Sakai Norio | Department Of Developmental Medicine (pediatrics) D-5 Osaka University Graduate School Of Medicine.

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著作論文

The C-Terminal Region of Serotonin Transporter Is Important for Its Trafficking and Glycosylation
Analysis of the stable levels of messenger RNA derived from different polymorphic alleles in the vitamin D receptor gene
Fragmentation of Protein Kinase N (PKN) in the Hydrocephalic Rat Brain
Antiepileptic Effects of Single and Repeated Oral Administrations of S-312-d, a Novel Calcium Channel Antagonist, on Tonic Convulsions in Spontaneously Epileptic Rats
Perospirone, a Novel Antipsychotic Agent, Hyperpolarizes Rat Dorsal Raphe Neurons via 5-HT_ Receptor
IV F10 Abnormal excitability of hippocampal CA3 pyramidal neurons involving abnormal Ca2^+ activity in Noda epileptic rats
Congo Red, an Amyloid-Inhibiting Compound, Alleviates Various Types of Cellular Dysfunction Triggered by Mutant Protein Kinase Cγ That Causes Spinocerebellar Ataxia Type 14 (SCA14) by Inhibiting Oligomerization and Aggregation
Sleep disordered breathing in childhood-onset acid maltase deficiency
Hereditary hypophosphatemic rickets with hypercalciuria : a study for the phosphate transporter gene type IIc and osteoblastic function
Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia : New Understanding
Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss
Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome
Six novel mutations detected in the GALC gene in 17 Japanese patients with Krabbe disease, and new genotype-phenotype correlation
A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency
Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease
Hormonal and Genetical Assessment of a Japanese Girl with Weaver Syndrome
Involvement of Ca^ Channels in Abnormal Excitability of Hippocampal CA3 Pyramidal Cells in Noda Epileptic Rats
A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period
Effects of D-Fraction, a Polysaccharide from Grifola frondosa on Tumor Growt Involve Activation of NK Cells
Computational Analysis of Molecular Recognition in DNA Base-Sequence and Groove by Methidium Chloride Using Molecular Mechanics Calculation
Electrophysiological Characterization of Nicotine-Induced Excitaiton of Dopaminergic Neurons in the Rat Substantia Nigra
Spatiotemporal Analysis of the Molecular Interaction between PICK1 and PKC
Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome
Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates
Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
A Patient with Sotos Syndrome Who Reached Final Height
136 Excessive Growth in a Japanese Girl with Weaver Syndrome
Theoretical Relation between Spatial Resolution and Efficiency of Detection in Scanning Hot Electron Microscope
Shortening of Detection Time for Observation of Hot Electron Spatial Distribution by Scanning Hot Electron Microscopy
A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia
Elucidation of the Molecular Mechanism and Exploration of Novel Therapeutics for Spinocerebellar Ataxia Caused by Mutant Protein Kinase Cγ
Congo Red, an Amyloid-Inhibiting Compound, Alleviates Various Types of Cellular Dysfunction Triggered by Mutant Protein Kinase Cγ That Causes Spinocerebellar Ataxia Type 14 (SCA14) by Inhibiting Oligomerization and Aggregation

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