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Interplays of AMPK and TOR in Autophagy Regulation in Yeast

Cells (Basel, Switzerland), 2023-02, Vol.12 (4), p.519

2023

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Crosstalk between the mTOR and DNA Damage Response Pathways in Fission Yeast

Cells (Basel, Switzerland), 2021-02, Vol.10 (2), p.305

2021

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Flemingins G–O, Cytotoxic and Antioxidant Constituents of the Leaves of Flemingia grahamiana

Journal of natural products (Washington, D.C.), 2014-09, Vol.77 (9), p.2060-2067

2014

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Cytotoxic quinones from the roots of Aloe dawei

Molecules (Basel, Switzerland), 2014-03, Vol.19 (3), p.3264-3273

2014

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Anthraquinones of the roots of Pentas micrantha

Molecules (Basel, Switzerland), 2013-01, Vol.18 (1), p.311-321

2013

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Histone Deacetylase Inhibitor Trichostatin A Represses Estrogen Receptor α-Dependent Transcription and Promotes Proteasomal Degradation of Cyclin D1 in Human Breast Carcinoma Cell Lines

Clinical cancer research, 2004-12, Vol.10 (23), p.8094-8104

2004

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The regulation of cyclin D1 degradation: roles in cancer development and the potential for therapeutic invention

Molecular cancer, 2007-04, Vol.6 (1), p.24-24

Alao, John P

2007

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Caffeine as a tool for investigating the integration of Cdc25 phosphorylation, activity and ubiquitin-dependent degradation in Schizosaccharomyces pombe

Cell division, 2020-06, Vol.15 (1), p.1-10, Article 10

2020

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Selective inhibition of RET mediated cell proliferation in vitro by the kinase inhibitor SPP86

BMC cancer, 2014-11, Vol.14 (1), p.853-853, Article 853

2014

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Suppression of sensitivity to drugs and antibiotics by high external cation concentrations in fission yeast

PloS one, 2015-03, Vol.10 (3), p.e0119297

2015

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Caffeine Stabilises Fission Yeast Wee1 in a Rad24-Dependent Manner but Attenuates Its Expression in Response to DNA Damage

Microorganisms (Basel), 2020-09, Vol.8 (10), p.1512

2020

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The ATM and ATR inhibitors CGK733 and caffeine suppress cyclin D1 levels and inhibit cell proliferation

Radiation oncology (London, England), 2009-11, Vol.4 (1), p.51-51, Article 51

2009

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Caffeine stabilizes Cdc25 independently of Rad3 in Schizosaccharomyces pombe contributing to checkpoint override

Molecular microbiology, 2014-05, Vol.92 (4), p.777-796

2014

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Azastilbenes: a cut-off to p38 MAPK inhibitorsElectronic supplementary information (ESI) available: General experimental procedure, characterization of synthesized compounds, 1H NMR and 13C NMR spectra. See DOI: 10.1039/c3ob27449g

2013-06

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Design, Synthesis, and Biological Evaluation of Chromone-Based p38 MAP Kinase Inhibitors

Journal of medicinal chemistry, 2011-10, Vol.54 (20), p.7427-7431

2011

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Azastilbenes: a cut-off to p38 MAPK inhibitors

Organic & biomolecular chemistry, 2013-07, Vol.11 (27), p.4526-4536

2013

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A role for Myh1 in DNA repair after treatment with strand-breaking and crosslinking chemotherapeutic agents

Environmental and molecular mutagenesis, 2013-06, Vol.54 (5), p.327-337

2013

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Inhibition of type I histone deacetylase increases resistance of checkpoint-deficient cells to genotoxic agents through mitotic delay

Molecular cancer therapeutics, 2009-09, Vol.8 (9), p.2606-2615

2009

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Busseihydroquinones A–D from the Roots of Pentas bussei

Journal of natural products (Washington, D.C.), 2012-07, Vol.75 (7), p.1299-1304

2012

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Preparation of 3-Substituted-1-Isopropyl-1H-pyrazolo 3,4-d pyrimidin-4-amines as RET Kinase Inhibitors

Journal of medicinal chemistry, 2012, Vol.55 4872-4876 (10), p.4872

2012

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Preparation of 3-Substituted-1-Isopropyl-1H-pyrazolo 3,4-d pyrimidin-4-amines as RET Kinase Inhibitors

Journal of medicinal chemistry, 2012, Vol.55 (10), p.4872

2012

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Role of glycogen synthase kinase 3 beta (GSK3beta) in mediating the cytotoxic effects of the histone deacetylase inhibitor trichostatin A (TSA) in MCF-7 breast cancer cells

Molecular cancer, 2006-10, Vol.5 (1), p.40-40

2006

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Antiplasmodial quinones from Pentas longiflora and Pentas lanceolata

Planta medica, 2012-01, Vol.78 (1), p.31-35

2012

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The ATM regulated DNA damage response pathway as a chemo- and radiosensitisation target

Expert opinion on drug discovery, 2009-05, Vol.4 (5), p.495-505

Alao, John P

2009

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Hyperosmosis enhances radiation and hydroxyurea resistance of S. pombe checkpoint mutants through the spindle checkpoint and delayed cytokinesis

Molecular microbiology, 2010, Vol.77 (1), p.143

2010

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Interplays of AMPK and TOR in Autophagy Regulation in Yeast

Crosstalk between the mTOR and DNA Damage Response Pathways in Fission Yeast

Flemingins G–O, Cytotoxic and Antioxidant Constituents of the Leaves of Flemingia grahamiana

Cytotoxic quinones from the roots of Aloe dawei

Anthraquinones of the roots of Pentas micrantha

Histone Deacetylase Inhibitor Trichostatin A Represses Estrogen Receptor α-Dependent Transcription and Promotes Proteasomal Degradation of Cyclin D1 in Human Breast Carcinoma Cell Lines

The regulation of cyclin D1 degradation: roles in cancer development and the potential for therapeutic invention

Caffeine as a tool for investigating the integration of Cdc25 phosphorylation, activity and ubiquitin-dependent degradation in Schizosaccharomyces pombe

Selective inhibition of RET mediated cell proliferation in vitro by the kinase inhibitor SPP86

Suppression of sensitivity to drugs and antibiotics by high external cation concentrations in fission yeast

Caffeine Stabilises Fission Yeast Wee1 in a Rad24-Dependent Manner but Attenuates Its Expression in Response to DNA Damage

The ATM and ATR inhibitors CGK733 and caffeine suppress cyclin D1 levels and inhibit cell proliferation

Caffeine stabilizes Cdc25 independently of Rad3 in Schizosaccharomyces pombe contributing to checkpoint override

Azastilbenes: a cut-off to p38 MAPK inhibitorsElectronic supplementary information (ESI) available: General experimental procedure, characterization of synthesized compounds, 1H NMR and 13C NMR spectra. See DOI: 10.1039/c3ob27449g

Design, Synthesis, and Biological Evaluation of Chromone-Based p38 MAP Kinase Inhibitors

Azastilbenes: a cut-off to p38 MAPK inhibitors

A role for Myh1 in DNA repair after treatment with strand-breaking and crosslinking chemotherapeutic agents

Inhibition of type I histone deacetylase increases resistance of checkpoint-deficient cells to genotoxic agents through mitotic delay

Busseihydroquinones A–D from the Roots of Pentas bussei

Preparation of 3-Substituted-1-Isopropyl-1H-pyrazolo 3,4-d pyrimidin-4-amines as RET Kinase Inhibitors

Preparation of 3-Substituted-1-Isopropyl-1H-pyrazolo 3,4-d pyrimidin-4-amines as RET Kinase Inhibitors

Role of glycogen synthase kinase 3 beta (GSK3beta) in mediating the cytotoxic effects of the histone deacetylase inhibitor trichostatin A (TSA) in MCF-7 breast cancer cells

Antiplasmodial quinones from Pentas longiflora and Pentas lanceolata

The ATM regulated DNA damage response pathway as a chemo- and radiosensitisation target

Hyperosmosis enhances radiation and hydroxyurea resistance of S. pombe checkpoint mutants through the spindle checkpoint and delayed cytokinesis

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