Evidence map›Paper›PMID 32675303›Full record

ArticleJournal of the American Society of Nephrology : JASN2020

Kidney Disease-Associated

Somenath Datta, Rama Kataria, Jia-Yue Zhang, Savannah Moore, Kaitlyn Petitpas, Adam Mohamed, Nathan Zahler, Martin R Pollak, Opeyemi A Olabisi

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Evasive mechanisms of human VSG and PfEMP1 antigens with link to Vaccine scenario: a review.Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2025
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Novel Therapies inKidney international reports · 2023
    Review
  19. Article
  20. Article
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

9 authors at 2 institutions in 1 country.

Somenath DattaDivision of Nephrology and Duke Molecular Physiology Institute, Duke University, Durham, North Carolina.
Rama KatariaDivision of Nephrology, Massachusetts General Hospital, Boston, Massachusetts.
Jia-Yue ZhangHarvard Medical School, Boston, Massachusetts.
Savannah MooreDivision of Nephrology, Massachusetts General Hospital, Boston, Massachusetts.
Kaitlyn PetitpasDivision of Nephrology, Massachusetts General Hospital, Boston, Massachusetts.
Adam MohamedDivision of Nephrology, Massachusetts General Hospital, Boston, Massachusetts.
Nathan ZahlerIcagen Inc, Durham, North Carolina.ORCID 0000-0003-0432-2608
Martin R PollakHarvard Medical School, Boston, Massachusetts.
Opeyemi A OlabisiDivision of Nephrology and Duke Molecular Physiology Institute, Duke University, Durham, North Carolina Opeyemi.olabisi@duke.edu.
Harvard University · USBeth Israel Deaconess Medical Center · US

Funding

APOL1 variants: Understanding the basis of disparities in rates of kidney diseaseR01MD007092 · NIMHD · BETH ISRAEL DEACONESS MEDICAL CENTER · PI FRIEDMAN, DAVID J, POLLAK, MARTIN R. · 2012 to 2021
$4.3M
JAK-STAT Inhibition to Reduce Racial Disparities in Kidney DiseaseR01MD016401 · NIMHD · DUKE UNIVERSITY · PI OLABISI, OPEYEMI AYODEJI · 2021 to 2025
$3.5M
A Human Stem Cell-Derived Podocyte Model for APOL1 NephropathyDP2DK124891 · NIDDK · DUKE UNIVERSITY · PI OLABISI, OPEYEMI AYODEJI · 2019 to 2019
$2.4M
APOL1 Nephropathy: Linking Genetics and MechanismsR01MD014726 · NIMHD · BETH ISRAEL DEACONESS MEDICAL CENTER · PI FRIEDMAN, DAVID J, POLLAK, MARTIN R. · 2020 to 2024
$2.4M
NIDDK NIH HHS DP2 DK124891NIMHD NIH HHS R01 MD007092NIMHD NIH HHS R01 MD014726NIMHD NIH HHS R01 MD016401
6 · The paper itself

Abstract

backgroundTwo coding renal risk variants (RRVs) of the

methodsWe generated tetracycline-inducible

resultsAt moderate expression, RRVs but not G0 caused cytotoxicity in a dose-dependent manner that coexpression of G0 did not reduce. RRVs also have dominant effects on canonical pathways relevant for the cellular stress response.

conclusionsIn HEK293 cells, RRVs exhibit a dominant toxic gain-of-function phenotype that worsens with increasing expression. These observations suggest that high steady-state levels of RRVs may underlie cellular injury in

Indexed as

Apolipoprotein L1Cell SurvivalEnergy MetabolismGene Expression ProfilingGenetic VariationHEK293 CellsHumansp38 Mitogen-Activated Protein KinasesPotassiumProtein BiosynthesisProtein Serine-Threonine KinasesAPOL1 protein, humanApolipoprotein L1eIF2alpha kinase, mousep38 Mitogen-Activated Protein KinasesPotassiumProtein Serine-Threonine KinasesAfrican AmericansAPOL1CKDCytotoxicityFSGSGain of function mutation

Identifiers

PMID32675303
PMCPMC7461666
OpenAlexW3043084614

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.