Evidence map›Paper›PMID 29676801›Full record

ArticleThe Journal of physiology2018

Prolonged prenatal hypoxia selectively disrupts collecting duct patterning and postnatal function in male mouse offspring.

Sarah L Walton, Reetu R Singh, Melissa H Little, Josephine Bowles, Joan Li, Karen M Moritz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  7. COVID-19 During Development: A Matter of Concern.Frontiers in cell and developmental biology · 2021
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  9. Deletion of hypoxia-responsive microRNA-210 results in a sex-specific decrease in nephron number.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Sarah L WaltonSchool of Biomedical Sciences, The University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0002-8099-0272
Reetu R SinghDepartment of Physiology, Monash University, Melbourne, VIC, Australia.
Melissa H LittleMurdoch Childrens Research Institute, Parkville, VIC, Australia.
Josephine BowlesSchool of Biomedical Sciences, The University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0003-2867-7438
Joan LiAustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD, Australia.
Karen M MoritzSchool of Biomedical Sciences, The University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0002-0471-8517
The University of Queensland · AUMonash University · AUThe University of Melbourne · AU

Funding

Australian Postgraduate AwardDepartment of Health, Australian Government | National Health and Medical Research Council (NHMRC) APP1009338
6 · The paper itself

Abstract

key pointsIn the present study, we investigated whether hypoxia during late pregnancy impairs kidney development in mouse offspring, and also whether this has long-lasting consequences affecting kidney function in adulthood. Hypoxia disrupted growth of the kidney, particularly the collecting duct network, in juvenile male offspring. By mid-late adulthood, these mice developed early signs of kidney disease, notably a compromised response to water deprivation. Female offspring showed no obvious signs of impaired kidney development and did not develop kidney disease, suggesting an underlying protection mechanism from the hypoxia insult. These results help us better understand the long-lasting impact of gestational hypoxia on kidney development and the increased risk of chronic kidney disease. ABSTRACT: Prenatal hypoxia is a common perturbation to arise during pregnancy, and can lead to adverse health outcomes in later life. The long-lasting impact of prenatal hypoxia on postnatal kidney development and maturation of the renal tubules, particularly the collecting duct system, is relatively unknown. In the present study, we used a model of moderate chronic maternal hypoxia throughout late gestation (12% O

Indexed as

AnimalsAnimals, NewbornFemaleFetal HypoxiaKidney Tubules, CollectingMaleMiceMice, TransgenicPregnancySex Factorscollecting ductfetal hypoxiakidney developement

Identifiers

PMID29676801
PMCPMC6265544
OpenAlexW2891625753

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.