Paper · 7094017

A cellular protein is immunologically crossreactive with and functionally homologous to the Fujinami sarcoma virus transforming protein.

Mathey-Prevot B and 2 others. Cell, 1982. Cited by 112 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. A cellular protein is immunologically crossreactive with and functionally homologous to the Fujinami sarcoma virus transforming protein. Papers, record 7094017. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/7094017

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: A cellular protein is immunologically crossreactive with and functionally homologous to the Fujinami sarcoma virus transforming protein.; PubMed
Journal: Cell; PubMed
Year: 1982; PubMed
Publication types: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/7094017/; PubMed
DOI: https://doi.org/10.1016/0092-8674(82)90069-1; PubMed
The journal: https://conductscience.org/library/journal-index/0413066; PubMed
Citations, by iCite: 112; iCite
Relative citation ratio, by iCite: 2.09; iCite
Revised in PubMed: 2019-07-05; PubMed

Authors3

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename
1	Mathey-Prevot B	B
2	Hanafusa H	H
3	Kawai S	S

Source PubMed

Topics12

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
Cell Transformation, Viral	Major topic
Phosphoproteins	Major topic
Viral Proteins	Major topic
Animals
Bone Marrow
Chick Embryo
Cross Reactions
Oncogenic Viruses
Protein Kinases
Proteins
Rats
Tissue Distribution

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References0

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

None in this release.

Cited by41

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 112 citations.

PMID	Title	Journal	Year	In Papers	Source
11,865,067	Activated Fes protein tyrosine kinase induces terminal macrophage differentiation of myeloid progenitors (U937 cells) and activation of the transcription factor PU.1.	Mol Cell Biol	2002	https://conductscience.org/library/papers/11865067	PubMed
8,052,235	Meiosis-dependent tyrosine phosphorylation of a yeast protein related to the mouse p51ferT.	Mol Gen Genet	1994	https://conductscience.org/library/papers/8052235	PubMed
7,523,858	The Fps/Fes protein-tyrosine kinase promotes angiogenesis in transgenic mice.	Mol Cell Biol	1994	https://conductscience.org/library/papers/7523858	PubMed
6,605,429	A fps gene without gag gene sequences transforms cells in culture and induces tumors in chickens.	J Virol	1983	https://conductscience.org/library/papers/6605429	PubMed
6,573,668	Tyrosyl protein kinases in normal rat liver: identification and partial characterization.	Proc Natl Acad Sci U S A	1983	https://conductscience.org/library/papers/6573668	PubMed
6,572,383	Antibodies of predetermined specificity detect two retroviral oncogene products and inhibit their kinase activities.	Proc Natl Acad Sci U S A	1983	https://conductscience.org/library/papers/6572383	PubMed
6,543,243	Characterization of the protein apparently responsible for the elevated tyrosine protein kinase activity in LSTRA cells.	Mol Cell Biol	1984	https://conductscience.org/library/papers/6543243	PubMed
6,328,022	Molecular cloning and characterization of avian sarcoma virus UR2 and comparison of its transforming sequence with those of other avian sarcoma viruses.	J Virol	1984	https://conductscience.org/library/papers/6328022	PubMed
6,323,733	Revertants and partial transformants of rat fibroblasts infected with Fujinami sarcoma virus.	J Virol	1984	https://conductscience.org/library/papers/6323733	PubMed
6,308,423	Transcription of c-onc genes c-rasKi and c-fms during mouse development.	Mol Cell Biol	1983	https://conductscience.org/library/papers/6308423	PubMed

1 to 10 of 41

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Genes1

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes
SRCIN1	80,725	PubTator's text mining	https://conductscience.org/library/genes/80725

Source NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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