Evidence map›Paper›PMID 34314696›Full record

ArticleDevelopmental cell2021

Racing against the clock: How flies regenerate just in time.

Allison M Box, Laura Buttitta

Abstract readComment
PubMed Publisher
In one paragraph

Article in Developmental cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Allison M BoxUniversity of Michigan, Molecular, Cellular, and Developmental Biology, Ann Arbor, MI 48109, USA.
Laura ButtittaUniversity of Michigan, Molecular, Cellular, and Developmental Biology, Ann Arbor, MI 48109, USA. Electronic address: buttitta@umich.edu.

Funding

Chromatin remodeling at cell cycle exitR01GM127367 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BUTTITTA, LAURA A · 2018 to 2022
$1.6M
Identification of a novel progenitor cell population for tissue homeostasis and regeneration of the Drosophila prostateF31HD103430 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BOX, ALLISON · 2020 to 2021
$76k
NICHD NIH HHS F31 HD103430NIGMS NIH HHS R01 GM127367
6 · The paper itself

Abstract

In this issue of Developmental Cell, Cohen et al. show that the Drosophila hindgut is a genetically tractable model for studying tissue regeneration. This tissue exhibits different regeneration strategies at different developmental times, demonstrating that the hindgut developmental clock, not tissue type, dictates the mode and capacity for regeneration.

Indexed as

DrosophilaDrosophila ProteinsAnimalsWound HealingDrosophila Proteins

Identifiers

What OpenQuestion holds

Textmetadata
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.