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Nature Genetics|November 1, 1994
Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I geneH Ichinose, T Ohye, E Takahashi, et al.Japanese Journal of Cancer Research : Gann|April 1, 1997
Mutational analysis of BRCA1 gene in ovarian and breast-ovarian cancer families in JapanM Takano, H Aida, I Tsuneki, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin geneS Hayashi, K Wakabayashi, A Ishikawa, et al.American Journal of Medical Genetics|September 20, 1996
Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph diseaseK Endo, H Sasaki, A Wakisaka, et al.Journal of Neurochemistry|August 1, 1991
Incorporation of very-long-chain fatty acids into sphingolipids of cultured neural cellsM Saito, M SaitoJournal of Neuroscience Research|May 1, 1991
Monoclonal antibody Br4 recognizes specific neuronal cell typesM Saito, M SaitoJournal of Medical Virology|May 1, 1985
Unconventional pathogens causing spongiform encephalopathies absent in blood productsJ Tateishi, S TsujiNihon Rinsho. Japanese Journal of Clinical Medicine|September 1, 1993
[Positional cloning--current status and future directions]O Onodera, S TsujiJournal of the Neurological Sciences|February 1, 1986
Successful treatment of murine muscular dystrophy with the protease inhibitor bestatinS Tsuji, H MatsushitaPageof 737