(Q27665991)

1

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Payal R Sheth

2

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Andrea D Basso

3

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Sunil Paliwal

4

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Kimberly Gray

5

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Thierry O Fischmann

6

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Hung V Le

Targeting cancer with small molecule kinase inhibitors

7

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language of work or name

English

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publication date

3 January 2011

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published in

FEBS Letters

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volume

585

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issue

1

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page(s)

104-10

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cites work

1 reference

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A comprehensive catalogue of somatic mutations from a human cancer genome

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Protein kinase CK2: structure, regulation and role in cellular decisions of life and death

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Casein kinase II alpha transgene-induced murine lymphoma: relation to theileriosis in cattle.

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Protein kinase CK2 in mammary gland tumorigenesis

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Antisense oligonucleotides against protein kinase CK2-alpha inhibit growth of squamous cell carcinoma of the head and neck in vitro

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Induction of cell death in antiestrogen resistant human breast cancer cells by the protein kinase CK2 inhibitor DMAT.

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Optimization of protein kinase CK2 inhibitors derived from 4,5,6,7-tetrabromobenzimidazole

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Inhibition of protein kinase CK2 by condensed polyphenolic derivatives. An in vitro and in vivo study

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Discovery of a potent and selective protein kinase CK2 inhibitor by high-throughput docking

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New potent dual inhibitors of CK2 and Pim kinases: discovery and structural insights

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New protein kinase CK2 inhibitors: jumping out of the catalytic box.

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The CK2 alpha/CK2 beta interface of human protein kinase CK2 harbors a binding pocket for small molecules

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Protein kinase CK2 in health and disease: Protein kinase CK2: from structures to insights.

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Thermodynamic stability of carbonic anhydrase: measurements of binding affinity and stoichiometry using ThermoFluor.

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Processing of X-ray diffraction data collected in oscillation mode

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Automatic processing of rotation diffraction data from crystals of initially unknown symmetry and cell constants

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The CCP4 suite: programs for protein crystallography

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MOLREP: an Automated Program for Molecular Replacement

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Features and development of Coot

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The catalytic subunit of human protein kinase CK2 structurally deviates from its maize homologue in complex with the nucleotide competitive inhibitor emodin

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DaliLite workbench for protein structure comparison

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