Evidence map›Paper›PMID 30291164›Full record

ArticleDevelopment (Cambridge, England)2018

Distinct temporal requirements for Sonic hedgehog signaling in development of the tuberal hypothalamus.

Tanya S Corman, Solsire E Bergendahl, Douglas J Epstein

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

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  15. A Highly ConservedFrontiers in cell and developmental biology · 2021
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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

3 authors at 1 institution in 1 country.

Tanya S CormanDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6145, USA.
Solsire E BergendahlDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6145, USA.ORCID 0000-0002-2449-8822
Douglas J EpsteinDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6145, USA epsteind@pennmedicine.upenn.edu.ORCID 0000-0002-4274-4521
University of Pennsylvania · US

Funding

TRANSCRIPTIONAL CONTROL OF SONIC HEDGEHOG SIGNALINGR01NS039421 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, DOUGLAS J · 2000 to 2023
$8.5M
NINDS NIH HHS R01 NS039421
6 · The paper itself

Abstract

Sonic hedgehog (Shh) plays well characterized roles in brain and spinal cord development, but its functions in the hypothalamus have been more difficult to elucidate owing to the complex neuroanatomy of this brain area. Here, we use fate mapping and conditional deletion models in mice to define requirements for dynamic Shh activity at distinct developmental stages in the tuberal hypothalamus, a brain region with important homeostatic functions. At early time points, Shh signaling regulates dorsoventral patterning, neurogenesis and the size of the ventral midline. Fate-mapping experiments demonstrate that Shh-expressing and -responsive progenitors contribute to distinct neuronal subtypes, accounting for some of the cellular heterogeneity in tuberal hypothalamic nuclei. Conditional deletion of the hedgehog transducer smoothened (Smo), after dorsoventral patterning has been established, reveals that Shh signaling is necessary to maintain proliferation and progenitor identity during peak periods of hypothalamic neurogenesis. We also find that mosaic disruption of

Indexed as

Signal TransductionAnimalsArcuate Nucleus of HypothalamusBody PatterningCell NucleusCell ProliferationEmbryo, MammalianHedgehog ProteinsHypothalamusMiceNeurogenesisNeuronsSmoothened ReceptorTime FactorsZinc Finger Protein GLI1Gli1 protein, mouseHedgehog ProteinsShh protein, mouseSmoothened ReceptorSmo protein, mouseZinc Finger Protein GLI1Cellular heterogeneityDMHShhTuberal hypothalamusVentral midlineVMH

Identifiers

PMID30291164
PMCPMC6240319
OpenAlexW2951166561

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.