Evidence map›Paper›PMID 27313231›Full record

ArticleJournal of the American Society of Nephrology : JASN2017

Loss of Cystic Fibrosis Transmembrane Regulator Impairs Intestinal Oxalate Secretion.

Felix Knauf, Robert B Thomson, John F Heneghan, Zhirong Jiang, Adedotun Adebamiro, Claire L Thomson, Christina Barone, John R Asplin, Marie E Egan, Seth L Alper and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Recurrent symptomatic urolithiasis in a patient with cystic fibrosis.Pediatric nephrology (Berlin, Germany) · 2024
    Article
  4. Article
  5. Oxalate secretion is stimulated by a cAMP-dependent pathway in the mouse cecum.Pflugers Archiv : European journal of physiology · 2023
    Article
  6. Review
  7. Role of SLC4 and SLC26 solute carriers during oxidative stress.Acta physiologica (Oxford, England) · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Secondary Oxalate Nephropathy: A Systematic Review.Kidney international reports · 2018
    Article
  16. Article
  17. Review
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Felix KnaufDepartments of Internal Medicine, Felix.Knauf@uk-erlangen.de Peter.Aronson@yale.edu.
Robert B ThomsonDepartments of Internal Medicine.
John F HeneghanDivision of Nephrology and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Zhirong JiangDepartments of Internal Medicine.
Adedotun AdebamiroDepartments of Internal Medicine.
Claire L ThomsonDepartments of Internal Medicine.
Christina BaronePediatrics, and.
John R AsplinLitholink Corporation, Laboratory Corporation of America Holdings, Chicago, Illinois.
Marie E EganPediatrics, and.
Seth L AlperDivision of Nephrology and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Peter S AronsonDepartments of Internal Medicine, Felix.Knauf@uk-erlangen.de Peter.Aronson@yale.edu.
Beth Israel Deaconess Medical Center · USYale University · USFriedrich-Alexander-Universität Erlangen-Nürnberg · DELabCorp (United States) · USPediatrics and Genetics · US

Funding

Renal Physiology and Phenotyping CoreP30DK079310 · NIDDK · YALE UNIVERSITY · PI ARONSON, PETER S. · 2008 to 2022
$16.8M
Roles of SLC26A6 in Renal NaCI Transport and Prevention of Oxalate UrolithiasisR37DK033793 · NIDDK · YALE UNIVERSITY · PI ARONSON, PETER S. · 1994 to 2016
$6.8M
RESEARCH TRAINING IN GASTROENTEROLOGYT32DK007760 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KELLY, CIARAN P · 1999 to 2019
$4.6M
MOLECULAR PHYSIOLOGY OF BAND 3 LIKE PROTEINS OF KIDNEYR37DK043495 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ALPER, SETH LEO · 1998 to 2007
$3.0M
NIDDK NIH HHS P30 DK079310NIDDK NIH HHS R37 DK033793NIDDK NIH HHS R37 DK043495NIDDK NIH HHS T32 DK007760
6 · The paper itself

Abstract

Patients with cystic fibrosis have an increased incidence of hyperoxaluria and calcium oxalate nephrolithiasis. Net intestinal absorption of dietary oxalate results from passive paracellular oxalate absorption as modified by oxalate back secretion mediated by the SLC26A6 oxalate transporter. We used mice deficient in the cystic fibrosis transmembrane conductance regulator gene (Cftr) to test the hypothesis that SLC26A6-mediated oxalate secretion is defective in cystic fibrosis. We mounted isolated intestinal tissue from C57BL/6 (wild-type) and Cftr

Indexed as

AnimalsAntiportersCalcium OxalateCystic Fibrosis Transmembrane Conductance RegulatorHyperoxaluriaIntestinal MucosaMiceMice, KnockoutSulfate TransportersAntiportersCalcium OxalateCystic Fibrosis Transmembrane Conductance RegulatorSlc26a6 protein, mouseSulfate TransportersCell & Transport PhysiologyCystic fibrosiskidney stones

Identifiers

PMID27313231
PMCPMC5198290
OpenAlexW2422348799

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.