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Some dogs kick when they dream

Nature (London), 2021-09

Blake, David G

2021

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Discovery of N-Phenyl-4-(thiazol-5-yl)pyrimidin-2-amine Aurora Kinase Inhibitors

Journal of medicinal chemistry, 2010-06, Vol.53 (11), p.4367-4378

2010

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Please consider my science-fiction story

Nature (London), 2017-12, Vol.552 (7683), p.142

Blake, David G

2017

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Please consider my science-fiction story

Nature (London), 2017-12, Vol.552 (7683), p.142-142

Blake, David G.

2017

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High throughput screens yield small molecule inhibitors of Leishmania CRK3:CYC6 cyclin-dependent kinase

PLoS neglected tropical diseases, 2011-04, Vol.5 (4), p.e1033-e1033

2011

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Low-city life

Nature physics, 2015-02, Vol.11 (2), p.200-200

Blake, David G.

2015

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A kite for Sarah

Nature (London), 2014-03, Vol.507 (7491), p.268-268

Blake, David G.

2014

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The Meisenheimer Complex as a Paradigm in Drug Discovery: Reversible Covalent Inhibition through C67 of the ATP Binding Site of PLK1

Cell chemical biology, 2018-09, Vol.25 (9), p.1107-1116.e4

2018

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To my father

Nature (London), 2013-01, Vol.493 (7434), p.714-714

Blake, David G.

2013

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Design, Synthesis, and Evaluation of 2-Methyl- and 2-Amino-N-aryl-4,5-dihydrothiazolo[4,5-h]quinazolin-8-amines as Ring-Constrained 2-Anilino-4-(thiazol-5-yl)pyrimidine Cyclin-Dependent Kinase Inhibitors

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.2136-2145

2010

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Langerhans cell histiocytosis associated with lichen sclerosus of the vulva: case report and review of the literature

Journal of cutaneous pathology, 2013-02, Vol.40 (2), p.279-283

2013

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A kite for Sarah: in search of freedom

Nature (London), 2014-03, Vol.507 (7491), p.268

Blake, David G

2014

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To my father: postcard from the edge

Nature (London), 2013-01, Vol.493 (7434), p.714

Blake, David G

2013

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A Quantitative Study of the in Vitro Binding of the C-Terminal Domain of p21 to PCNA: Affinity, Stoichiometry, and Thermodynamics

Biochemistry (Easton), 2000-06, Vol.39 (25), p.7388-7397

2000

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Regulation of human gamma-glutamylcysteine synthetase: co-ordinate induction of the catalytic and regulatory subunits in HepG2 cells

Biochemical journal, 1997-11, Vol.328 ( Pt 1) (1), p.99-104

1997

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Mutants of Tn3 resolvase which do not require accessory binding sites for recombination activity

The EMBO journal, 1999-03, Vol.18 (5), p.1407-1414

1999

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Abstract B182: Molecular basis for clinical development of the novel CDK2/9 inhibitor CYC065 in oncology

Molecular cancer therapeutics, 2015-12, Vol.14 (12_Supplement_2), p.B182-B182

2015

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Discovery and Characterization of 2-Anilino-4- (Thiazol-5-yl)Pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents

Chemistry & biology, 2010-10, Vol.17 (10), p.1111-1121

2010

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Abstract 5666: DNA repair defects enhance tumor cell sensitivity to sapacitabine

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.5666-5666

2012

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Abstract A33: Therapeutic potential of sapacitabine in ovarian cancers defective in homologous recombination

Clinical cancer research, 2013-10, Vol.19 (19_Supplement), p.A33-A33

2013

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Abstract 3886: Therapeutic potential of CDK inhibitors in MLL leukemias

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.3886-3886

2010

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Abstract 3502: Understanding the pathways involved in the repair of CNDAC induced DNA damage

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.3502-3502

2010

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Regulation of γ-glutamylcysteine synthetase regulatory subunit ( GLCLR) gene expression: identification of the major transcriptional start site in HT29 cells

Biochimica et biophysica acta, 1999-07, Vol.1446 (1), p.47-56

1999

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Abstract 4435: Discovery, biological characterization and oral antitumor activity of polo-like kinase 1 (Plk1) selective small molecule inhibitors

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.4435-4435

2010

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Overexpression of the regulatory subunit of γ-glutamylcysteine synthetase in HeLa cells increases γ-glutamylcysteine synthetase activity and confers drug resistance

Biochemical journal, 1999-02, Vol.337 (3), p.559-566

1999

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Some dogs kick when they dream

Discovery of N-Phenyl-4-(thiazol-5-yl)pyrimidin-2-amine Aurora Kinase Inhibitors

Please consider my science-fiction story

Please consider my science-fiction story

High throughput screens yield small molecule inhibitors of Leishmania CRK3:CYC6 cyclin-dependent kinase

Low-city life

A kite for Sarah

The Meisenheimer Complex as a Paradigm in Drug Discovery: Reversible Covalent Inhibition through C67 of the ATP Binding Site of PLK1

To my father

Design, Synthesis, and Evaluation of 2-Methyl- and 2-Amino-N-aryl-4,5-dihydrothiazolo[4,5-h]quinazolin-8-amines as Ring-Constrained 2-Anilino-4-(thiazol-5-yl)pyrimidine Cyclin-Dependent Kinase Inhibitors

Langerhans cell histiocytosis associated with lichen sclerosus of the vulva: case report and review of the literature

A kite for Sarah: in search of freedom

To my father: postcard from the edge

A Quantitative Study of the in Vitro Binding of the C-Terminal Domain of p21 to PCNA: Affinity, Stoichiometry, and Thermodynamics

Regulation of human gamma-glutamylcysteine synthetase: co-ordinate induction of the catalytic and regulatory subunits in HepG2 cells

Mutants of Tn3 resolvase which do not require accessory binding sites for recombination activity

Abstract B182: Molecular basis for clinical development of the novel CDK2/9 inhibitor CYC065 in oncology

Discovery and Characterization of 2-Anilino-4- (Thiazol-5-yl)Pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents

Abstract 5666: DNA repair defects enhance tumor cell sensitivity to sapacitabine

Abstract A33: Therapeutic potential of sapacitabine in ovarian cancers defective in homologous recombination

Abstract 3886: Therapeutic potential of CDK inhibitors in MLL leukemias

Abstract 3502: Understanding the pathways involved in the repair of CNDAC induced DNA damage

Regulation of γ-glutamylcysteine synthetase regulatory subunit ( GLCLR) gene expression: identification of the major transcriptional start site in HT29 cells

Abstract 4435: Discovery, biological characterization and oral antitumor activity of polo-like kinase 1 (Plk1) selective small molecule inhibitors

Overexpression of the regulatory subunit of γ-glutamylcysteine synthetase in HeLa cells increases γ-glutamylcysteine synthetase activity and confers drug resistance

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