スポンサーリンク
Department of Neurology, Brain Research Institute, Niigata University | 論文
- Epidemiology of X-linked adrenoleukodystrophy in Japan
- Mutational Analysis of BRCA1 Gene in Ovarian and Breast-ovarian Cancer Families in Japan
- TDP-43 M337V Mutation in Familial Amyotrophic Lateral Sclerosis in Japan
- Appropriate data cleaning methods for genome-wide association study
- Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium
- Autosomal recessive juvenile parkinsonism
- Interaction of expanded polyglutamine stretches with nuclear transcription factors leads to aberrant transcriptional regulation in polyglutamine diseases
- Polyglutamine disease : Recent advances in the neuropathology of dentatorubral-pallidoluysian atrophy
- Genotype-phenotype correlation in CAG-repeat diseases
- Micrometer-Scale Photochromic Recording on Amorphous Diarylethene Film and Nondestructive Readout Using Near-Field IR Light
- Quantitative Evaluation of the Pyramidal Tract Segmented by Diffusion Tensor Tractography : Feasibility Study in Patients with Amyotrophic Lateral Sclerosis
- Haplotypes of BRCA1 Mutation Alleles in Japanese Ovarian and Breast-Ovarian Cancer Families: A Novel Method for Detecting BRCA1 Associated Ovarian Cancer
- Computational Evaluation of the Effects of Bone Ingrowth on Bone Resorptive Remodeling after a Cementless Total Hip Arthroplasty
- Numerical Analysis of Three-Dimensional Cervical Behaviors in Posterior-Oblique Car Collisions Using 3-D Human Whole Body Finite Element Model(Bioengineering)
- Uncemented Total Hip Replacement Stem Loosening after Long Term Compressive Stress Application : A Simulated FEA Study of Cortical Bone Remodeling(Bioengineering)
- Machado-Joseph disease gene products carrying different carboxyl termini
- Steroid-Responsive Limbic Encephalitis
- Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
- a-Si_O_x:H Films Prepared by Direct Photo-CVD Using CO_2 Gas : Condensed Matter
- MERRF/MELAS overlap syndrome associated with 3243 tRNA^mutation of mitochondrial DNA