スポンサーリンク
National Institute of Neuroscience, National Center of Neurology and Psychiatry | 論文
- Single Nucleotide Polymorphisms and Haplotypes of CYP1A2 in a Japanese Population
- Twenty-six Novel Single Nucleotide Polymorphisms and their Frequencies of the NR113 (CAR) Gene in a Japanese Population
- Eleven Novel Single Nucleotide Polymorphisms in the NR1I2 (PXR) Gene, Four of which Induce Non-synonymous Amino Acid Alterations
- The functional role of B7 molecules on the induction of thymocyte activation and apoptosis.
- The Functional Role of B7 Molecules on the Induction of Thymocyte Activation and Apoptosis
- Five Novel Single Nucleotide Polymorphisms in the EPHX1 Gene Encoding Microsomal Epoxide Hydrolase
- Dysferlinopathy associated with rigid spine syndrome
- Early head cooling in newborn piglets is neuroprotective even in the absence of profound systemic hypothermia
- A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom
- A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis
- Formation of Niobates from Aqueous Peroxide Solution
- 27aC03 Formation of lithium niobate from peroxide aqueous solution(NCCG-34)
- Optical and Electrical Studies on Trivalent-Ion (Cr, Fe)-Doped Potassium Titanyl Phosphate Single Crystals
- Vascular Endothelium Expresses 3-Mercaptopyruvate Sulfurtransferase and Produces Hydrogen Sulfide
- Photochemical Effects on Optical Properties of Molecular Contaminants
- Synthesis of TiO_2 Photo Catalysis Films on A2024 Alloy for Astronautics Applications by Sol-Gel Method
- Neuropathology of early-infantile epileptic encephalopathy with suppression-bursts ; comparison with those of early myoclonic encephalopathy and West syndrome
- Expression of Myoferlin in Skeletal Muscles of Patients with Dysferlinopathy
- Abnormality of cerebral gangliosides in Fukuyama type congenital muscular dystrophy
- Canine X-Linked Muscular Dystophy in Japan(CXMD_)