Evidence map›Paper›PMID 29571613›Full record

ArticleDevelopmental biology2018

Hypomorphic Smo mutant with inefficient ciliary enrichment disrupts the highest level of vertebrate Hedgehog response.

Eduardo D Gigante, Alyssa Bushey Long, Johanna Ben-Ami, Tamara Caspary

Erratum issuedAbstract read
In one paragraph

Article in Developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. A Novel Variant in the Cyto-Tail ofMolecular syndromology · 2024
    Article
  3. Article
  4. Article
  5. Studying Hedgehog Signaling During Mouse Neural Tube Development.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Review
  7. Signaling in the primary cilium through the lens of the Hedgehog pathway.Wiley interdisciplinary reviews. Developmental biology · 2020
    Review
  8. Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Eduardo D GiganteNeuroscience Graduate Program, Emory University, Atlanta, GA 30322, USA; Department of Human Genetics, Emory University, Atlanta, GA 30322, USA. Electronic address: eduardo.gigante@emory.edu.
Alyssa Bushey LongDepartment of Human Genetics, Emory University, Atlanta, GA 30322, USA. Electronic address: abushey@emory.edu.
Johanna Ben-AmiDepartment of Human Genetics, Emory University, Atlanta, GA 30322, USA; Emory College of Arts and Sciences, Emory University, Atlanta, GA 30322, USA. Electronic address: jbenami1@pride.hofstra.edu.
Tamara CasparyDepartment of Human Genetics, Emory University, Atlanta, GA 30322, USA. Electronic address: tcaspar@emory.edu.
Emory University · US

Funding

Large Scale Sequencing and Analysis of GenomesU54HG003067 · NHGRI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GABRIEL, STACEY, LANDER, ERIC S · 2004 to 2015
$568.6M
ENNCF - Viral Vector CoreP30NS055077 · NINDS · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2008 to 2018
$6.8M
Training In Systems And Integrative Biology NeuroscienceT32NS096050 · NINDS · EMORY UNIVERSITY · PI Yoland Smith · 2016 to 2026
$3.9M
Molecular mechanisms of ARF family GTPasesR35GM122568 · NIGMS · EMORY UNIVERSITY · PI KAHN, RICHARD A · 2017 to 2024
$3.7M
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
The role of mouse ARL13B in cell diversification during spinal cord developmentR01NS056380 · NINDS · EMORY UNIVERSITY · PI CASPARY, TAMARA J. · 2007 to 2010
$1.5M
NHGRI NIH HHS U54 HG003067NIGMS NIH HHS R01 GM110663NIGMS NIH HHS R35 GM122549NIGMS NIH HHS R35 GM122568NINDS NIH HHS P30 NS055077NINDS NIH HHS R01 NS056380NINDS NIH HHS R01 NS090029NINDS NIH HHS T32 NS096050
6 · The paper itself

Abstract

Smoothened (Smo) is the essential transducer of Sonic hedgehog (Shh) signaling, which regulates cell fate and proliferation during embryogenesis. We identified a novel mouse mutant, cabbie (cbb), and found that its cause is a missense mutation in Smo. We showed the Smo

Indexed as

AnimalsBody PatterningCell Culture TechniquesCiliaHedgehog ProteinsMiceMutationOrganogenesisReverse Transcriptase Polymerase Chain ReactionSignal TransductionSmoothened ReceptorVertebratesHedgehog ProteinsSmoothened ReceptorSmo protein, mouseMouse developmentPrimary ciliaSmoothenedSonic hedgehog signaling

Identifiers

PMID29571613
PMCPMC5903954
OpenAlexW2789519835

What OpenQuestion holds

Textmetadata
LicenceTDM
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.