Functional effects of single nucleotide polymorphisms in the coding region of human N-acetyltransferase 1
暂无分享,去创建一个
[1] Lippincott-Schwartz,et al. Supporting Online Material Materials and Methods Som Text Figs. S1 to S8 Table S1 Movies S1 to S3 a " Silent " Polymorphism in the Mdr1 Gene Changes Substrate Specificity Corrected 30 November 2007; See Last Page , 2022 .
[2] M. Doll,et al. Functional characterization of the A411T (L137F) and G364A (D122N) genetic polymorphisms in human N-acetyltransferase 2 , 2007, Pharmacogenetics and genomics.
[3] G. Shaw,et al. Risk of limb deficiency defects associated with NAT1, NAT2, GSTT1, GSTM1, and NOS3 genetic variants, maternal smoking, and vitamin supplement intake , 2006, American journal of medical genetics. Part A.
[4] X. Jianming,et al. N-Acetyltransferase-1 gene polymorphisms and correlation between genotype and its activity in a central Chinese Han population. , 2006, Clinica chimica acta; international journal of clinical chemistry.
[5] M. Doll,et al. Functional properties of an alternative, tissue-specific promoter for human arylamine N-acetyltransferase 1 , 2006, Pharmacogenetics and genomics.
[6] L. E. Mitchell,et al. Loss of function polymorphisms in NAT1 protect against spina bifida , 2006, Human Genetics.
[7] D. Hein,et al. N-acetyltransferase 2 genetic polymorphism: effects of carcinogen and haplotype on urinary bladder cancer risk , 2006, Oncogene.
[8] Andrew D. Johnson,et al. Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C>T affects mRNA stability , 2005, Pharmacogenetics and genomics.
[9] L. E. Mitchell,et al. The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida. , 2005, Birth defects research. Clinical and molecular teratology.
[10] G. Fakis,et al. Arylamine N-Acetyltransferases: What We Learn from Genes and Genomes , 2005, Drug metabolism reviews.
[11] G. Shaw,et al. Periconceptional multivitamin intake during early pregnancy, genetic variation of acetyl-N-transferase 1 (NAT1), and risk for orofacial clefts. , 2004, Birth defects research. Part A, Clinical and molecular teratology.
[12] J. States,et al. The T341C (Ile114Thr) polymorphism of N-acetyltransferase 2 yields slow acetylator phenotype by enhanced protein degradation. , 2004, Pharmacogenetics.
[13] J. States,et al. Identification of the major promoter and non-coding exons of the human arylamine N-acetyltransferase 1 gene (NAT1). , 2004, Pharmacogenetics.
[14] R. Minchin,et al. Proteasomal Degradation of N-Acetyltransferase 1 Is Prevented by Acetylation of the Active Site Cysteine , 2004, Journal of Biological Chemistry.
[15] G. Shaw,et al. Maternal Smoking and the Risk of Orofacial Clefts: Susceptibility With NAT1 and NAT2 Polymorphisms , 2004, Epidemiology.
[16] D. Hein. Molecular genetics and function of NAT1 and NAT2: role in aromatic amine metabolism and carcinogenesis. , 2002, Mutation research.
[17] M. Doll,et al. Rapid genotype method to distinguish frequent and/or functional polymorphisms in human N-acetyltransferase-1. , 2002, Analytical biochemistry.
[18] M. Doll,et al. Functional Genomics of C190T Single Nucleotide Polymorphism in Human N-Acetyltransferase 2 , 2002, Biological chemistry.
[19] R. Minchin,et al. Pharmacogenetics of the arylamine N-acetyltransferases , 2002, The Pharmacogenomics Journal.
[20] M. Doll,et al. Functional characterization of nucleotide polymorphisms in the coding region of N-acetyltransferase 1. , 2001, Pharmacogenetics.
[21] W. Weber,et al. Characterization of naturally occurring and recombinant human N-acetyltransferase variants encoded by NAT1. , 2000, Molecular pharmacology.
[22] D. Grant,et al. Update on consensus arylamine N-acetyltransferase gene nomenclature. , 2000, Pharmacogenetics.
[23] H. Dhaini,et al. Arylamine N-acetyltransferase 1 (NAT1) genotypes in a Lebanese population. , 2000, Pharmacogenetics.
[24] M. Doll,et al. Molecular genetics and epidemiology of the NAT1 and NAT2 acetylation polymorphisms. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[25] M. Doll,et al. Molecular Genetics and Epidemiology of the NAT 1 and NAT 2 Acetylation Polymorphisms 1 , 2000 .
[26] J. Brockmöller,et al. Correlation between genotype and phenotype of the human arylamine N-acetyltransferase type 1 (NAT1). , 1999, Biochemical pharmacology.
[27] J. Basilion,et al. Single-nucleotide polymorphisms can cause different structural folds of mRNA. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[28] T. Rustan,et al. Prostate-specific human N-acetyltransferase 2 (NAT2) expression in the mouse. , 1999, The Journal of pharmacology and experimental therapeutics.
[29] N. Probst-Hensch,et al. Variants of N-acetyltransferase NAT1 and a case-control study of colorectal adenomas. , 1998, Pharmacogenetics.
[30] D. Grant,et al. Identification and characterization of variant alleles of human acetyltransferase NAT1 with defective function using p-aminosalicylate as an in-vivo and in-vitro probe. , 1998, Pharmacogenetics.
[31] R. Minchin,et al. Functional polymorphism of the human arylamine N-acetyltransferase type 1 gene caused by C190T and G560A mutations. , 1998, Pharmacogenetics.
[32] D. Grant,et al. Human acetyltransferase polymorphisms. , 1997, Mutation research.
[33] T. Rustan,et al. Identification of a novel allele at the human NAT1 acetyltransferase locus. , 1997, Biochemical and biophysical research communications.
[34] D. Grant,et al. Study of the role of the highly conserved residues Arg9 and Arg64 in the catalytic function of human N-acetyltransferases NAT1 and NAT2 by site-directed mutagenesis. , 1997, The Biochemical journal.