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Paper · 41520078

Engineered fibroblast growth factor 1 variants uncouple glucose-lowering effects from mitogenic activity with therapeutic potential for type 2 diabetes.

Czyrek AA and 13 others. Mol Biomed, 2026. Cited by 2 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Engineered fibroblast growth factor 1 variants uncouple glucose-lowering effects from mitogenic activity with therapeutic potential for type 2 diabetes. Papers, record 41520078. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41520078

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Paper

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

Title
Engineered fibroblast growth factor 1 variants uncouple glucose-lowering effects from mitogenic activity with therapeutic potential for type 2 diabetes.
PubMed
Journal
Mol Biomed
PubMed
Year
2026
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
2
iCite
Revised in PubMed
2026-06-25
PubMed

Authors14

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

OrderAuthorForenameKindORCID iD
1Czyrek AAAleksandra Ahttps://orcid.org/0000-0002-8518-7075
2Krowarsch DDanielhttps://orcid.org/0000-0003-2856-218X
3Sidor SSzymonhttps://orcid.org/0009-0006-0848-0880
4Janiszewski MMichal
5Drzazga-Wilk EEwa
6Bazydlo-Guzenda KKatarzynahttps://orcid.org/0000-0002-7970-3926
7Buda PPawel
8Pieczykolan JJerzy
9Porebska NNataliahttps://orcid.org/0000-0003-4851-4150
10Minkiewicz MMartahttps://orcid.org/0000-0001-8531-5375

1 to 10 of 14Source PubMed

See all 14 authors

Topics11

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

MeSH termMajor
Diabetes Mellitus, Type 2Major topic
Fibroblast Growth Factor 1Major topic
Protein EngineeringMajor topic
MitogensMajor topic
Hypoglycemic AgentsMajor topic
Animals
Humans
Mice
Cell Proliferation
Blood Glucose
Male

Source PubMed

Grants8

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.

Grant, as the record writes itAgencyCountryNIH projectStated by
POIR.04.01.04.-00-0117/15Narodowe Centrum Badań i RozwojuPubMed
LX22NPO5102Národní ústav pro výzkum rakoviny (CZ)PubMed
LUAUS23295Ministerstvo Školství, Mládeže a TělovýchovyPubMed
GF21-26400KGrantová Agentura České RepublikyPubMed
GF25-15902KGrantová Agentura České RepublikyPubMed
Praemium AcademiaeAkademie Věd České RepublikyPubMed
Weave-Unisono 2024/06/Y/NZ1/00089Narodowe Centrum NaukiPubMed
IDUB 16/2022Ministry of Education and Science, PolandPubMed

Source PubMed

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.

References52

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

OrderPMIDTitleJournalYearIn PapersSource
116,597,617Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family.J Biol Chem2006https://conductscience.org/library/papers/16597617PubMed
226,483,756Endocrine FGFs: Evolution, Physiology, Pathophysiology, and Pharmacotherapy.Front Endocrinol (Lausanne)2015https://conductscience.org/library/papers/26483756PubMed
331,091,809Cross-Talk between Fibroblast Growth Factor Receptors and Other Cell Surface Proteins.Cells2019https://conductscience.org/library/papers/31091809PubMed
415,574,884Phosphorylation-regulated nucleocytoplasmic trafficking of internalized fibroblast growth factor-1.Mol Biol Cell2005https://conductscience.org/library/papers/15574884PubMed
529,983,915A threshold model for receptor tyrosine kinase signaling specificity and cell fate determination.F1000Res2018https://conductscience.org/library/papers/29983915PubMed
636,161,959Autocrine FGF1 signaling promotes glucose uptake in adipocytes.Proc Natl Acad Sci U S A2022https://conductscience.org/library/papers/36161959PubMed
722,522,926A PPARγ-FGF1 axis is required for adaptive adipose remodelling and metabolic homeostasis.Nature2012https://conductscience.org/library/papers/22522926PubMed
814,681,378The Pfam protein families database.Nucleic Acids Res2004https://conductscience.org/library/papers/14681378PubMed
923,403,721Exploring mechanisms of FGF signalling through the lens of structural biology.Nat Rev Mol Cell Biol2013https://conductscience.org/library/papers/23403721PubMed
1019,247,306The FGF family: biology, pathophysiology and therapy.Nat Rev Drug Discov2009https://conductscience.org/library/papers/19247306PubMed

Cited by2

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 2 citations.

PMIDTitleJournalYearIn PapersSource
42,511,911The Role of FGF1 in Chronic Liver Diseases.Biomedicines2026https://conductscience.org/library/papers/42511911PubMed
42,387,574Structure-function relationship in FGF signaling: rational design of highly stable FGF2 variants and their effect on cell growth, metabolism, and survival.J Biol Eng2026https://conductscience.org/library/papers/42387574PubMed

Genes0

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

None in this release.

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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