Evidence map›Paper›PMID 8334987›Full record

ArticleThe EMBO journal1993

Murine c-mpl: a member of the hematopoietic growth factor receptor superfamily that transduces a proliferative signal.

R C Skoda, D C Seldin, M K Chiang, C L Peichel, T F Vogt, P Leder

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 172 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  5. Tuning MPL signaling to influence hematopoietic stem cell differentiation and inhibit essential thrombocythemia progenitors.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  6. Review
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  9. Structure of the receptor-binding domain of human thrombopoietin determined by complexation with a neutralizing antibody fragment.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  10. Review
  11. Article
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  19. Article
  20. Identification of a novel pathway important for proliferation and differentiation of primary erythroid progenitors.Proceedings of the National Academy of Sciences of the United States of America · 1997
    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

6 authors at 2 institutions in 1 country.

R C SkodaHoward Hughes Medical Institute, Harvard Medical School, Boston, MA 02115.
D C Seldin
M K Chiang
C L Peichel
T F Vogt
P Leder
Harvard University · USHoward Hughes Medical Institute · US

Funding

IN VITRO AND IN VIVO STUDIES OF THE HUMAN IL-4 RECEPTORK08HL002686 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SELDIN, DAVID C · 1991 to 1996
–
NHLBI NIH HHS 5K08HL02686-02
6 · The paper itself

Abstract

The murine myeloproliferative leukemia virus has previously been shown to contain a fragment of the coding region of the c-mpl gene, a member of the cytokine receptor superfamily. We have isolated cDNA and genomic clones encoding murine c-mpl and localized the c-mpl gene to mouse chromosome 4. Since some members of this superfamily function by transducing a proliferative signal and since the putative ligand of mpl is unknown, we have generated a chimeric receptor to test the functional potential of mpl. The chimera consists of the extracellular domain of the human interleukin-4 receptor and the cytoplasmic domain of mpl. A mouse hematopoietic cell line transfected with this construct proliferates in response to human interleukin-4, thereby demonstrating that the cytoplasmic domain of mpl contains all elements necessary to transmit a growth stimulatory signal. In addition, we show that 25-40% of mpl mRNA found in the spleen corresponds to a novel truncated and potentially soluble isoform of mpl and that both full-length and truncated forms of mpl protein can be immunoprecipitated from lysates of transfected COS cells. Interestingly, however, although the truncated form of the receptor possesses a functional signal sequence and lacks a transmembrane domain, it is not detected in the culture media of transfected cells.

Indexed as

Neoplasm ProteinsReceptors, CytokineSignal TransductionAlternative SplicingAmino Acid SequenceAnimalsBase SequenceCells, CulturedChromosome MappingCloning, MolecularDNAHumansInterleukin-4MiceMice, Inbred C57BLMolecular Sequence DataDNAInterleukin-4MPL protein, humanNeoplasm ProteinsProto-Oncogene ProteinsReceptors, Colony-Stimulating FactorReceptors, CytokineReceptors, ImmunologicReceptors, ThrombopoietinRNA, Messenger

Identifiers

PMID8334987
PMCPMC413511
OpenAlexW125588914

What OpenQuestion holds

Textmetadata
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.