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Engrailed-2 (EN2): A Tumor Specific Urinary Biomarker for the Early Diagnosis of Prostate Cancer

Clinical cancer research, 2011-03, Vol.17 (5), p.1090-1098

2011

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Synergistic effects of oncolytic reovirus and docetaxel chemotherapy in prostate cancer

BMC cancer, 2011-06, Vol.11 (1), p.221-221, Article 221

2011

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Processing and intracellular location of human astrovirus non-structural proteins

Journal of general virology, 1999-10, Vol.80 ( Pt 10) (10), p.2607-2611

1999

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Abstract A17: Antagonizing HOX function triggers apoptosis in prostate cancer cells

Cancer research (Chicago, Ill.), 2012-02, Vol.72 (4_Supplement), p.A17-A17

2012

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Abstract 2723: The chorio-allantoicmembrane (CAM) model for testing HOX gene antagonism in pancreatic cancer

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.2723-2723

2013

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Caspases are not involved in the cleavage of translation initiation factor eIF4GI during picornavirus infection

Journal of general virology, 2000-07, Vol.81 (7), p.1703-1707

2000

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Abstract 3100: HOX transcription factors promote cell survival in breast cancer

Cancer research (Chicago, Ill.), 2011-04, Vol.71 (8_Supplement), p.3100-3100

2011

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Processing and intracellular location of human astrovirusnon-structural proteins

Journal of general virology, 1999-10, Vol.80 (10), p.2607-2611

1999

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Poliovirus Induces an Early Impairment of Mitochondrial Function by Inhibiting Succinate Dehydrogenase Activity: Volume 271, Number 3 (2000), pages 610–614 (doi:10.1006/bbrc.2000.2675)

Biochemical and biophysical research communications, 2000-06, Vol.272 (3), p.966-966

2000

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Poliovirus Induces an Early Impairment of Mitochondrial Function by Inhibiting Succinate Dehydrogenase Activity

Biochemical and biophysical research communications, 2000-05, Vol.271 (3), p.610-614

2000

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Poliovirus Induces an Early Impairment of Mitochondrial Function by Inhibiting Succinate Dehydrogenase Activity

Biochemical and biophysical research communications, 2000-06, Vol.272 (3), p.966

2000

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Operator 4.0 or Maker 1.0? Exploring the implications of Industrie 4.0 for innovation, safety and quality of work in small economies and enterprises

Computers & industrial engineering, 2020-01, Vol.139, p.105486, Article 105486

2020

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The transformation to data analytics in Big-Four financial audit: what, why and how?

Pacific accounting review, 2022-08, Vol.34 (4), p.569-584

2022

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A uniform measurement expression for cross method comparison of nanoparticle aggregate size distributions

Analyst (London), 2015-08, Vol.140 (15), p.5257-5267

2015

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Structure-Based Design of Orally Bioavailable 1H‑Pyrrolo[3,2‑c]pyridine Inhibitors of Mitotic Kinase Monopolar Spindle 1 (MPS1)

Journal of medicinal chemistry, 2013-12, Vol.56 (24), p.10045-10065

2013

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Effects of oral anticoagulation for atrial fibrillation after spontaneous intracranial haemorrhage in the UK: a randomised, open-label, assessor-masked, pilot-phase, non-inferiority trial

Lancet neurology, 2021-10, Vol.20 (10), p.842-853

2021

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CCT244747 Is a Novel Potent and Selective CHK1 Inhibitor with Oral Efficacy Alone and in Combination with Genotoxic Anticancer Drugs

Clinical cancer research, 2012-10, Vol.18 (20), p.5650-5661

2012

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Development of a sample preparation approach to measure the size of nanoparticle aggregates by electron microscopy

Particuology, 2019-08, Vol.45, p.49-57

2019

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Inhibition of the heat shock protein 90 molecular chaperone in vitro and in vivo by novel, synthetic, potent resorcinylic pyrazole/isoxazole amide analogues

Molecular cancer therapeutics, 2007-04, Vol.6 (4), p.1198-1211

2007

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Trans-activation of the DNA-damage signalling protein kinase Chk2 by T-loop exchange

The EMBO journal, 2006-07, Vol.25 (13), p.3179-3190

2006

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The preclinical pharmacology and therapeutic activity of the novel CHK1 inhibitor SAR-020106

Molecular cancer therapeutics, 2010-01, Vol.9 (1), p.89-100

2010

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Structure-Guided Evolution of Potent and Selective CHK1 Inhibitors through Scaffold Morphing

Journal of medicinal chemistry, 2011-12, Vol.54 (24), p.8328-8342

2011

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Structure-Based Design of Orally Bioavailable 1 H -Pyrrolo[3,2- c ]pyridine Inhibitors of Mitotic Kinase Monopolar Spindle 1 (MPS1)

Journal of medicinal chemistry, 2013-12, Vol.56 (24), p.10045-10065

2013

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Engrailed-2 (EN2): A Tumor Specific Urinary Biomarker for the Early Diagnosis of Prostate Cancer

Synergistic effects of oncolytic reovirus and docetaxel chemotherapy in prostate cancer

Processing and intracellular location of human astrovirus non-structural proteins

Abstract A17: Antagonizing HOX function triggers apoptosis in prostate cancer cells

Abstract 2723: The chorio-allantoicmembrane (CAM) model for testing HOX gene antagonism in pancreatic cancer

Caspases are not involved in the cleavage of translation initiation factor eIF4GI during picornavirus infection

Abstract 3100: HOX transcription factors promote cell survival in breast cancer

Processing and intracellular location of human astrovirusnon-structural proteins

Poliovirus Induces an Early Impairment of Mitochondrial Function by Inhibiting Succinate Dehydrogenase Activity: Volume 271, Number 3 (2000), pages 610–614 (doi:10.1006/bbrc.2000.2675)

Poliovirus Induces an Early Impairment of Mitochondrial Function by Inhibiting Succinate Dehydrogenase Activity

Poliovirus Induces an Early Impairment of Mitochondrial Function by Inhibiting Succinate Dehydrogenase Activity

NVP-AUY922: a novel heat shock protein 90 inhibitor active against xenograft tumor growth, angiogenesis, and metastasis

Operator 4.0 or Maker 1.0? Exploring the implications of Industrie 4.0 for innovation, safety and quality of work in small economies and enterprises

The transformation to data analytics in Big-Four financial audit: what, why and how?

A uniform measurement expression for cross method comparison of nanoparticle aggregate size distributions

Structure-Based Design of Orally Bioavailable 1H‑Pyrrolo[3,2‑c]pyridine Inhibitors of Mitotic Kinase Monopolar Spindle 1 (MPS1)

Effects of oral anticoagulation for atrial fibrillation after spontaneous intracranial haemorrhage in the UK: a randomised, open-label, assessor-masked, pilot-phase, non-inferiority trial

CCT244747 Is a Novel Potent and Selective CHK1 Inhibitor with Oral Efficacy Alone and in Combination with Genotoxic Anticancer Drugs

Development of a sample preparation approach to measure the size of nanoparticle aggregates by electron microscopy

Inhibition of the heat shock protein 90 molecular chaperone in vitro and in vivo by novel, synthetic, potent resorcinylic pyrazole/isoxazole amide analogues

Multiparameter Lead Optimization to Give an Oral Checkpoint Kinase 1 (CHK1) Inhibitor Clinical Candidate: (R)‑5-((4-((Morpholin-2-ylmethyl)amino)-5-(trifluoromethyl)pyridin-2-yl)amino)pyrazine-2-carbonitrile (CCT245737)

Trans-activation of the DNA-damage signalling protein kinase Chk2 by T-loop exchange

The preclinical pharmacology and therapeutic activity of the novel CHK1 inhibitor SAR-020106

Structure-Guided Evolution of Potent and Selective CHK1 Inhibitors through Scaffold Morphing

Structure-Based Design of Orally Bioavailable 1 H -Pyrrolo[3,2- c ]pyridine Inhibitors of Mitotic Kinase Monopolar Spindle 1 (MPS1)

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