mak is a ciliary tip-localized IFT regulator that cooperatively acts with the ciliopathy kinase Ick, an IFT regulator. Simultaneous disruption of

Indexed as

CiliaSignal TransductionAnimalsBiological TransportCiliopathiesHumansMiceMice, Inbred C57BLMice, KnockoutPhotoreceptor CellsPhotoreceptor Cells, VertebrateProtein Serine-Threonine KinasesRetinaRetinal DegenerationProtein Serine-Threonine Kinases

Identifiers

PMID39293864
PMCPMC11412320

What OpenQuestion holds

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Registered trials

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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.