スポンサーリンク
Gene Research Center, Tottori University | 論文
- Developmental Changes of Ni^ Sensitivity and Automaticity in Nkx2.5-Positive Cardiac Precursor Cells From Murine Embryonic Stem Cell
- State-Dependent Blocking Actions of Azimilide Dihydrochloride (NE-10064) on Human Cardiac Na^+ Channels
- Congenital myotonic dystrophy : report of paternal transmission
- Subtype Switching of T-Type Ca^ Channels From Cav3.2 to Cav3.1 During Differentiation of Embryonic Stem Cells to Cardiac Cell Lineage
- No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population
- Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism : A case-control study
- Serotonin transporter gene promoter polymorphism and autism : A family-based genetic association study in Japanese population
- No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population
- Gastrin-releasing peptide receptor (GRPR) locus in Japanese subjects with autism
- Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese
- Galactonojirimycin derivatives restore mutant human β-galactosidase activities expressed in fibroblasts from enzyme-deficient knockout mouse
- Increased NPC1 mRNA in skin fibroblasts from Niemann-Pick disease type C patients
- Novel TSC1 and TSC2 mutations in Japanese patients with tuberous sclerosis complex
- A novel interstitial deletion of KAL1 in a Japanese family with Kallmann syndrome
- Fibrillin gene (FBN1) mutations in Japanese patients with Marfan syndrome
- Absence of mutations in the β-catenin and adenomatous polyposis coli genes in papillary and follicular thyroid carcinomas
- Molecular Pathological Studies of Familial Amyotrophic Lateral Sclerosis
- 78 The Missense Mutation at the Cleavage Site of Insulin-like Growth Factor-I Receptor (arg709gln) in a Family with Short Stature Born Intrauterine Growth Retardation
- Effect of lactational exposure to 1, 2, 3, 4-tetrachlorodibenzo-p-dioxin on cytochrome P-450 1A1 mRNA in the neonatal rat liver: Quantitative analysis by the competitive RT-PCR method
- 19 A NOVEL NON-SENSE MUTATION IN ALSTROM SYNDROME : SUBCELLULAR LOCALIZATION OF ITS TRUNCATED PROTEIN