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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 261 to 270 of 280

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Allelic, genotypic and phenotypic distributions of S-mephenytoin 4'-hydroxylase (CYP2C19) in healthy Caucasian populations of European descent throughout the world.
Xie HG, Stein CM, Kim RB, Wilkinson GR, Flockhart DA, Wood AJ
(1999) Pharmacogenetics 9: 539-49
MeSH Terms: Alleles, Aryl Hydrocarbon Hydroxylases, Cytochrome P-450 CYP2C19, Cytochrome P-450 Enzyme System, Europe, European Continental Ancestry Group, Gene Expression, Gene Frequency, Genotype, Humans, Mixed Function Oxygenases, Pharmacogenetics, Phenotype, Polymorphism, Genetic
Added December 10, 2013
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14 MeSH Terms
Genetic polymorphism of (S)-mephenytoin 4'-hydroxylation in populations of African descent.
Xie HG, Kim RB, Stein CM, Wilkinson GR, Wood AJ
(1999) Br J Clin Pharmacol 48: 402-8
MeSH Terms: Africa, African Continental Ancestry Group, Aryl Hydrocarbon Hydroxylases, Cytochrome P-450 CYP2C19, Cytochrome P-450 Enzyme System, Gene Frequency, Genotype, Humans, Hydroxylation, Mephenytoin, Mixed Function Oxygenases, Phenotype, Polymorphism, Genetic
Added December 10, 2013
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13 MeSH Terms
Low frequency of CYP2A6 gene polymorphism as revealed by a one-step polymerase chain reaction method.
Chen GF, Tang YM, Green B, Lin DX, Guengerich FP, Daly AK, Caporaso NE, Kadlubar FF
(1999) Pharmacogenetics 9: 327-32
MeSH Terms: Aryl Hydrocarbon Hydroxylases, Base Sequence, Cytochrome P-450 CYP2A6, Cytochrome P-450 Enzyme System, DNA Primers, Gene Frequency, Genotype, Humans, Introns, Mixed Function Oxygenases, Polymerase Chain Reaction, Polymorphism, Genetic
Added May 26, 2014
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12 MeSH Terms
Angiotensin type 2 receptor is important in the normal development of the ureter.
Hohenfellner K, Hunley TE, Schloemer C, Brenner W, Yerkes E, Zepp F, Brock JW, Kon V
(1999) Pediatr Nephrol 13: 187-91
MeSH Terms: Adolescent, Adult, Child, Child, Preschool, European Continental Ancestry Group, Gene Frequency, Genotype, Humans, Infant, Male, Receptor, Angiotensin, Type 1, Receptor, Angiotensin, Type 2, Receptors, Angiotensin, Ureter, Ureteral Obstruction, Urethra, Urethral Diseases
Added February 25, 2014
0 Communities
1 Members
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17 MeSH Terms
Relaxed replication of mtDNA: A model with implications for the expression of disease.
Chinnery PF, Samuels DC
(1999) Am J Hum Genet 64: 1158-65
MeSH Terms: Alleles, Computer Simulation, DNA Replication, DNA, Mitochondrial, Gene Dosage, Gene Frequency, Humans, Mitochondria, Mitochondrial Myopathies, Mitosis, Models, Genetic, Mutation, Phenotype, Time Factors
Added December 12, 2013
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14 MeSH Terms
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST
(1998) Hum Mol Genet 7: 1935-46
MeSH Terms: Adenine Nucleotides, Alleles, Animals, Fragile X Mental Retardation Protein, Fragile X Syndrome, Gene Frequency, Genetic Markers, Guanine Nucleotides, Haplotypes, Humans, Introns, Linkage Disequilibrium, Male, Microsatellite Repeats, Nerve Tissue Proteins, Pan troglodytes, Polymorphism, Genetic, Polymorphism, Single-Stranded Conformational, RNA-Binding Proteins, Trinucleotide Repeats
Added December 10, 2013
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20 MeSH Terms
Breast cancer and CYPIA1, GSTM1, and GSTT1 polymorphisms: evidence of a lack of association in Caucasians and African Americans.
Bailey LR, Roodi N, Verrier CS, Yee CJ, Dupont WD, Parl FF
(1998) Cancer Res 58: 65-70
MeSH Terms: African Continental Ancestry Group, Alleles, Breast Neoplasms, Cytochrome P-450 CYP1A1, European Continental Ancestry Group, Female, Gene Frequency, Genotype, Glutathione Transferase, Humans, Isoenzymes, Polymorphism, Genetic
Added March 21, 2014
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12 MeSH Terms
HLA and mate choice in humans.
Ober C, Weitkamp LR, Cox N, Dytch H, Kostyu D, Elias S
(1997) Am J Hum Genet 61: 497-504
MeSH Terms: Adult, Computer Simulation, Europe, Female, Founder Effect, Gene Frequency, HLA Antigens, Haplotypes, Histocompatibility Testing, Humans, Male, Marriage, North America
Added February 22, 2016
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13 MeSH Terms
Accurate inference of relationships in sib-pair linkage studies.
Boehnke M, Cox NJ
(1997) Am J Hum Genet 61: 423-9
MeSH Terms: Alleles, Diabetes Mellitus, Type 2, Family, Gene Frequency, Genetic Linkage, Genetic Markers, Humans, Likelihood Functions, Markov Chains, Models, Genetic, Reproducibility of Results
Added February 22, 2016
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11 MeSH Terms
Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.
Lee MP, DeBaun M, Randhawa G, Reichard BA, Elledge SJ, Feinberg AP
(1997) Am J Hum Genet 61: 304-9
MeSH Terms: Beckwith-Wiedemann Syndrome, Chromosomes, Human, Pair 11, CpG Islands, Cyclin-Dependent Kinase Inhibitor p57, Cyclin-Dependent Kinases, DNA Methylation, DNA Mutational Analysis, Dinucleoside Phosphates, Female, Frameshift Mutation, Gene Frequency, Genetic Heterogeneity, Genomic Imprinting, Humans, Infant, KCNQ Potassium Channels, KCNQ1 Potassium Channel, Male, Nuclear Proteins, Pedigree, Potassium Channels, Potassium Channels, Voltage-Gated
Added September 19, 2013
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22 MeSH Terms