Evidence map›Paper›PMID 26175436›Full record

ArticleMethods in cell biology2015

Centriole biogenesis and function in multiciliated cells.

Siwei Zhang, Brian J Mitchell

Abstract read
In one paragraph

Article in Methods in cell biology, 2015. 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.

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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.

Siwei ZhangDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Brian J MitchellDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.

Funding

Developmental Dynamics of Ciliated EpitheliaR01GM089970 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MITCHELL, BRIAN JOSEPH · 2010 to 2022
$4.4M
NIGMS NIH HHS R01 GM089970
6 · The paper itself

Abstract

The use of Xenopus embryonic skin as a model system for the development of ciliated epithelia is well established. This tissue is comprised of numerous cell types, most notably the multiciliated cells (MCCs) that each contain approximately 150 motile cilia. At the base of each cilium lies the centriole-based structure called the basal body. Centriole biogenesis is typically restricted to two new centrioles per cell cycle, each templating from an existing "mother" centriole. In contrast, MCCs are post-mitotic cells in which the majority of centrioles arise "de novo" without templating from a mother centriole, instead, these centrioles nucleate from an electron-dense structure termed the deuterostome. How centriole number is regulated in these cells and the mechanism by which the deuterosome templates nascent centrioles is still poorly understood. Here, we describe methods for regulating MCC cell fate as well as for visualizing and manipulating centriole biogenesis.

Indexed as

AnimalsCentriolesCiliaEmbryo, NonmammalianSpheroids, CellularXenopus laevisBasal bodyCentrioleCiliaDeuterostomeMulticiliated cellXenopus

Identifiers

PMID26175436
PMCPMC4767327

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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.