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(Q)SAR Modeling and Safety Assessment in Regulatory Review

Clinical pharmacology and therapeutics, 2012-03, Vol.91 (3), p.529-534

2012

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An analysis of genetic toxicity, reproductive and developmental toxicity, and carcinogenicity data: I. Identification of carcinogens using surrogate endpoints

Regulatory toxicology and pharmacology, 2006-03, Vol.44 (2), p.83-96

2006

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An analysis of genetic toxicity, reproductive and developmental toxicity, and carcinogenicity data: II. Identification of genotoxicants, reprotoxicants, and carcinogens using in silico methods

Regulatory toxicology and pharmacology, 2006-03, Vol.44 (2), p.97-110

2006

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Predicting the carcinogenic potential of pharmaceuticals in rodents using molecular structural similarity and E-state indices

Regulatory toxicology and pharmacology, 2003-12, Vol.38 (3), p.243-259

2003

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Estimating the safe starting dose in phase I clinical trials and no observed effect level based on QSAR modeling of the human maximum recommended daily dose

Regulatory toxicology and pharmacology, 2004-12, Vol.40 (3), p.185-206

2004

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In silico screening of chemicals for bacterial mutagenicity using electrotopological E-state indices and MDL QSAR software

Regulatory toxicology and pharmacology, 2005-12, Vol.43 (3), p.313-323

2005

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Use of toxicological information in drug design

Journal of molecular graphics & modelling, 2000-12, Vol.18 (6), p.605

2000

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Understanding Genetic Toxicity Through Data Mining: The Process of Building Knowledge by Integrating Multiple Genetic Toxicity Databases

Toxicology mechanisms and methods, 2008-01, Vol.18 (2-3), p.277-295

2008

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Can the new genetic toxicology tests be used for regulatory safety decisions?

Environmental and molecular mutagenesis, 1999, Vol.33 (2), p.91-93

1999

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Does the prediction from a single (Q)SAR model based on a large comprehensive data set or the combined results from individual models each based on individual ICH S2 bacterial strains produce the better estimate of bacterial mutagenicity for ICH M7?

Toxicology letters, 2015-10, Vol.238 (2), p.S167-S167

2015

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Identification of structure-activity relationships for adverse effects of pharmaceuticals in humans: Part B. Use of (Q)SAR systems for early detection of drug-induced hepatobiliary and urinary tract toxicities

Regulatory toxicology and pharmacology, 2009-06, Vol.54 (1), p.23-42

2009

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Comparison of MC4PC and MDL-QSAR rodent carcinogenicity predictions and the enhancement of predictive performance by combining QSAR models

Regulatory toxicology and pharmacology, 2007-12, Vol.49 (3), p.172-182

2007

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Identification of structure–activity relationships for adverse effects of pharmaceuticals in humans. Part A: Use of FDA post-market reports to create a database of hepatobiliary and urinary tract toxicities

Regulatory toxicology and pharmacology, 2009-06, Vol.54 (1), p.1-22

2009

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Not all farming environments protect against the development of asthma and wheeze in children

Journal of allergy and clinical immunology, 2007-05, Vol.119 (5), p.1140-1147

2007

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Cytogenetic analysis of mouse metaphase II oocytes following exposure to tritiated water

Radiation research, 1987-09, Vol.111 (3), p.438

1987

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Priority-based assessment of food additives database of the U.S. Food and Drug Administration Center for Food Safety and Applied Nutrition

Environmental Health Perspectives [ENVIRON. HEALTH PERSPECT.]. 1991, 1991-12, Vol.96, p.85-89

1991

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Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling

Current drug discovery technologies, 2004-12, Vol.1 (4), p.243

2004

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Sister Chromatid Exchanges in Bone Marrow Cells of Mice Maintained on Tritiated Water

International journal of radiation biology, 1984-01, Vol.45 (3), p.251-256

1984

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Functional MR Imaging Techniques in Oncology in the Era of Personalized Medicine

Magnetic resonance imaging clinics of North America, 2016-02, Vol.24 (1), p.1-10

2016

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A system for simultaneous exposure of small animals to 60-Hz electric and magnetic fields

Bioelectromagnetics, 1991, Vol.12 (2), p.85

1991

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The distribution of moderately repeated DNA sequences among Chinese hamster chromosomes

Experimental cell research, 1978-03, Vol.112 (1), p.155-165

1978

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Preparation and identification of partially fractionated Chinese hamster chromosomes

Experimental cell research, 1978-03, Vol.112 (1), p.143-153

1978

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Sister chromatid exchanges induced in rabbit lymphocytes by ethylene oxide after inhalation exposure

Environmental mutagenesis, 1982, Vol.4 (2), p.121-134

1982

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PET Imaging of Prostate Cancer Using11 C-Acetate

PET clinics, 2009, Vol.4 (2), p.163-172

2009

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Landscape of current toxicity databases and database standards

Current opinion in drug discovery & development, 2006-01, Vol.9 (1), p.124

2006

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(Q)SAR Modeling and Safety Assessment in Regulatory Review

An analysis of genetic toxicity, reproductive and developmental toxicity, and carcinogenicity data: I. Identification of carcinogens using surrogate endpoints

An analysis of genetic toxicity, reproductive and developmental toxicity, and carcinogenicity data: II. Identification of genotoxicants, reprotoxicants, and carcinogens using in silico methods

Predicting the carcinogenic potential of pharmaceuticals in rodents using molecular structural similarity and E-state indices

Estimating the safe starting dose in phase I clinical trials and no observed effect level based on QSAR modeling of the human maximum recommended daily dose

In silico screening of chemicals for bacterial mutagenicity using electrotopological E-state indices and MDL QSAR software

Use of toxicological information in drug design

Understanding Genetic Toxicity Through Data Mining: The Process of Building Knowledge by Integrating Multiple Genetic Toxicity Databases

Can the new genetic toxicology tests be used for regulatory safety decisions?

Does the prediction from a single (Q)SAR model based on a large comprehensive data set or the combined results from individual models each based on individual ICH S2 bacterial strains produce the better estimate of bacterial mutagenicity for ICH M7?

Identification of structure-activity relationships for adverse effects of pharmaceuticals in humans: Part B. Use of (Q)SAR systems for early detection of drug-induced hepatobiliary and urinary tract toxicities

Comparison of MC4PC and MDL-QSAR rodent carcinogenicity predictions and the enhancement of predictive performance by combining QSAR models

Identification of structure–activity relationships for adverse effects of pharmaceuticals in humans. Part A: Use of FDA post-market reports to create a database of hepatobiliary and urinary tract toxicities

Not all farming environments protect against the development of asthma and wheeze in children

Cytogenetic analysis of mouse metaphase II oocytes following exposure to tritiated water

Priority-based assessment of food additives database of the U.S. Food and Drug Administration Center for Food Safety and Applied Nutrition

Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling

Sister Chromatid Exchanges in Bone Marrow Cells of Mice Maintained on Tritiated Water

Functional MR Imaging Techniques in Oncology in the Era of Personalized Medicine

A system for simultaneous exposure of small animals to 60-Hz electric and magnetic fields

The distribution of moderately repeated DNA sequences among Chinese hamster chromosomes

Preparation and identification of partially fractionated Chinese hamster chromosomes

Sister chromatid exchanges induced in rabbit lymphocytes by ethylene oxide after inhalation exposure

PET Imaging of Prostate Cancer Using11 C-Acetate

Landscape of current toxicity databases and database standards

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