Evidence map›Paper›PMID 30018091›Full record

ArticleThe Journal of cell biology2018

Non-canonical Ret signaling augments p75-mediated cell death in developing sympathetic neurons.

Christopher R Donnelly, Nicole A Gabreski, Esther B Suh, Monzurul Chowdhury, Brian A Pierchala

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. p75NTRCell proliferation · 2020
    Article
  8. 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 1 institution in 1 country.

Christopher R DonnellyDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI.
Nicole A GabreskiDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI.
Esther B SuhDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI.
Monzurul ChowdhuryDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI.
Brian A PierchalaDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI pierchal@umich.edu.ORCID 0000-0002-9844-1706
University of Michigan · US

Funding

Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Growth factors in the development and physiology of geniculate taste neuronsR01DC015799 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Brian Anthony Pierchala · 2017 to 2026
$4.8M
A p75/Ret Receptor Complex as an Integrator of Survival and DeathR01NS089585 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIERCHALA, BRIAN ANTHONY · 2015 to 2024
$3.9M
Understanding the Function of GFL-Ret Signaling in the Development of the PeripheF30DE023479 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DONNELLY, CHRISTOPHER RYAN · 2014 to 2017
$189k
NIDCD NIH HHS R01 DC015799NIDCR NIH HHS F30 DE023479NIDCR NIH HHS T32 DE007057NIGMS NIH HHS T32 GM007315NINDS NIH HHS R01 NS089585
6 · The paper itself

Abstract

Programmed cell death (PCD) is an evolutionarily conserved process critical in sculpting many organ systems, yet the underlying mechanisms remain poorly understood. Here, we investigated the interactions of pro-survival and pro-apoptotic receptors in PCD using the sympathetic nervous system as a model. We demonstrate that Ret, a receptor tyrosine kinase required for the survival of many neuronal populations, is restricted to a subset of degenerating neurons that rapidly undergo apoptosis. Pro-apoptotic conditions induce Ret to associate with the death receptor p75. Genetic deletion of p75 within Ret

Indexed as

3T3 CellsAnimalsApoptosisCell LineCell SurvivalMiceMice, Inbred C57BLMice, KnockoutNerve Growth FactorNeuronsProto-Oncogene Proteins c-retReceptors, Nerve Growth FactorReceptor, trkASignal TransductionSympathetic Nervous SystemUbiquitinationNerve Growth FactorNgfr protein, mouseProto-Oncogene Proteins c-retReceptors, Nerve Growth FactorReceptor, trkARet protein, mouse

Identifiers

PMID30018091
PMCPMC6122988
OpenAlexW2884802880

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.