スポンサーリンク
Department of Molecular Biology-Institute of Gerontology, Nippon Medical School | 論文
- Association of natural tooth loss with genetic variation at the human matrix Gla protein locus in elderly women
- Association of the -381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss
- Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals
- Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene
- Genomic structure and chromosomal mapping of the human Site-1 protease (S1P) gene
- Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the SREBP cleavage-activating protein (SCAP) locus
- Molecular cloning and functional analysis of a factor that binds to the proximal promoter of human angiotensinogen
- A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density
- Association of bone mineral density with a dinucleotide repeat polymorphism at the calcitonin (CT) locus
- Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis
- Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia : A Molecular Study in an Eight-generation Hyperlipidemic Family
- Novel single nucleotide polymorphisms of the human nuclear factor kappa-B 2 gene identified by sequencing the entire gene
- Novel single nucleotide polymorphisms of the human colony-stimulating factor 2 (CSF2) gene identified by sequencing the entire gene
- Five novel single-nucleotide polymorphisms of human interferon gamma identified by sequencing the entire gene
- Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the human nuclear factor kappa-beta subunit 1 (NFKB1) locus
- Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities
- A novel LDLR mutation, H190Y, in a Utah kindred with familial Hypercholesterolemia
- Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) gene
- Human calcitonin receptor-like receptor for adrenomedullin : genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis
- 10) EXERCISE-INDUCED QRS CHANGES WITH MODIFIED FRANK'S LEAD