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Paper · 42967007

Change-of-function fibroblast growth factor receptor 3 mutations causing skeletal dysplasias.

Roy T and 4 others. J Cell Commun Signal, 2026.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Change-of-function fibroblast growth factor receptor 3 mutations causing skeletal dysplasias. Papers, record 42967007. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42967007

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Paper

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

Title
Change-of-function fibroblast growth factor receptor 3 mutations causing skeletal dysplasias.
Journal
J Cell Commun Signal
Year
2026
Publication types
Journal Article
Revised in PubMed
2026-11-02

Source PubMed

Authors5

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

OrderAuthorForenameKindORCID iD
1Roy TTanaya
2Feketova ZZuzanahttps://orcid.org/0000-0003-4620-4634
3Liu JJiaweihttps://orcid.org/0009-0000-6917-3100
4Krejci PPavelhttps://orcid.org/0000-0003-0618-9134
5Hristova KKalinahttps://orcid.org/0000-0003-4274-4406

Source PubMed

Topics0

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Grants0

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Trials0

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Comments and corrections0

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References54

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

OrderPMIDTitleJournalYearIn PapersSource
110,490,103Structural basis for FGF receptor dimerization and activation.Cell1999https://conductscience.org/library/papers/10490103PubMed
226,075,305FGFR3 biology and skeletal disease.Connect Tissue Res2015https://conductscience.org/library/papers/26075305PubMed
38,622,701Identification of six novel autophosphorylation sites on fibroblast growth factor receptor 1 and elucidation of their importance in receptor activation and signal transduction.Mol Cell Biol1996https://conductscience.org/library/papers/8622701PubMed
47,719,345Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.Nat Genet1995https://conductscience.org/library/papers/7719345PubMed
522,045,636Sixteen years and counting: the current understanding of fibroblast growth factor receptor 3 (FGFR3) signaling in skeletal dysplasias.Hum Mutat2012https://conductscience.org/library/papers/22045636PubMed
621,030,484Functional selectivity and biased receptor signaling.J Pharmacol Exp Ther2011https://conductscience.org/library/papers/21030484PubMed
77,987,400Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.Nat Genet1994https://conductscience.org/library/papers/7987400PubMed
89,438,390Constitutive activation of fibroblast growth factor receptor 3 by mutations responsible for the lethal skeletal dysplasia thanatophoric dysplasia type I.Cell Growth Differ1998https://conductscience.org/library/papers/9438390PubMed
915,863,030Cellular signaling by fibroblast growth factor receptors.Cytokine Growth Factor Rev2005https://conductscience.org/library/papers/15863030PubMed
1040,821,249Vosoritide (Voxzogo) for Achondroplasia: A Review of Clinical and Real-World Evidence.Cureus2025https://conductscience.org/library/papers/40821249PubMed

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Cited by0

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Genes0

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None in this release.

Drugs0

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None in this release.

Data0

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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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