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Paper · 42383990

Blockade of FGFR1 Trafficking to the Cell Surface Results in the Partial Mistargeting of the Receptor to Peroxisomes.

Działek P and 5 others. FASEB J, 2026. Cited by 0 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Blockade of FGFR1 Trafficking to the Cell Surface Results in the Partial Mistargeting of the Receptor to Peroxisomes. Papers, record 42383990. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42383990

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Paper

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

Title
Blockade of FGFR1 Trafficking to the Cell Surface Results in the Partial Mistargeting of the Receptor to Peroxisomes.
PubMed
Journal
FASEB J
PubMed
Year
2026
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
0
iCite
Revised in PubMed
2026-08-13
PubMed

Authors6

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

OrderAuthorForenameKindORCID iD
1Działek PPaulina
2Chorążewska AAleksandra
3Biaduń MMartyna
4Qiu JJian
5Porębska NNatalia
6Opaliński ŁŁukasz

Source PubMed

Topics9

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

MeSH termMajor
PeroxisomesMajor topic
Receptor, Fibroblast Growth Factor, Type 1Major topic
Cell MembraneMajor topic
Humans
Protein Transport
Animals
Endoplasmic Reticulum
Mitochondria
Glycosylation

Source PubMed

Grants4

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
2019/34/E/NZ3/00014Narodowe Centrum Nauki (NCN)PubMed
FENG.02.02-IP.05-0015Fundacja na rzecz Nauki Polskiej (FNP)PubMed
BPN/BCH/2025/1/00007/U/00001Narodowa Agencja Wymiany Akademickiej (NAWA)PubMed
2026YFE0153800International Science and Technology Innovation Cooperation Key Project of ChinaPubMed

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.

References61

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

OrderPMIDTitleJournalYearIn PapersSource
137,393,834STAMBPL1 promotes the progression of lung adenocarcinoma by inhibiting DHRS2 expression.Transl Oncol2023https://conductscience.org/library/papers/37393834PubMed
220,547,751Mitochondrial Hep27 is a c-Myb target gene that inhibits Mdm2 and stabilizes p53.Mol Cell Biol2010https://conductscience.org/library/papers/20547751PubMed
312,706,718Prediction of peroxisomal targeting signal 1 containing proteins from amino acid sequence.J Mol Biol2003https://conductscience.org/library/papers/12706718PubMed
438,831,455Targeting FGFR for cancer therapy.J Hematol Oncol2024https://conductscience.org/library/papers/38831455PubMed
531,291,971DHRS2 mediates cell growth inhibition induced by Trichothecin in nasopharyngeal carcinoma.J Exp Clin Cancer Res2019https://conductscience.org/library/papers/31291971PubMed
633,652,058Emerging roles of dehydrogenase/reductase member 2 (DHRS2) in the pathology of disease.Eur J Pharmacol2021https://conductscience.org/library/papers/33652058PubMed
730,268,746Yeast peroxisomes: How are they formed and how do they grow?Int J Biochem Cell Biol2018https://conductscience.org/library/papers/30268746PubMed
837,552,037Import and quality control of peroxisomal proteins.J Cell Sci2023https://conductscience.org/library/papers/37552037PubMed
925,760,602The 1.65 Å resolution structure of the complex of AZD4547 with the kinase domain of FGFR1 displays exquisite molecular recognition.Acta Crystallogr D Biol Crystallogr2015https://conductscience.org/library/papers/25760602PubMed
1023,414,306Peroxisome formation and maintenance are dependent on the endoplasmic reticulum.Annu Rev Biochem2013https://conductscience.org/library/papers/23414306PubMed

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.

None in this release.

Genes2

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

GeneNCBI Gene IDLinked byIn GenesSource
DHRS210,202PubTator's text mininghttps://conductscience.org/library/genes/10202NCBI Gene
FGFR12,260PubTator's text mininghttps://conductscience.org/library/genes/2260NCBI 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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