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The Japanese Journal of Human Genetics|June 1, 1996
A common mutation in methylenetetrahydrofolate reductase gene among the Japanese populationH Nishio, M J Lee, M Fujii, et al.
Archives of Toxicology|January 29, 2000
Itai-itai disease is not associated with polymorphisms of the estrogen receptor alpha geneH Nishio, C Hayashi, M J Lee, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Two cases of a renal epithelial tumour resembling immature nephronY Nagashima, N Arai, Y Tanaka, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology|January 1, 1990
Establishment of an epithelioid malignant schwannoma cell line (YST-1)Y Nagashima, Y Ohaki, Y Tanaka, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 16, 1999
Detection of mutations in the COL4A5 gene in over 90% of male patients with X-linked Alport's syndrome by RT-PCR and direct sequencingY Inoue, H Nishio, T Shirakawa, et al.
Journal of Virology|May 30, 1998
Induction of systemic and mucosal immune responses to human immunodeficiency virus type 1 by a DNA vaccine formulated with QS-21 saponin adjuvant via intramuscular and intranasal routesS Sasaki, K Sumino, K Hamajima, et al.
Journal of Neurology|February 13, 1999
High incidence of a survival motor neuron gene/cBCD541 gene ratio of 2 in Japanese parents of spinal muscular atrophy patients: a characteristic background of spinal muscular atrophy in Japan?H Nishio, Y Ishikawa, M J Lee, et al.
Human Mutation|April 29, 1998
A novel single basepair insertion in exon 6 of the Bruton's tyrosine kinase (Btk) gene from a Japanese X-linked agammaglobulinemia patient with growth hormone insufficiencyK Abo, H Nishio, M J Lee, et al.
Ryumachi. [Rheumatism]|February 1, 1995
[Optic neuropathy in systemic lupus erythematosus (SLE)--analysis of 54 cases including our case]T Igarashi, Y Ishigatsubo, K Motoji, et al.
The Kobe Journal of Medical Sciences|September 14, 2000
Prenatal diagnosis of a Japanese family at risk for Tay-Sachs disease. Application of a fluorescent competitive allele-specific polymerase chain reaction (PCR) methodS Tamasu, H Nishio, H Ayaki, et al.
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