Evidence map›Paper›PMID 32161758›Full record

ArticleFrontiers in cell and developmental biology2020

Notch Dosage

Christopher A Blackwood, Alessandro Bailetti, Sayan Nandi, Thomas Gridley, Jean M Hébert

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Frontiers in neuroscience · 2022
    Article
  4. Article
  5. Biological Significance of NOTCH Signaling Strength.Frontiers in cell and developmental biology · 2021
    Review
  6. Article
  7. 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 4 institutions in 1 country.

Christopher A BlackwoodMolecular Neuropsychiatry Research Branch, National Institutes of Health/National Institute on Drug Abuse Intramural Research Program, Baltimore, MD, United States.
Alessandro BailettiDepartment of Biomedical Sciences, Cornell University, Ithaca, NY, United States.
Sayan NandiDepartments of Neuroscience and Genetics, Albert Einstein College of Medicine, New York, NY, United States.
Thomas GridleyMaine Medical Center Research Institute, Scarborough, ME, United States.
Jean M HébertDepartments of Neuroscience and Genetics, Albert Einstein College of Medicine, New York, NY, United States.
Albert Einstein College of Medicine · USCornell University · USMaine Medical Center Research Institute · USNational Institute on Drug Abuse · US

Funding

Bronx-Einstein Training in Teaching and Research (BETTR), an IRACDA programK12GM102779 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Dianne Cox, Johanna Patricia Daily · 2012 to 2026
$9.2M
Genetic Analysis of Forebrain Patterning & NeurogenesisR01MH070596 · NIMH · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI HEBERT, JEAN M · 2006 to 2017
$3.9M
WNTs, FGFs, and BMPs Induce and Maintain the TelencephalonR01MH083804 · NIMH · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI HEBERT, JEAN M · 2009 to 2013
$2.0M
Regulation of Neurogenesis by Jagged1 in the Embryonic SVZF31DC011709 · NIDCD · CORNELL UNIVERSITY · PI BLACKWOOD, CHRISTOPHER ALEXANDER · 2011 to 2013
$74k
NIDCD NIH HHS F31 DC011709NIGMS NIH HHS K12 GM102779NIMH NIH HHS R01 MH070596NIMH NIH HHS R01 MH083804
6 · The paper itself

Abstract

Neural stem cells in the lateral ganglionic eminence (LGE) generate progenitors that migrate through the rostral migratory stream (RMS) to repopulate olfactory bulb (OB) interneurons, but the regulation of this process is poorly defined. The evolutionarily conserved Notch pathway is essential for neural development and maintenance of neural stem cells. Jagged1, a Notch ligand, is required for stem cell maintenance. In humans, heterozygous mutations in JAGGED1 cause Alagille syndrome, a genetic disorder characterized by complications such as cognitive impairment and reduced number of bile ducts in the liver, suggesting the presence of a JAGGED1 haploinsufficient phenotype. Here, we examine the role of Jagged1 using a conditional loss-of-function allele in the nervous system. We show that heterozygous

Indexed as

Alagille syndromeinterneuronslateral ganglionic eminenceneural stem/progenitor cellsneurogenesisNotcholfactory bulbrostral migratory stream

Identifiers

PMID32161758
PMCPMC7054221
OpenAlexW3008250312

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.