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Paper · 20161828

Cellular Ser/Thr-kinase assays using generic peptide substrates.

Adams DG and 14 others. Curr Chem Genomics, 2008. Cited by 4 papers, by iCite.

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ConductScience Library. Cellular Ser/Thr-kinase assays using generic peptide substrates. Papers, record 20161828. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/20161828

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Paper

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

Title
Cellular Ser/Thr-kinase assays using generic peptide substrates.
PubMed
Journal
Curr Chem Genomics
PubMed
Year
2008
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
4
iCite
Relative citation ratio, by iCite
0.1
iCite
Revised in PubMed
2021-10-20
PubMed

Authors15

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

OrderAuthorForenameKindORCID iD
1Adams DGDeanna G
2Wang YYu
3Mak PAPuiying A
4Chyba JJason
5Shalizi OOrzala
6Matzen JJason
7Anderson PPaul
8Smith TRTim R
9Garcia MMichael
10Welch GLGenevieve L

1 to 10 of 15Source PubMed

See all 15 authors

Topics0

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

None in this release.

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.

References38

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

OrderPMIDTitleJournalYearIn PapersSource
116,407,412Identification of novel in vivo Raf-1 phosphorylation sites mediating positive feedback Raf-1 regulation by extracellular signal-regulated kinase.Mol Biol Cell2006https://conductscience.org/library/papers/16407412PubMed
28,106,507A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002).J Biol Chem1994https://conductscience.org/library/papers/8106507PubMed
312,469,133A general method for the covalent labeling of fusion proteins with small molecules in vivo.Nat Biotechnol2003https://conductscience.org/library/papers/12469133PubMed
415,226,507Labeling of fusion proteins with synthetic fluorophores in live cells.Proc Natl Acad Sci U S A2004https://conductscience.org/library/papers/15226507PubMed
516,864,780Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries.Proc Natl Acad Sci U S A2006https://conductscience.org/library/papers/16864780PubMed
616,902,930The 7 TM G-protein-coupled receptor target family.ChemMedChem2006https://conductscience.org/library/papers/16902930PubMed
717,373,883The use of bioluminescence resonance energy transfer for the study of therapeutic targets: application to tyrosine kinase receptors.Expert Opin Ther Targets2007https://conductscience.org/library/papers/17373883PubMed
811,897,050A comparison of ALPHAScreen, TR-FRET, and TRF as assay methods for FXR nuclear receptors.J Biomol Screen2002https://conductscience.org/library/papers/11897050PubMed
920,161,824Development of a HTRF kinase assay for determination of Syk activity.Curr Chem Genomics2008https://conductscience.org/library/papers/20161824PubMed
1010,838,425Introduction LANCEtrade mark vs. HTRF(R) Technologies (or Vice Versa).J Biomol Screen1999https://conductscience.org/library/papers/10838425PubMed

Cited by2

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 4 citations.

PMIDTitleJournalYearIn PapersSource
37,336,883Structural insights into regulation of the PEAK3 pseudokinase scaffold by 14-3-3.Nat Commun2023https://conductscience.org/library/papers/37336883PubMed
20,161,833HTRF: A technology tailored for drug discovery - a review of theoretical aspects and recent applications.Curr Chem Genomics2009https://conductscience.org/library/papers/20161833PubMed

Genes25

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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