Evidence map›Paper›PMID 24155296›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Soluble guanylate cyclase generation of cGMP regulates migration of MGE neurons.

Shyamali Mandal, Amelia Stanco, Emmanuel S Buys, Grigori Enikolopov, John L R Rubenstein

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. CO and NO Coordinate Developmental Neuron Migration.International journal of molecular sciences · 2025
    Article
  2. DLX genes and proteins in mammalian forebrain development.Development (Cambridge, England) · 2024
    Review
  3. Article
  4. Science translational medicine · 2022
    Article
  5. Review
  6. Article
  7. Social Origins of Developmental Risk for Mental and Physical Illness.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Review
  8. Article
  9. Article
  10. Article
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 3 institutions in 1 country.

Shyamali MandalDepartment of Psychiatry, Neuroscience Program and the Nina Ireland Laboratory of Developmental Neurobiology, University of California San Francisco, San Francisco, California 94158-2324, Anesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114, and Cold Spring Harbor Laboratories, Laurel Hollow, New York 11791.
Amelia Stanco
Emmanuel S Buys
Grigori Enikolopov
John L R Rubenstein
University of California, San Francisco · USCold Spring Harbor Laboratory · USMassachusetts General Hospital · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 2003 to 2019
$21.8M
Genetic Control of Basal Telencephalic DevelopmentR01MH081880 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2009 to 2023
$8.1M
Genetic Regulation of Telencephalon DevelopmentR37MH049428 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2008 to 2017
$5.9M
NIDDK NIH HHS P30 DK063720NIMH NIH HHS R01 MH081880NIMH NIH HHS R37 MH049428
6 · The paper itself

Abstract

Here we have provided evidence that nitric oxide-cyclic GMP (NO-cGMP) signaling regulates neurite length and migration of immature neurons derived from the medial ganglionic eminence (MGE). Dlx1/2(-/-) and Lhx6(-/-) mouse mutants, which exhibit MGE interneuron migration defects, have reduced expression of the gene encoding the α subunit of a soluble guanylate cyclase (Gucy1A3). Furthermore, Dlx1/2(-/-) mouse mutants have reduced expression of NO synthase 1 (NOS1). Gucy1A3(-/-) mice have a transient reduction in cortical interneuron number. Pharmacological inhibition of soluble guanylate cyclase and NOS activity rapidly induces neurite retraction of MGE cells in vitro and in slice culture and robustly inhibits cell migration from the MGE and caudal ganglionic eminence. We provide evidence that these cellular phenotypes are mediated by activation of the Rho signaling pathway and inhibition of myosin light chain phosphatase activity.

Indexed as

Cell MovementAnimalsCells, CulturedCyclic GMPGuanylate CyclaseHomeodomain ProteinsInterneuronsLIM-Homeodomain ProteinsMedian EminenceMiceMutationMyosin Light ChainsNerve Tissue ProteinsNeuritesNitric Oxide Synthase Type IReceptors, Cytoplasmic and NuclearCyclic GMPDistal-less homeobox proteinsGuanylate CyclaseGucy1a3 protein, mouseHomeodomain ProteinsLHX6 protein, mouseLIM-Homeodomain ProteinsMyosin Light ChainsNerve Tissue ProteinsNitric Oxide Synthase Type INos1 protein, mouseReceptors, Cytoplasmic and NuclearSoluble Guanylyl CyclaseTranscription Factors

Identifiers

PMID24155296
PMCPMC3866415
OpenAlexW2012966258

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.