JSNP: a database of common gene variations in the Japanese population. - Wikidata - awgldk - TriplyDB

JSNP: a database of common gene variations in the Japanese population.

JSNP: a database of common gene variations in the Japanese population.

http://www.wikidata.org/entity/Q39524445

about

Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosis Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers Molecular analysis of a mutated FSH receptor detected in a patient with spontaneous ovarian hyperstimulation syndrome Extended linkage disequilibrium surrounding the hemoglobin E variant due to malarial selection Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetes VnD: a structure-centric database of disease-related SNPs and drugs Single nucleotide polymorphisms in Mycobacterium tuberculosis and the need for a curated database Association of the hCLCA1 gene with childhood and adult asthma Quantitative analysis of mitochondrial DNA 4977-bp deletion in sporadic breast cancer and benign breast diseases Assessing and managing risk when sharing aggregate genetic variant data PanSNPdb: the Pan-Asian SNP genotyping database A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1 PharmGKB: understanding the effects of individual genetic variants Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese A gentle introduction to SNP analysis: resources and tools.RExPrimer: an integrated primer designing tool increases PCR effectiveness by avoiding 3' SNP-in-primer and mis-priming from structural variation A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes.Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses WASP: a Web-based Allele-Specific PCR assay designing tool for detecting SNPs and mutations.Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD).PharmGKB: an integrated resource of pharmacogenomic data and knowledge.An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases.Mucin 1 gene (MUC1) and gastric-cancer susceptibility Association of TNFAIP3 polymorphism with susceptibility to systemic lupus erythematosus in a Japanese population.Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wi Replication study for the association between four Loci identified by a genome-wide association study on European American subjects with type 1 diabetes and susceptibility to diabetic nephropathy in Japanese subjects with type 2 diabetes.Associations between hOGG1 Ser326Cys polymorphism and increased body mass index and fasting glucose level in the Japanese general population.UASIS: Universal Automatic SNP Identification System.microPIR: an integrated database of microRNA target sites within human promoter sequences Genome-wide association study of coronary artery disease.Genetic aspects of stroke: human and experimental studies.An efficient and robust method for analyzing population pharmacokinetic data in genome-wide pharmacogenomic studies: a generalized estimating equation approach.Effects of lifestyle and single nucleotide polymorphisms on breast cancer risk: a case-control study in Japanese women.Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.How to build personalized multi-omics comorbidity profiles Pharmacogenomics in Japan.Genetic association between G protein-coupled receptor kinase 6/β-arrestin 2 and dopamine supersensitivity psychosis in schizophrenia Comprehensive literature review and statistical considerations for GWAS meta-analysis NABIC SNP: an integrated database for SNP markers An information-driven approach to pharmacogenomics.

P2860

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P2860

JSNP: a database of common gene variations in the Japanese population.

http://www.wikidata.org/entity/Q39524445

description

2002 nî lūn-bûn

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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2002年论文

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2002年论文

@zh-cn

name

JSNP: a database of common gene variations in the Japanese population.

@en

JSNP: a database of common gene variations in the Japanese population.

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type

label

JSNP: a database of common gene variations in the Japanese population.

@en

JSNP: a database of common gene variations in the Japanese population.

@nl

prefLabel

JSNP: a database of common gene variations in the Japanese population.

@en

JSNP: a database of common gene variations in the Japanese population.

@nl

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Nucleic Acids Research

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JSNP: a database of common gene variations in the Japanese population.

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P2093

Masako Kuroda

http://www.w3.org/2001/XMLSchema#string

Mika Hirakawa

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Toshihisa Takagi

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Yoichi Hashimoto

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Yusuke Nakamura

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P2860

The Sequence of the Human Genome

HGBASE: a database of SNPs and other variations in and around human genes

dbSNP: the NCBI database of genetic variation

Consed: a graphical tool for sequence finishing

Primer3 on the WWW for general users and for biologist programmers

RefSeq and LocusLink: NCBI gene-centered resources

Identification of protein coding regions by database similarity search

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

DNA data bank of Japan (DDBJ) in collaboration with mass sequencing teams

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158-162

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scholarly article

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10.1093/NAR/30.1.158

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1

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30

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Toshihiro Tanaka

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2002-01-01T00:00:00Z

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11605604

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11752280

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99126

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