Evidence map›Paper›PMID 33122431›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

TAZ/Wnt-β-catenin/c-MYC axis regulates cystogenesis in polycystic kidney disease.

Eun Ji Lee, Eunjeong Seo, Jin Won Kim, Sun Ah Nam, Jong Young Lee, Jaehee Jun, Sumin Oh, Minah Park, Eek-Hoon Jho, Kyung Hyun Yoo and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.3field-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

32 citing papers in PubMed, 52 citations in OpenAlex.

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  9. Vasopressin-Sensitive Aqp2 Regulation Mediated by the TAZ-NR4A1 Axis in Renal Collecting Duct Cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  20. Harnessing mechanobiology for kidney organoid research.Frontiers in cell and developmental biology · 2023
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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

12 authors at 4 institutions in 1 country.

Eun Ji LeeDepartment of Biological Science, Sookmyung Women's University, 04310 Seoul, Republic of Korea.ORCID 0000-0001-7929-1653
Eunjeong SeoCell Death Disease Research Center, College of Medicine, The Catholic University of Korea, 06591 Seoul, Korea.
Jin Won KimCell Death Disease Research Center, College of Medicine, The Catholic University of Korea, 06591 Seoul, Korea.
Sun Ah NamCell Death Disease Research Center, College of Medicine, The Catholic University of Korea, 06591 Seoul, Korea.
Jong Young LeeCell Death Disease Research Center, College of Medicine, The Catholic University of Korea, 06591 Seoul, Korea.
Jaehee JunDepartment of Biological Science, Sookmyung Women's University, 04310 Seoul, Republic of Korea.ORCID 0000-0002-9764-4958
Sumin OhDepartment of Biological Science, Sookmyung Women's University, 04310 Seoul, Republic of Korea.
Minah ParkDepartment of Biological Science, Sookmyung Women's University, 04310 Seoul, Republic of Korea.
Eek-Hoon JhoDepartment of Life Science, University of Seoul, 02504 Seoul, Republic of Korea.ORCID 0000-0003-2414-6234
Kyung Hyun YooDepartment of Biological Science, Sookmyung Women's University, 04310 Seoul, Republic of Korea.
Jong Hoon ParkDepartment of Biological Science, Sookmyung Women's University, 04310 Seoul, Republic of Korea; parkjh@sookmyung.ac.kr drkimyk@catholic.ac.kr.ORCID 0000-0002-8082-0214
Yong Kyun KimCell Death Disease Research Center, College of Medicine, The Catholic University of Korea, 06591 Seoul, Korea; parkjh@sookmyung.ac.kr drkimyk@catholic.ac.kr.ORCID 0000-0002-1871-3549
Sookmyung Women's University · KRCatholic University of Korea · KRThe Catholic University of Korea St. Vincent's Hospital · KRUniversity of Seoul · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal-dominant polycystic kidney disease (ADPKD) is the most common genetic renal disease, primarily caused by germline mutation of

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAxin Proteinbeta CateninCell ProliferationDisease Models, AnimalEpithelial CellsHumansKidneyMiceMice, KnockoutPolycystic Kidney, Autosomal DominantPolycystic Kidney DiseasesProtein Kinase CProto-Oncogene Proteins c-mycTrans-ActivatorsAdaptor Proteins, Signal TransducingAxin1 protein, mouseAxin Proteinbeta CateninMyc protein, mouseProtein Kinase Cprotein kinase DProto-Oncogene Proteins c-mycTrans-ActivatorsTRPP Cation ChannelsWwtr1 protein, mousec-mycpolycystic kidneyTAZ

Identifiers

PMID33122431
PMCPMC7682393
OpenAlexW3097767979

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.