Evidence map›Paper›PMID 29263159›Full record

ArticleJournal of the American Society of Nephrology : JASN2018

Pathogenicity of a Human Laminin

Steven D Funk, Raymond H Bayer, Andrew F Malone, Karen K McKee, Peter D Yurchenco, Jeffrey H Miner

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  7. Laminin N-terminus α31 expression during development is lethal and causes widespread tissue-specific defects in a transgenic mouse model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
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  19. Endothelial cell-specific collagen type IV-αAmerican journal of physiology. Renal physiology · 2019
    Article
  20. Review
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

6 authors at 2 institutions in 1 country.

Steven D FunkDivision of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri and.
Raymond H BayerDivision of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri and.
Andrew F MaloneDivision of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri and.
Karen K McKeeDepartment of Pathology and Laboratory Medicine, Robert Wood Johnson Medical School, Rutgers University, Piscataway, New Jersey.
Peter D YurchencoDepartment of Pathology and Laboratory Medicine, Robert Wood Johnson Medical School, Rutgers University, Piscataway, New Jersey.
Jeffrey H MinerDivision of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri and minerj@wustl.edu.
Washington University in St. Louis · USJohnson University · US

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Jeffrey Wade Brown · 2000 to 2026
$30.8M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
LAMININS AND GLOMERULAR FILTRATIONR01DK078314 · NIDDK · WASHINGTON UNIVERSITY · PI MINER, JEFFREY H · 2008 to 2021
$5.4M
RENAL DISEASET32DK007126 · NIDDK · WASHINGTON UNIVERSITY · PI HUMPHREYS, BENJAMIN D. · 1986 to 2022
$5.2M
BASEMENT MEMBRANE SELF-ASSEMBLY &STRUCTURER01DK036425 · NIDDK · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI YURCHENCO, PETER DANA · 1986 to 2022
$4.3M
NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK052574NIDDK NIH HHS R01 DK036425NIDDK NIH HHS R01 DK078314NIDDK NIH HHS T32 DK007126
6 · The paper itself

Abstract

Pierson syndrome is a congenital nephrotic syndrome with eye and neurologic defects caused by mutations in laminin

Indexed as

Abnormalities, MultipleAnimalsAutoantigensCollagen Type IVDisease Models, AnimalDisease ProgressionEye AbnormalitiesFemaleGlomerular Basement MembraneHumansKidney Failure, ChronicLamininMiceMice, TransgenicMutation, MissenseMyasthenic Syndromes, CongenitalAutoantigensCol4a5 protein, mouseCollagen Type IVLamininlaminin beta2type IV collagen alpha3 chainAlport syndromeglomerular basement membranelamininnephrotic syndrome

Identifiers

PMID29263159
PMCPMC5827610
OpenAlexW2781260670

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.