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Defining the Target in Cancer of the Oesophagus: Direct Radiotherapy Planning with Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography

Clinical oncology (Royal College of Radiologists (Great Britain)), 2015-03, Vol.27 (3), p.160-167

2015

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Exploring the Patient's Experience of Receiving Clinical Care Which Incorporates the Use of Mobile Technology at the Bedside

Studies in health technology and informatics, 2021-12, Vol.284, p.469

2021

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Rhombomere origin plays a role in the specificity of cranial motor axon projections in the chick

The European journal of neuroscience, 1999-04, Vol.11 (4), p.1403-1413

1999

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Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells

Blood, 1999-11, Vol.94 (9), p.3193-3198

1999

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J. Moorman, A History of the Franciscan Order from its origins to the year 1517 (Book Review)

Revue d'Histoire Ecclésiastique, 1971, Vol.66 (2), p.605

Warrilow, J

1971

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COLVIN H. M. The White canons in England (Book Review)

Revue d'Histoire Ecclésiastique, 1952, Vol.47, p.225

Warrilow, J

1952

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Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells

Blood, 1999-11, Vol.94 (9), p.3193-3198

1999

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Women's perceptions of maternity carers

Midwifery, 1998-03, Vol.14 (1), p.48-53

1998

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The clinical candidate VT-1161 is a highly potent inhibitor of Candida albicans CYP51 but fails to bind the human enzyme

Antimicrobial agents and chemotherapy, 2014-12, Vol.58 (12), p.7121-7127

2014

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Cytochrome P450 168A1 from Pseudomonas aeruginosa is involved in the hydroxylation of biologically relevant fatty acids

PloS one, 2022-03, Vol.17 (3), p.e0265227

2022

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The Investigational Drug VT-1129 Is a Highly Potent Inhibitor of Cryptococcus Species CYP51 but Only Weakly Inhibits the Human Enzyme

Antimicrobial agents and chemotherapy, 2016-08, Vol.60 (8), p.4530-4538

2016

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Mechanism of Binding of Prothioconazole to Mycosphaerella graminicola CYP51 Differs from That of Other Azole Antifungals

Applied and Environmental Microbiology, 2011-02, Vol.77 (4), p.1460-1465

2011

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Azole Antifungal Agents To Treat the Human Pathogens Acanthamoeba castellanii and Acanthamoeba polyphaga through Inhibition of Sterol 14α-Demethylase (CYP51)

Antimicrobial agents and chemotherapy, 2015-08, Vol.59 (8), p.4707-4713

2015

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Prothioconazole and Prothioconazole-Desthio Activities against Candida albicans Sterol 14-α-Demethylase

Applied and Environmental Microbiology, 2013-03, Vol.79 (5), p.1639-1645

2013

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On the occurrence of cytochrome P450 in viruses

Proceedings of the National Academy of Sciences - PNAS, 2019-06, Vol.116 (25), p.12343-12352

2019

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The Tetrazole VT-1161 Is a Potent Inhibitor of Trichophyton rubrum through Its Inhibition of T. rubrum CYP51

Antimicrobial agents and chemotherapy, 2017-07, Vol.61 (7)

2017

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My Baby’s Movements: a stepped‐wedge cluster‐randomised controlled trial of a fetal movement awareness intervention to reduce stillbirths

BJOG : an international journal of obstetrics and gynaecology, 2022-01, Vol.129 (1), p.29-41

2022

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Complementation of a Saccharomyces cerevisiae ERG11/CYP51 (Sterol 14α-Demethylase) Doxycycline-Regulated Mutant and Screening of the Azole Sensitivity of Aspergillus fumigatus Isoenzymes CYP51A and CYP51B

Antimicrobial Agents and Chemotherapy, 2010-11, Vol.54 (11), p.4920-4923

2010

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Novel Substrate Specificity and Temperature-Sensitive Activity of Mycosphaerella graminicola CYP51 Supported by the Native NADPH Cytochrome P450 Reductase

Applied and Environmental Microbiology, 2015-05, Vol.81 (10), p.3379-3386

2015

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Discovery of a novel dual fungal CYP51/human 5-lipoxygenase inhibitor: implications for anti-fungal therapy

PloS one, 2013-06, Vol.8 (6), p.e65928

2013

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Expression of bacterial levanase in yeast enables simultaneous saccharification and fermentation of grass juice to bioethanol

Bioresource technology, 2011, Vol.102 (2), p.1503-1508

2011

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Isavuconazole and voriconazole inhibition of sterol 14α-demethylases (CYP51) from Aspergillus fumigatus and Homo sapiens

International journal of antimicrobial agents, 2019-10, Vol.54 (4), p.449-455

2019

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Expression, purification and use of the soluble domain of Lactobacillus paracasei β-fructosidase to optimise production of bioethanol from grass fructans

Bioresource technology, 2010-06, Vol.101 (12), p.4395-4402

2010

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Streptomyces coelicolor A3(2) CYP102 Protein, a Novel Fatty Acid Hydroxylase Encoded as a Heme Domain without an N-Terminal Redox Partner

Applied and Environmental Microbiology, 2010-03, Vol.76 (6), p.1975-1980

2010

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Clotrimazole as a potent agent for treating the oomycete fish pathogen Saprolegnia parasitica through inhibition of sterol 14α-demethylase (CYP51)

Applied and Environmental Microbiology, 2014-10, Vol.80 (19), p.6154-6166

2014

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Defining the Target in Cancer of the Oesophagus: Direct Radiotherapy Planning with Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography

Exploring the Patient's Experience of Receiving Clinical Care Which Incorporates the Use of Mobile Technology at the Bedside

Rhombomere origin plays a role in the specificity of cranial motor axon projections in the chick

Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells

J. Moorman, A History of the Franciscan Order from its origins to the year 1517 (Book Review)

COLVIN H. M. The White canons in England (Book Review)

Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells

Women's perceptions of maternity carers

The clinical candidate VT-1161 is a highly potent inhibitor of Candida albicans CYP51 but fails to bind the human enzyme

Cytochrome P450 168A1 from Pseudomonas aeruginosa is involved in the hydroxylation of biologically relevant fatty acids

The Investigational Drug VT-1129 Is a Highly Potent Inhibitor of Cryptococcus Species CYP51 but Only Weakly Inhibits the Human Enzyme

Mechanism of Binding of Prothioconazole to Mycosphaerella graminicola CYP51 Differs from That of Other Azole Antifungals

Azole Antifungal Agents To Treat the Human Pathogens Acanthamoeba castellanii and Acanthamoeba polyphaga through Inhibition of Sterol 14α-Demethylase (CYP51)

Prothioconazole and Prothioconazole-Desthio Activities against Candida albicans Sterol 14-α-Demethylase

On the occurrence of cytochrome P450 in viruses

The Tetrazole VT-1161 Is a Potent Inhibitor of Trichophyton rubrum through Its Inhibition of T. rubrum CYP51

My Baby’s Movements: a stepped‐wedge cluster‐randomised controlled trial of a fetal movement awareness intervention to reduce stillbirths

Complementation of a Saccharomyces cerevisiae ERG11/CYP51 (Sterol 14α-Demethylase) Doxycycline-Regulated Mutant and Screening of the Azole Sensitivity of Aspergillus fumigatus Isoenzymes CYP51A and CYP51B

Novel Substrate Specificity and Temperature-Sensitive Activity of Mycosphaerella graminicola CYP51 Supported by the Native NADPH Cytochrome P450 Reductase

Discovery of a novel dual fungal CYP51/human 5-lipoxygenase inhibitor: implications for anti-fungal therapy

Expression of bacterial levanase in yeast enables simultaneous saccharification and fermentation of grass juice to bioethanol

Isavuconazole and voriconazole inhibition of sterol 14α-demethylases (CYP51) from Aspergillus fumigatus and Homo sapiens

Expression, purification and use of the soluble domain of Lactobacillus paracasei β-fructosidase to optimise production of bioethanol from grass fructans

Streptomyces coelicolor A3(2) CYP102 Protein, a Novel Fatty Acid Hydroxylase Encoded as a Heme Domain without an N-Terminal Redox Partner

Clotrimazole as a potent agent for treating the oomycete fish pathogen Saprolegnia parasitica through inhibition of sterol 14α-demethylase (CYP51)

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