Nanba Eiji | Division Of Functional Genomics Research Center For Bioscience And Technology Tottori University

スポンサーリンク

概要

関連著者

もっと見る

著作論文

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
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?
Intracerebral cell transplantation therapy for murine GM1 gangliosidosis
Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome
A Cell Line Derived from Sphingomyelinosis Mouse Shows Alterations in Intracellular Cholesterol Metabolism Similar to Those in Type C Niemann-Pick Disease
Fibroblast screening for chaperone therapy in β-galactosidosis
Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers
Fragile X carrier screening and FMR1 allele distribution in the Japanese population
A case of galactosialidosis with a homozygous Q49R point mutation
Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn
Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
Altered Sensitivities to Potential Inhibitors of Cholesterol Biosynthesis in Niemann-Pick Type C Fibroblasts
Aberrant promoter methylation and expression of the imprinted PEG3 gene in glioma
Novel Mutations in the Gene Encoding Acid .ALPHA.-1,4-glucosidase in a Patient with Late-onset Glycogen Storage Disease Type II (Pompe Disease) with Impaired Intelligence
Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
Clinical and Serial MRI Findings of a Sialidosis Type I Patient with a Novel Missense Mutation in the NEU1 Gene
A Novel Mutation of the GAA Gene in a Patient with Adult-onset Pompe Disease Lacking a Disease-specific Pathology

もっと見る

スポンサーリンク