Evidence map›Paper›PMID 20926630›Full record

ReviewAmerican journal of physiology. Renal physiology2010

Drosophila provides rapid modeling of renal development, function, and disease.

Julian A T Dow, Michael F Romero

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

58 citing papers in PubMed, 110 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Tau Regulates Endoreplication inmicroPublication biology · 2026
    Article
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  10. Review
  11. Transcriptional and functional motifs defining renal function revealed by single-nucleus RNA sequencing.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Crosstalk betweeniScience · 2021
    Article
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  19. Review
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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 at 2 institutions in 3 countries.

Julian A T DowInstitute of Cell, Molecular, and Systems Biology, College of Medical, Veterinary, and Life Sciences, Univ. of Glasgow, Glasgow G12 8QQ, UK. Julian.Dow@glasgow.ac.uk
Michael F Romero
Mayo Clinic · USUniversity of Glasgow · GB

Funding

Mayo Clinic Urology O'Brien Research CenterP50DK083007 · NIDDK · MAYO CLINIC ROCHESTER · PI LIESKE, JOHN C · 2008 to 2012
$5.3M
Molecular mechanisms of the electrogenic Na+ Bicarbonate Cotransporter (NBCe1)R01EY017732 · NEI · MAYO CLINIC ROCHESTER · PI ROMERO, MICHAEL F. · 2006 to 2010
$1.6M
Biotechnology and Biological Sciences Research Council BB/F010397/1NEI NIH HHS EY017732NIDDK NIH HHS DK083007
6 · The paper itself

Abstract

The evolution of specialized excretory cells is a cornerstone of the metazoan radiation, and the basic tasks performed by Drosophila and human renal systems are similar. The development of the Drosophila renal (Malpighian) tubule is a classic example of branched tubular morphogenesis, allowing study of mesenchymal-to-epithelial transitions, stem cell-mediated regeneration, and the evolution of a glomerular kidney. Tubule function employs conserved transport proteins, such as the Na(+), K(+)-ATPase and V-ATPase, aquaporins, inward rectifier K(+) channels, and organic solute transporters, regulated by cAMP, cGMP, nitric oxide, and calcium. In addition to generation and selective reabsorption of primary urine, the tubule plays roles in metabolism and excretion of xenobiotics, and in innate immunity. The gene expression resource FlyAtlas.org shows that the tubule is an ideal tissue for the modeling of renal diseases, such as nephrolithiasis and Bartter syndrome, or for inborn errors of metabolism. Studies are assisted by uniquely powerful genetic and transgenic resources, the widespread availability of mutant stocks, and low-cost, rapid deployment of new transgenics to allow manipulation of renal function in an organotypic context.

Indexed as

AnimalsAnimals, Genetically ModifiedCiliaDisease Models, AnimalDrosophilaDrosophila ProteinsHumansIon TransportKidneyKidney DiseasesMalpighian TubulesMetabolism, Inborn ErrorsModels, AnimalNephrolithiasisOrganogenesisVacuolar Proton-Translocating ATPasesDrosophila ProteinsVacuolar Proton-Translocating ATPases

Identifiers

PMID20926630
PMCPMC3006309
OpenAlexW2135163881

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.