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Paper · 16465403

FGF signaling inhibitor, SPRY4, is evolutionarily conserved target of WNT signaling pathway in progenitor cells.

Katoh Y and 1 other. Int J Mol Med, 2006. Cited by 55 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. FGF signaling inhibitor, SPRY4, is evolutionarily conserved target of WNT signaling pathway in progenitor cells. Papers, record 16465403. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/16465403

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Paper

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

Title
FGF signaling inhibitor, SPRY4, is evolutionarily conserved target of WNT signaling pathway in progenitor cells.
PubMed
Journal
Int J Mol Med
PubMed
Year
2006
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
55
iCite
Relative citation ratio, by iCite
1.11
iCite
Revised in PubMed
2008-11-21
PubMed

Authors2

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

OrderAuthorForenameKindORCID iD
1Katoh YYuriko
2Katoh MMasaru

Source PubMed

Topics23

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

MeSH termMajor
Conserved SequenceMajor topic
Fibroblast Growth FactorsMajor topic
Signal TransductionMajor topic
Stem CellsMajor topic
Wnt ProteinsMajor topic
Amino Acid Sequence
Animals
Base Sequence
Binding Sites
Computational Biology
Genome
Genomics
Humans
Lymphoid Enhancer-Binding Factor 1
Mice
Molecular Sequence Data
Multigene Family
Pan troglodytes
Phylogeny
Promoter Regions, Genetic
RNA, Messenger
Rats
TCF Transcription Factors

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 by27

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 55 citations.

PMIDTitleJournalYearIn PapersSource
42,249,671Exosomal miR-4644 Targets SPRY3 to Promote Proliferation and Invasion of Pancreatic Cancer.Cancer Med2026https://conductscience.org/library/papers/42249671PubMed
40,257,378FGFR2 residence in primary cilia is necessary for epithelial cell signaling.J Cell Biol2025https://conductscience.org/library/papers/40257378PubMed
40,051,360Fibroblast Growth Factors: Roles and Emerging Therapeutic Applications.Curr Drug Targets2025https://conductscience.org/library/papers/40051360PubMed
39,227,612SPRED3 regulates the NF-κB signaling pathway in thyroid cancer and promotes the proliferation.Sci Rep2024https://conductscience.org/library/papers/39227612PubMed
38,895,124Role of long non-coding RNA in inflammatory bowel disease.Front Immunol2024https://conductscience.org/library/papers/38895124PubMed
37,643,784Pan-cancer Analysis Reveals Cancer-dependent Expression of SOX17 and Associated Clinical Outcomes.Cancer Genomics Proteomics2023https://conductscience.org/library/papers/37643784PubMed
36,384,366Sprouty4 is epigenetically upregulated in human colorectal cancer.Epigenetics2023https://conductscience.org/library/papers/36384366PubMed
34,184,730Quantitative analysis of signaling responses during mouse primordial germ cell specification.Biol Open2021https://conductscience.org/library/papers/34184730PubMed
33,445,626Non-Canonical Functions of the ARF Tumor Suppressor in Development and Tumorigenesis.Biomolecules2021https://conductscience.org/library/papers/33445626PubMed
30,082,912FGF18, a prominent player in FGF signaling, promotes gastric tumorigenesis through autocrine manner and is negatively regulated by miR-590-5p.Oncogene2019https://conductscience.org/library/papers/30082912PubMed

1 to 10 of 27

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Genes17

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

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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