(Q40770313)

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Comparison of the biochemical and kinetic properties of the type 1 receptor tyrosine kinase intracellular domains. Demonstration of differential sensitivity to kinase inhibitors

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scholarly article

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Europe PubMed Central

23 September 2017

Comparison of the biochemical and kinetic properties of the type 1 receptor tyrosine kinase intracellular domains. Demonstration of differential sensitivity to kinase inhibitors (English)

1 reference

Europe PubMed Central

23 September 2017

author name string

Perry S Brignola

1

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Europe PubMed Central

23 September 2017

Karen Lackey

2

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Europe PubMed Central

23 September 2017

Sue H Kadwell

3

1 reference

Europe PubMed Central

23 September 2017

Christine Hoffman

4

1 reference

Europe PubMed Central

23 September 2017

Earnest Horne

5

1 reference

Europe PubMed Central

23 September 2017

H Luke Carter

6

1 reference

Europe PubMed Central

23 September 2017

J Darren Stuart

7

1 reference

Europe PubMed Central

23 September 2017

Kevin Blackburn

8

1 reference

Europe PubMed Central

23 September 2017

Mary B Moyer

9

1 reference

Europe PubMed Central

23 September 2017

Krystal J Alligood

10

1 reference

Europe PubMed Central

23 September 2017

Wilson B Knight

11

1 reference

Europe PubMed Central

23 September 2017

Edgar R Wood

12

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23 September 2017

language of work or name

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publication date

5 November 2001

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23 September 2017

Journal of Biological Chemistry

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23 September 2017

277

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23 September 2017

2

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23 September 2017

1576-1585

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Europe PubMed Central

23 September 2017

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1 reference

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Phase II study of receptor-enhanced chemosensitivity using recombinant humanized anti-p185HER2/neu monoclonal antibody plus cisplatin in patients with HER2/neu-overexpressing metastatic breast cancer refractory to chemotherapy treatment

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Homogeneous proximity tyrosine kinase assays: scintillation proximity assay versus homogeneous time-resolved fluorescence.

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A scintillation proximity assay for the Raf/MEK/ERK kinase cascade: high-throughput screening and identification of selective enzyme inhibitors

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Aggregation-induced activation of the epidermal growth factor receptor protein tyrosine kinase

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Physicochemical characterization of the cytoplasmic domain of the epidermal growth factor receptor and evidence for conformational changes associated with its activation by ammonium sulphate

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Magnetic resonance and kinetic studies of the manganese(II) ion and substrate complexes of the catalytic subunit of adenosine 3',5'-monophosphate dependent protein kinase from bovine heart

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Requirement for an additional divalent metal cation to activate protein tyrosine kinases.

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Tyrosine kinase inhibitors. 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth factor receptor

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Activation of the EGF receptor tyrosine kinase by divalent metal ions: comparison of holoreceptor and isolated kinase domain properties

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21 January 2018

Ligand and p185c-neu density govern receptor interactions and tyrosine kinase activation

1 reference

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21 January 2018

Crystal structure of the catalytic subunit of cAMP-dependent protein kinase complexed with MgATP and peptide inhibitor

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Substrate specificity of the oncoprotein v-Fps: site-specific mutagenesis of the putative P+1 pocket

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Thiol and amino analogues as alternate substrates for glycerokinase from Candida mycoderma

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Structure-activity relationships for 4-anilinoquinazolines as potent inhibitors at the ATP binding site of the epidermal growth factor receptor in vitro

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21 January 2018

Inhibition of epidermal-growth-factor-receptor-dependent signalling by tyrphostins A25 and AG1478 blocks growth and induces apoptosis in colorectal tumor cells in vitro

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21 January 2018

Adenosine cyclic 3',5'-monophosphate dependent protein kinase: kinetic mechanism for the bovine skeletal muscle catalytic subunit

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21 January 2018

Engineering the substrate specificity of the Abl tyrosine kinase

1 reference

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21 January 2018

Identifiers

10.1074/JBC.M105907200

1 reference

Europe PubMed Central

23 September 2017

1 reference

Europe PubMed Central

23 September 2017

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