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Important Insight On SNP

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SNP
Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases
Usefulness of Single Nucleotide Polymorphism Data for Estimating Population Parameters
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
Single nucleotide polymorphisms as tools in human genetics
Single-nucleotide polymorphisms can cause different structural folds of mRNA
Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory
Slow axonal transport: stop and go traffic in the axon
Novel Polymorphisms in the Promoter and 5'UTR Regions of the human vascular endothelial growth factor gene
SNP discovery and linkage mapping of bovine cytokine genes
Single nucleotide polymorphism spectra in newborns and centenarians: identification of genes coding for rise of mortal disease
Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography
A novel assay for allelic discrimination that combines the fluorogenic 5'nuclease polymerase chain reaction (TaqMan) and mismatch amplification mutation assay
A cluster of single nucleotide polymorphisms in the 5'-leader of the human dopamine D3 receptor gene (DRD3) and its relationship to schizophrenia
An SNP map of human chromosome 22
Association studies of 33 single nucleotide polymorphisms (SNPs) in 29 candidate genes for bronchial asthma: positive association a T924C polymorphism in the thromboxane A2 receptor gene
Basic concepts in the study of diseases with complex genetics
CAPITALIZING ON LARGE-SCALE MOUSE MUTAGENESIS SCREENS
Chasing behaviour genes into the next millennium
Cloning, mapping and characterization of the human RAB27A gene
Complex patterns of intragenic polymorphism at the PDGFA locus
CYP17 polymorphism in the groups of distinct breast cancer susceptibility: comparison of patients with the bilateral disease vs. monolateral breast cancer patients vs. middle-aged female controls vs. elderly tumor-free women
Detection of Point Mutations on a DNA Microchip
Direct sequencing of bacterial and P1 artificial chromosome-nested deletions for identifying position-specific single-nucleotide polymorphisms
Estimation of Population Parameters and Recombination Rates From Single Nucleotide Polymorphisms
Genetic epidemiology of single-nucleotide polymorphisms
Genetic linkage in the estimation of pairwise relationship
Genetics of hypertension
High-throughput polymorphism screening and genotyping with high-density oligonucleotide arrays
Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population
Identification of 167 polymorphisms in 88 genes from candidate neurodegeneration pathways
Identification of 187 single nucleotide polymorphisms for ischemic heart disease in the Japanese population
Pharmacogenetics and the practice of medicine
Prediction of nonsynonymous single nucleotide polymorphisms in human disease-associated genes
Research suggests importance of haplotypes over SNPs
Single nucleotide polymorphism libraries: why and how are we building them?
SNPs: windows of opportunity in the human genome
Twenty SNPs and their allelic frequencies in four genes for familial long QT syndrome in Japanese population
SBE-TAGS- An array-based method for efficient single-nucleotide polymorphism genotyping
Search for DNA sequence variations using a MutS-based technology
Single-nucleotide polymorphism analysis by MALDI–TOF mass spectrometry
Species-specific nuclear and chloroplast single nucleotide polymorphisms
Strategies in complex disease mapping
The development of pharmacogenomic models to predict drug response
The genetics of complex diseases
The human caspase-activated DNase gene (hCAD): genomic structure, exonic single-nucleotide polymorphisms, and a highly polymorphic dincleotide repeat at the hCAD locus
Towards a structural basis of human non-synonymous single nucleotide polymorphisms
Using bioinformatics in gene and drug discovery
EST analysis online: WWW tools for detection of SNPs and alternative splice forms