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Dna Link Inc. | 論文
- Single nucleotide polymorphisms and the haplotype in the DEFB1 gene are associated with atopic dermatitis in a Korean population
- Association analysis of sphingomyelinase 2 polymorphisms for the extrinsic type of atopic dermatitis in Koreans
- Replication of the Wellcome Trust genome-wide association study on essential hypertension in a Korean population
- Association analysis of signal transducer and activator of transcription 4 (STAT4) polymorphisms with asthma
- Association of eotaxin-2 gene polymorphisms with plasma eotaxin-2 concentration
- Interleukin 3 (IL3) polymorphisms associated with decreased risk of asthma and atopy
- Polymorphisms in interleukin 8 and its receptors (IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts
- Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women
- The molecular basis of phenylketonuria in Koreans
- Characterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean population
- Genetic interactions model among Eotaxin gene polymorphisms in asthma
- Polymorphisms in the leptin receptor (LEPR)-putative association with obesity and T2DM
- Identification and functional analysis of cystathionine beta-synthase gene mutations in patients with homocystinuria
- Association of single nucleotide polymorphisms in the IL-12 (IL-12A and B) and IL-12 receptor (IL-12Rβ1 and β2) genes and gene-gene interactions with atopic dermatitis in Koreans
- The Molecular Basis of Phenylketonuria in Koreans
- Identification of cartilage oligomeric matrix protein (COMP) gene mutations in patients with pseudoachondroplasia and multiple epiphyseal dysplasia
- Prevalence of congenital malformations and genetic diseases in Korea
- SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population
- Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality
- Single-nucleotide polymorphisms in the promoter of the CDK5 gene and lung cancer risk in a Korean population