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Division Of Functional Genomics Research Center For Bioscience And Technology Tottori University | 論文
- FRS-053 Distinct Role of Hsp70 and Hsc70 in Wild-type hERG Maturation Processing(FRS11,New Insights into Basic Mechanisms of Arrhythmia (A),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- ガングリオシド蓄積症とシグナル伝達 (特集 脳と糖脂質)
- アストロサイトのオートファジーとmTOR (特集 mTORをめぐるシグナルタンパク)
- 遺伝子診断の実際 (特大号/先天代謝異常症--日常診療で必須の知識) -- (診断の進歩)
- 末梢血泡沫細胞と頭部MRIでの髄鞘化遅延を認めたGM1ガングリオシドーシスの1例
- 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
- FRS-091 Impairment of Ubiquitin-Proteasome System Caused by a Missense MYBPC3 Mutation and Associated with Cardiac Dysfunction in Hypertrophic Cardiomyopathy(FRS19,Genetic Abnormalities in Cardiac Hypertrophy and Cardiomyopathy (M),Featured Research Sessi
- 1 Role of the Ubiquitin Proteasome System in the Development of Heart Failure in Hypertrophic Cardiomyopathy(Young Investigator's Award for International Students Finalists Lecture (YIA International),Special Program,The 72nd Annual Scientific Meeting of
- Subtype Switching of T-Type Ca^ Channels From Cav3.2 to Cav3.1 During Differentiation of Embryonic Stem Cells to Cardiac Cell Lineage
- Characteristic findings of auditory brainstem response and otoacoustic emission in the Bronx waltzer mouse
- 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
- Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin : A new syndrome?
- Allele Frequency of Human Endothelial Nitric Oxide Synthase Gene Polymorphism in Abdominal Aortic Aneurysm
- Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese
- Clinical Evaluation of Breech Deliveries Over a Fifteen-Year Period at a Hospital in Ota, Japan
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