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Paper · 12688310

High affinity molecules disrupting GRB2 protein complexes as a therapeutic strategy for chronic myelogenous leukaemia.

Feller SM and 2 others. Leuk Lymphoma, 2003. Cited by 20 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. High affinity molecules disrupting GRB2 protein complexes as a therapeutic strategy for chronic myelogenous leukaemia. Papers, record 12688310. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/12688310

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Paper

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

Title
High affinity molecules disrupting GRB2 protein complexes as a therapeutic strategy for chronic myelogenous leukaemia.
PubMed
Journal
Leuk Lymphoma
PubMed
Year
2003
PubMed
Publication types
Journal Article, Review
PubMed
Citations, by iCite
20
iCite
Relative citation ratio, by iCite
0.31
iCite
Revised in PubMed
2019-01-16
PubMed

Authors3

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

OrderAuthorForenameKindORCID iD
1Feller SMStephan M
2Tuchscherer GGabriele
3Voss JJan

Source PubMed

Topics29

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

MeSH termMajor
Adaptor Proteins, Signal TransducingMajor topic
Antineoplastic AgentsMajor topic
Fusion Proteins, bcr-ablMajor topic
Leukemia, Myelogenous, Chronic, BCR-ABL PositiveMajor topic
Neoplasm ProteinsMajor topic
ProteinsMajor topic
Animals
Antineoplastic Combined Chemotherapy Protocols
Benzamides
Drug Design
Enzyme Inhibitors
Fatty Acids, Unsaturated
Forecasting
GRB2 Adaptor Protein
Humans
Imatinib Mesylate
Macromolecular Substances
Mice
Peptide Fragments
Phosphatidylinositol 3-Kinases
Piperazines
Protein Binding
Pyrimidines
Signal Transduction
Son of Sevenless Proteins
Structure-Activity Relationship
Transcription Factors
ras Proteins
src Homology Domains

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 by6

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 20 citations.

PMIDTitleJournalYearIn PapersSource
42,979,455The conformational-condensate code of GRB2: State switching, spatial organization, and therapeutic windows.Acta Pharm Sin B2026https://conductscience.org/library/papers/42979455PubMed
39,175,664GRB2: A dynamic adaptor protein orchestrating cellular signaling in health and disease.Biochem Biophys Rep2024https://conductscience.org/library/papers/39175664PubMed
38,533,261Potential pharmacological mechanisms of tanshinone IIA in the treatment of human neuroblastoma based on network pharmacological and molecular docking Technology.Front Pharmacol2024https://conductscience.org/library/papers/38533261PubMed
30,210,578Insights into the Shc Family of Adaptor Proteins.J Mol Signal2017https://conductscience.org/library/papers/30210578PubMed
21,072,043Inhibition of Grb2 expression demonstrates an important role in BCR-ABL-mediated MAPK activation and transformation of primary human hematopoietic cells.Leukemia2011https://conductscience.org/library/papers/21072043PubMed
18,620,523Grb2 signaling in cell motility and cancer.Expert Opin Ther Targets2008https://conductscience.org/library/papers/18620523PubMed

Genes4

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
ABL125PubTator's text mininghttps://conductscience.org/library/genes/25NCBI Gene
BCR613PubTator's text mininghttps://conductscience.org/library/genes/613NCBI Gene
GRB22,885PubTator's text mininghttps://conductscience.org/library/genes/2885NCBI Gene
XYLT264,132PubTator's text mininghttps://conductscience.org/library/genes/64132NCBI 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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