Evidence map›Paper›PMID 30728174›Full record

ArticleThe Journal of experimental medicine2019

The developmental stage of the hematopoietic niche regulates lineage in

R Grant Rowe, Edroaldo Lummertz da Rocha, Patricia Sousa, Pavlos Missios, Michael Morse, William Marion, Alena Yermalovich, Jessica Barragan, Ronald Mathieu, Deepak Kumar Jha and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

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  10. The emergence of the stem cell niche.Trends in cell biology · 2023
    Review
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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

13 authors at 1 institution in 1 country.

R Grant RoweStem Cell Program, Boston Children's Hospital, Boston, MA.
Edroaldo Lummertz da RochaStem Cell Program, Boston Children's Hospital, Boston, MA.ORCID 0000-0003-0537-4223
Patricia SousaStem Cell Program, Boston Children's Hospital, Boston, MA.ORCID 0000-0001-6153-9518
Pavlos MissiosStem Cell Program, Boston Children's Hospital, Boston, MA.
Michael MorseStem Cell Program, Boston Children's Hospital, Boston, MA.
William MarionStem Cell Program, Boston Children's Hospital, Boston, MA.
Alena YermalovichStem Cell Program, Boston Children's Hospital, Boston, MA.
Jessica BarraganStem Cell Program, Boston Children's Hospital, Boston, MA.
Ronald MathieuFlow Cytometry Core Facility, Boston Children's Hospital, Boston, MA.ORCID 0000-0002-7625-0239
Deepak Kumar JhaStem Cell Program, Boston Children's Hospital, Boston, MA.
Mark D FlemingHarvard Medical School, Boston, MA.
Trista E NorthStem Cell Program, Boston Children's Hospital, Boston, MA.
George Q DaleyStem Cell Program, Boston Children's Hospital, Boston, MA george.daley@childrens.harvard.edu.ORCID 0000-0002-6346-5919
Boston Children's Hospital · US

Funding

Customized stem cells for clinical application in blood disordersR24DK092760 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI COLLINS, JAMES J, DALEY, GEORGE Q · 2011 to 2018
$10.7M
Stem cells for therapeutics discovery in genetic blood disordersU01HL134812 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI DALEY, GEORGE Q, LIPTON, JEFFREY M · 2016 to 2022
$8.3M
Role of the Lin28b/let-7 axis in the maturation of hematopoietic progenitor cellsK08DK114527 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI ROWE, ROBERT GRANT · 2017 to 2021
$704k
The role of CMTR2 in Lung CancerK00CA212487 · NCI · DANA-FARBER CANCER INST · PI YERMALOVICH, ALENA · 2019 to 2022
$374k
The role of Lin28/let 7 pathway in Wilms' tumorF99CA212487 · NCI · HARVARD UNIVERSITY · PI YERMALOVICH, ALENA · 2016 to 2017
$65k
NCI NIH HHS F99 CA212487NCI NIH HHS K00 CA212487NHLBI NIH HHS U01 HL134812NIDDK NIH HHS K08 DK114527NIDDK NIH HHS R24 DK092760
6 · The paper itself

Abstract

Leukemia phenotypes vary with age of onset. Delineating mechanisms of age specificity in leukemia could improve disease models and uncover new therapeutic approaches. Here, we used heterochronic transplantation of leukemia driven by

Indexed as

AgingAnimalsAnimals, NewbornB-LymphocytesChemokine CCL5FemaleGene Expression Regulation, LeukemicHematopoiesisHematopoietic Stem CellsHistone-Lysine N-MethyltransferaseLeukemiaLeukocyte Common AntigensMaleMice, Inbred C57BLMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionCcl5 protein, mouseChemokine CCL5Histone-Lysine N-MethyltransferaseKmt2a protein, mouseLeukocyte Common AntigensMLL-AF9 fusion protein, mouseMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, Fusion

Identifiers

PMID30728174
PMCPMC6400531
OpenAlexW2914693126

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.