Evidence map›Paper›PMID 31964774›Full record

ArticleDevelopment (Cambridge, England)2020

The ciliary phosphatidylinositol phosphatase Inpp5e plays positive and negative regulatory roles in Shh signaling.

Sandii Constable, Alyssa B Long, Katharine A Floyd, Stéphane Schurmans, Tamara Caspary

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Regulation of INPP5E in Ciliogenesis, Development, and Disease.International journal of biological sciences · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Studying Hedgehog Signaling During Mouse Neural Tube Development.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  13. INPP5E and Coordination of Signaling Networks in Cilia.Frontiers in molecular biosciences · 2022
    Review
  14. Review
  15. Article
  16. Cilia, neural development and disease.Seminars in cell & developmental biology · 2021
    Review
  17. Review
  18. Down-Regulation ofFrontiers in neurology · 2021
    Article
  19. Article
  20. Signaling in the primary cilium through the lens of the Hedgehog pathway.Wiley interdisciplinary reviews. Developmental biology · 2020
    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

5 authors at 2 institutions in 2 countries.

Sandii ConstableDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.ORCID 0000-0002-3809-4976
Alyssa B LongDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.ORCID 0000-0002-4467-4213
Katharine A FloydDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
Stéphane SchurmansLaboratory of Functional Genetics, GIGA-R Centre, Université de Liège, Liège 4000, Belgium.ORCID 0000-0002-5579-3840
Tamara CasparyDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA tcaspar@emory.edu.ORCID 0000-0002-6579-7589
Emory University · USUniversity of Liège · BE

Funding

ENNCF - Viral Vector CoreP30NS055077 · NINDS · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2008 to 2018
$6.8M
Molecular mechanisms of ARF family GTPasesR35GM122568 · NIGMS · EMORY UNIVERSITY · PI KAHN, RICHARD A · 2017 to 2024
$3.7M
The Regulation and Cellular Activities of the ARL2 GTPaseR01GM090158 · NIGMS · EMORY UNIVERSITY · PI KAHN, RICHARD A · 2010 to 2017
$2.5M
Genetic Dissection of Signaling and CiliaR35GM122549 · NIGMS · EMORY UNIVERSITY · PI CASPARY, TAMARA J. · 2017 to 2021
$2.0M
Mechanisms underlying Joubert syndrome related brain malformationsR01NS090029 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ANTON, EVA S, CASPARY, TAMARA J. · 2015 to 2018
$1.9M
Biology of the ARL13B GTPaseR01GM110663 · NIGMS · EMORY UNIVERSITY · PI CASPARY, TAMARA J., KAHN, RICHARD A · 2014 to 2017
$1.7M
NIGMS NIH HHS R01 GM090158NIGMS NIH HHS R01 GM110663NIGMS NIH HHS R35 GM122549NIGMS NIH HHS R35 GM122568NINDS NIH HHS P30 NS055077NINDS NIH HHS R01 NS090029
6 · The paper itself

Abstract

Sonic hedgehog (Shh) signal transduction specifies ventral cell fates in the neural tube and is mediated by the Gli transcription factors that play both activator (GliA) and repressor (GliR) roles. Cilia are essential for Shh signal transduction and the ciliary phosphatidylinositol phosphatase Inpp5e is linked to Shh regulation. In the course of a forward genetic screen for recessive mouse mutants, we identified a functional null allele of inositol polyphosphate-5-phosphatase E (

Indexed as

AllelesAnimalsBody PatterningCiliaEmbryo, MammalianHedgehog ProteinsMiceMice, Inbred C57BLMice, TransgenicNerve Tissue ProteinsNeural TubePhosphoinositide 5-PhosphatasesPhosphoric Monoester HydrolasesSignal TransductionSmoothened ReceptorZinc Finger Protein Gli3Gli3 protein, mouseHedgehog ProteinsNerve Tissue ProteinsPhosphoinositide 5-PhosphatasesPhosphoric Monoester HydrolasesShh protein, mouseSmoothened ReceptorSmo protein, mouseZinc Finger Protein Gli3CiliaInpp5eNeural tube patterningPhosphatidylinositol phosphataseSonic hedgehog

Identifiers

PMID31964774
PMCPMC7033722
OpenAlexW3002577451

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.