Evidence map›Paper›PMID 32651191›Full record

ArticleLife science alliance2020

Loss of polycystins suppresses deciliation via the activation of the centrosomal integrity pathway.

Vasileios Gerakopoulos, Peter Ngo, Leonidas Tsiokas

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Quinomycin A reduces cyst progression in polycystic kidney disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  12. Intraflagellar Transport Proteins as Regulators of Primary Cilia Length.Frontiers in cell and developmental biology · 2021
    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

3 authors at 1 institution in 1 country.

Vasileios GerakopoulosDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Peter NgoDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Leonidas TsiokasDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA ltsiokas@ouhsc.edu.ORCID 0000-0002-3659-1813
University of Oklahoma Health Sciences Center · US

Funding

Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Wade Williams · 2018 to 2026
$27.1M
TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DHANASEKARAN, DANNY N. · 2012 to 2022
$21.3M
Regulation of Ca++ signaling by the PDK 2 gene productR01DK059599 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TSIOKAS, LEONIDAS · 2002 to 2020
$4.2M
Ciliary Disassembly, a modifier of Autosomal Dominant Polycystic Kidney DiseaseR01DK126705 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TSIOKAS, LEONIDAS · 2021 to 2024
$1.4M
Regulation of calcium signaling by the PKD2 gene productR56DK059599 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TSIOKAS, LEONIDAS · 2010 to 2010
$178k
Ciliary disassembly, a modifier of Polycystic Kidney DiseaseR56DK117654 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TSIOKAS, LEONIDAS · 2018 to 2018
$100k
NCI NIH HHS P30 CA225520NIDDK NIH HHS R01 DK059599NIDDK NIH HHS R01 DK126705NIDDK NIH HHS R56 DK059599NIDDK NIH HHS R56 DK117654NIGMS NIH HHS P20 GM103639
6 · The paper itself

Abstract

The primary cilium is a microtubule-based, antenna-like organelle housing several signaling pathways. It follows a cyclic pattern of assembly and deciliation (disassembly and/or shedding), as cells exit and re-enter the cell cycle, respectively. In general, primary cilia loss leads to kidney cystogenesis. However, in animal models of autosomal dominant polycystic kidney disease, a major disease caused by mutations in the

Indexed as

AnimalsCentrosomeCiliaDisease Models, AnimalFemaleKidneyMaleMiceMice, Inbred C57BLMitosisMutationNIH 3T3 CellsPolycystic Kidney, Autosomal DominantPolycystic Kidney DiseasesSignal TransductionTRPP Cation ChannelsTRPP Cation ChannelsTumor Suppressor p53-Binding Protein 1Tumor Suppressor Protein p53Ubiquitin ThiolesteraseUSP28 protein, mouse

Identifiers

PMID32651191
PMCPMC7368097
OpenAlexW3041693166

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.