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鳥取大学生命機能研究支援センター遺伝子探索 | 論文
- 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
- 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
- Antisense suppression of TSC1 gene product, hamartin, enhances neurite outgrowth in NGF-treated PC12h cells
- 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
- 自閉症の遺伝子解明の現状 (特集 発達障害の新たな遺伝子)
- A Cell Line Derived from Sphingomyelinosis Mouse Shows Alterations in Intracellular Cholesterol Metabolism Similar to Those in Type C Niemann-Pick Disease
- 大脳病変が半球性に急性発症、急性増悪を呈した Tay-Sachs 病の1幼児例
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