Important Reviews On Gene Therapy

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Important Reviews On SNP

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综合	方法	正常
疾病	药物	其它

　

分类

3150High-throughput genomics -snp
3166SNP mining

5074A SNPshot- pharmacogenetics and the future of drug therapy
4562Efficient Approach to Unique Single-Nucleotide Polymorphism Discovery
6826Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequences
6952Quality control in the discovery, reporting, and recording of genomic variation
6979Sampling SNPs
6313SNP frequencies in human genes
1945SNP-performance
1946SNP-pyrosequencing principle
5194SNPs; windows of opportunity in the human genome
5199The essence of SNPs
Species-specific nuclear and chloroplast single nucleotide polymorphisms
SNPs: windows of opportunity in the human genome
Single nucleotide polymorphism libraries: why and how are we building them?
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

4656Microplate array diagonal gel electrophoresis (MADGE), CpG-PCR and temporal thermal ramp-MADGE (Melt-MADGE) for single nucleotide analyses in populations
4667Multiplex detection of single-nucleotide variations using molecular beacons
5195SNP-tech
EST analysis online: WWW tools for detection of SNPs and alternative splice forms
Using bioinformatics in gene and drug discovery
Single-nucleotide polymorphism analysis by MALDI–TOF mass spectrometry
Search for DNA sequence variations using a MutS-based technology
SBE-TAGS- An array-based method for efficient single-nucleotide polymorphism genotyping
Research suggests importance of haplotypes over SNPs

6313SNP frequencies in human genes
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
Single nucleotide polymorphisms as tools in human genetics
Slow axonal transport: stop and go traffic in the axon
Towards a structural basis of human non-synonymous single nucleotide polymorphisms
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
Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population
High-throughput polymorphism screening and genotyping with high-density oligonucleotide arrays

4594Genetic Susceptibility to Atherosclerosis
6841How many diseases does it take to map a gene with SNPs
5445new insights into links between DNA polymerases, mutagenesis and human disease
Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases
Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory
The genetics of complex diseases
Strategies in complex disease mapping
Twenty SNPs and their allelic frequencies in four genes for familial long QT syndrome in Japanese population
Prediction of nonsynonymous single nucleotide polymorphisms in human disease-associated genes
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
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

	6131Making drug discovery a SNP 6998Somatic mutations and ageing 4790The use of single-nucleotide polymorphism maps in pharmacogenomics The development of pharmacogenomic models to predict drug response Pharmacogenetics and the practice of medicine

3165Single nucleotide polymorphism libraries 3665Mutation and Polymorphism Report -2000	7068Use of molecular variation in the NCBI dbSNP database Usefulness of Single Nucleotide Polymorphism Data for Estimating Population Parameters