Evidence map›Paper›PMID 30082068›Full record

ArticleCell stem cell2018

Id1 Ablation Protects Hematopoietic Stem Cells from Stress-Induced Exhaustion and Aging.

Satyendra K Singh, Shweta Singh, Stephen Gadomski, Lei Sun, Alexander Pfannenstein, Valentin Magidson, Xiongfong Chen, Serguei Kozlov, Lino Tessarollo, Kimberly D Klarmann and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
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  8. Science advances · 2025
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  12. Review
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  15. The p53 challenge of hematopoietic stem cell gene editing.Molecular therapy. Methods & clinical development · 2023
    Review
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  18. 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

11 authors at 3 institutions in 2 countries.

Satyendra K SinghMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA; Department of Stem Cell and Cell Culture, Center for Advanced Research, King George's Medical University, Lucknow 226003, India.
Shweta SinghMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Stephen GadomskiMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Lei SunMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Alexander PfannensteinMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Valentin MagidsonOptical Microscopy and Analysis Lab, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Xiongfong ChenAdvanced Biomedical and Computation Sciences, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Serguei KozlovCenter for Advanced Preclinical Research, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Lino TessarolloMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Kimberly D KlarmannMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA; Basic Science Program and Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Jonathan R KellerMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA; Basic Science Program and Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA. Electronic address: kellerjo@mail.nih.gov.
Frederick National Laboratory for Cancer Research · USCancer Genetics (United States) · USCenter for Cancer Research · US

Funding

Gene Targeting FacilityZICBC011265 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TESSAROLLO, LINO · 2010 to 2025
$8.9M
Regulation of Hematopoiesis: Gene Therapy PotentialZ01BC010001 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KELLER, JONATHAN R · 1996 to 2008
$2.1M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z01 BC010001NCI NIH HHS HHSN261200800001ENULL Z01 BC010001-12
6 · The paper itself

Abstract

Defining mechanisms that maintain tissue stem cells during homeostasis, stress, and aging is important for improving tissue regeneration and repair and enhancing cancer therapies. Here, we show that Id1 is induced in hematopoietic stem cells (HSCs) by cytokines that promote HSC proliferation and differentiation, suggesting that it functions in stress hematopoiesis. Genetic ablation of Id1 increases HSC self-renewal in serial bone marrow transplantation (BMT) assays, correlating with decreases in HSC proliferation, mitochondrial biogenesis, and reactive oxygen species (ROS) production. Id1

Indexed as

Stress, PhysiologicalAgingAnimalsCells, CulturedHematopoietic Stem CellsInhibitor of Differentiation Protein 1MiceMice, Inbred C57BLMice, KnockoutIdb1 protein, mouseInhibitor of Differentiation Protein 1agingbone marrow transplantationhematopoiesisId proteinsproliferative stressquiescenceself-renewalstem cells

Identifiers

PMID30082068
PMCPMC6149219
OpenAlexW2810071777

What OpenQuestion holds

Textmetadata
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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.