Evidence map›Paper›PMID 10023687›Full record

ArticleOncogene1999

Diverse developing mouse lineages exhibit high-level c-Myb expression in immature cells and loss of expression upon differentiation.

K C Ess, D P Witte, C P Bascomb, B J Aronow

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

25 citing papers in PubMed, 58 citations in OpenAlex.

  1. HemaSphere · 2024
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  6. Transcription regulation ofAnnals of translational medicine · 2018
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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

4 authors at 3 institutions in 1 country.

K C EssDivision of Molecular and Developmental Biology Children's Hospital Research Foundation, University of Cincinnati, Ohio 45229, USA.
D P Witte
C P Bascomb
B J Aronow
Cincinnati Children's Hospital Medical Center · USMiami Valley Hospital · USUniversity of Cincinnati · US

Funding

CONTROL OF PURINE CATABOLISM IN THE THYMUSR01DK047022 · NIDDK · CHILDREN'S HOSPITAL MED CTR (CINCINNATI) · PI ARONOW, BRUCE J. · 1994 to 1997
–
NHLBI NIH HHS HL07527NIDDK NIH HHS DK47022
6 · The paper itself

Abstract

The c-myb gene encodes a sequence specific transactivator that is required for fetal hematopoiesis, but its potential role in other tissues is less clear because of the early fetal demise of mice with targeted deletions of the c-myb gene and incomplete of knowledge about c-myb's expression pattern. In the hematopoietic system, c-Myb protein acts on target genes whose expression is restricted to individual lineages, despite Myb's presence and role in multiple immature lineages. This suggests that c-Myb actions within different cell type-specific contexts are strongly affected by combinatorial interactions. To consider the possibility of similar c-Myb actions could extend into non-hematopoietic systems in other cell and tissue compartments, we characterized c-myb expression in developing and adult mice using in situ hybridization and correlated this with stage-specific differentiation and mitotic activity. Diverse tissues exhibited strong c-myb expression during development, notably tooth buds, the thyroid primordium, developing trachea and proximal branching airway epithelium, hair follicles, hematopoietic cells, and gastrointestinal crypt epithelial cells. The latter three of these all maintained high expression into adulthood, but with characteristic restriction to immature cell lineages prior to their terminal differentiation. In all sites, during fetal and adult stages, loss of c-Myb expression correlated strikingly with the initiation of terminal differentiation, but not the loss of mitotic activity. Based on these data, we hypothesize that c-Myb's function during cellular differentiation is both an activator of immature gene expression and a suppressor of terminal differentiation in diverse lineages.

Indexed as

OncogenesAge FactorsAnimalsCell DifferentiationDigestive SystemEmbryonic and Fetal DevelopmentHair FollicleIn Situ HybridizationLiverMiceMitosisOdontogenesisProto-Oncogene ProteinsProto-Oncogene Proteins c-mybThymus GlandThyroid GlandProto-Oncogene ProteinsProto-Oncogene Proteins c-mybTrans-Activators

Identifiers

PMID10023687
OpenAlexW2335608451

What OpenQuestion holds

Texttitle and abstract
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.