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Publications by Pervez F. Firozi
Polymorphisms of Phase II Xenobiotic-Metabolizing and DNA Repair Genes and in Vitro N-Ethyl-N-Nitrosourea-Induced O6-Ethylguanine Levels in Human Lymphocytes
Mutation Research - Genetic Toxicology and Environmental Mutagenesis
Mutagenesis
Toxicology
Health
Genetics
Related publications
Specificities of Human, Rat andE.coliO6-methylguanine-DNA Methyltransferases Towards the Repair of O6-Methyl and O6-Ethylguanine in DNA
Nucleic Acids Research
Genetics
Enhancement by O6-Benzyl-N2-Acetylguanosine of N'-[2-Chloroethyl]-N-[2-(Methylsulphonyl)ethyl]-N'-Nitrosourea Therapeutic Index on Nude Mice Bearing Resistant Human Melanoma
British Journal of Cancer
Cancer Research
Oncology
N-Methyl-N-Nitrosourea-Induced Retinal Degeneration in Animals
Acta Histochemica et Cytochemica
Cell Biology
Biochemistry
Histology
Forensic Medicine
Pathology
Physiology
Osteopontin Expression in Intratumoral Astrocytes Marks Tumor Progression in Gliomas Induced by Prenatal Exposure to N-Ethyl-N-Nitrosourea
American Journal of Pathology
Forensic Medicine
Pathology
Relationship Between O6-Alkylguanine-Dna Alkyltransferase Activity and N-Methyl-N'-Nitro-N-Nitrosoguanidine-Induced Mutation, Transformation, and Cytotoxicity in C3h/10t1/2 Cells Expressing Exogenous Alkyltransferase Genes.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Skeletal Muscles Express the Xenobiotic-Metabolizing Enzyme Arylamine N-Acetyltransferase
Journal of Histochemistry and Cytochemistry
Anatomy
Histology
Donepezil Delays Photoreceptor Apoptosis Induced by N-Methyl-N-Nitrosourea in Mice
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Increased Sensitivity of Lymphocytes From Patients With Systemic Autoimmune Diseases to DNA Alkylation by the Methylating Carcinogen N-Methyl-N-Nitrosourea.
Annals of the Rheumatic Diseases
Immunology
Molecular Biology
Biochemistry
Rheumatology
Allergy
Genetics
A Mouse With an N-Ethyl-N-Nitrosourea (ENU) Induced Trp589Arg Galnt3 Mutation Represents a Model for Hyperphosphataemic Familial Tumoural Calcinosis
PLoS ONE
Multidisciplinary
