Evidence map›Paper›PMID 8570614›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

A family of transmembrane proteins with homology to the MET-hepatocyte growth factor receptor.

E Maestrini, L Tamagnone, P Longati, O Cremona, M Gulisano, S Bione, F Tamanini, B G Neel, D Toniolo, P M Comoglio

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 169 citations in OpenAlex.

  1. Article
  2. Biallelic variants in Plexin B2 (Journal of medical genetics · 2024
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  3. Article
  4. Review
  5. Divergent roles of Plexin D1 in cancer.Biochimica et biophysica acta. Reviews on cancer · 2019
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Overexpression ofOncology letters · 2015
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

10 authors at 5 institutions in 2 countries.

E MaestriniInstitute of Genetics Biochemistry and Evolution, Consiglio Nazionale delle Ricerche, Pavia, Italy.
L Tamagnone
P Longati
O Cremona
M Gulisano
S Bione
F Tamanini
B G Neel
D Toniolo
P M Comoglio
Candiolo Cancer Institute · ITHarvard University Press · USIRCCS Ospedale San Raffaele · ITSalk Institute for Biological Studies · USUniversity of Turin · IT

Funding

SIGNAL TRANSDUCTION BY NON-TRANSMEMBRANE PTPSR01CA049152 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEEL, BENJAMIN G. · 1989 to 2020
$4.4M
Signal Transduction by Non-transmembrane PTPsR37CA049152 · NCI · UNIVERSITY HEALTH NETWORK · PI NEEL, BENJAMIN G. · 2004 to 2013
$4.0M
NCI NIH HHS CA49152Telethon 271
6 · The paper itself

Abstract

In hunting for unknown genes on the human X chromosome, we identified a cDNA in Xq28 encoding a transmembrane protein (SEX) of 1871 amino acids. SEX shares significant homology with the extracellular domain of the receptors encoded by the oncogenes MET, RON, and SEA [hepatocyte growth factor (HGF) receptor family]. Further screenings of cDNA libraries identified three additional sequences closely related to SEX: these were named SEP, OCT, and NOV and were located on human chromosomes 3p, 1, and 3q, respectively. The proteins encoded by these genes contain large cytoplasmic domains characterized by a distinctive highly conserved sequence (SEX domain). Northern blot analysis revealed different expression of the SEX family of genes in fetal tissues, with SEX, OCT, and NOV predominantly expressed in brain, and SEP expressed at highest levels in kidney. In situ hybridization analysis revealed that SEX has a distinctive pattern of expression in the developing nervous system of the mouse, where it is found in postmitotic neurons from the first stages of neuronal differentiation (9.5 day postcoitus). The SEX protein (220 kDa) is glycosylated and exposed at the cell surface. Unlike the receptors of the HGF family, p220SEX, a MET-SEX chimera or a constitutively dimerized TPR-SEX does not show tyrosine kinase activity. These data define a gene family (SEX family) involved in the development of neural and epithelial tissues, which encodes putative receptors with unexpected enzymatic or binding properties.

Indexed as

Multigene FamilyAmino Acid SequenceAnimalsBase SequenceChromosomes, Human, Pair 3DNA, ComplementaryEpitheliumFetusGene Expression Regulation, DevelopmentalGene LibraryHumansMembrane GlycoproteinsMiceMolecular Sequence DataNerve TissueProto-Oncogene Proteins c-metDNA, ComplementaryMembrane GlycoproteinsPLXNA3 protein, humanProto-Oncogene Proteins c-metReceptor Protein-Tyrosine KinasesReceptors, Cell Surface

Identifiers

PMID8570614
PMCPMC40111
OpenAlexW2013745227

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.