W. Sato

发表

Mitochondrial mutation in fatal infantile cardiomyopathy

K. Ohno, T. Ozawa, Masashi Tanaka, 1990, The Lancet.

A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

K. Hayasaka, G. Takada, W. Sato, 1994, Biochemistry and molecular biology international.

Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin.

K. Hayasaka, E. Takahashi, M. Himoro, 1992, Biochemical and biophysical research communications.

Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin.

M. Tahara, K. Hayasaka, G. Takada, 1991, Biochemical and biophysical research communications.

Deletion of mitochondrial DNA in a patient with conduction block.

S. Sugiyama, K. Hattori, G. Takada, 1993, American heart journal.

Effects of ethidium bromide treatment of mouse cells on expression and assembly of nuclear-coded subunits of complexes involved in the oxidative phosphorylation.

Y. Kagawa, H. Yonekawa, J. Hayashi, 1990, Biochemical and biophysical research communications.

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiography

K. Harada, G. Takada, K. Hayasaka, 1993, Pediatric Cardiology.

Enzyme therapy in Gaucher disease type 2: an autopsy case.

H. Ida, Y. Yoshida, G. Takada, 1998, The Tohoku journal of experimental medicine.

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

T. Ozawa, Masashi Tanaka, Tomoko Yamamoto, 1991, Annals of neurology.

Isolation and sequence determination of cDNA encoding P2 protein of human peripheral myelin.

M. Tahara, K. Hayasaka, G. Takada, 1991, Biochemical and biophysical research communications.

Cardiomyopathy and angiopathy in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

T. Ozawa, S. Sugiyama, K. Harada, 1994, American heart journal.

Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

N. Shimizu, T. Bird, P. Chance, 1993, Nature Genetics.

Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy.

K. Ohno, T. Ozawa, S. Sugiyama, 1990, Biochemical and biophysical research communications.

Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence.

K. Ohno, T. Ozawa, Y. Mizuno, 1990, Biochemical and biophysical research communications.

Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

K. Hayasaka, G. Takada, W. Sato, 1993, Journal of Inherited Metabolic Disease.

Isolation of cDNA encoding the human liver phosphorylase kinase alpha subunit (PHKA2) and identification of a missense mutation of the PHKA2 gene in a family with liver phosphorylase kinase deficiency.

K. Hayasaka, G. Takada, W. Sato, 1995, Biochemistry and molecular biology international.

Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1

Y. Kuroda, K. Inui, T. Nishigaki, 1998, Journal of Inherited Metabolic Disease.

Acute life-threatening event with rhabdomyolysis after starting on high-dose pyridoxine therapy in an infant with homocystinuria

G. Takada, W. Sato, T. Takahashi, 1998, Journal of Inherited Metabolic Disease.

Mitochondrial DNA Mutations as an Etiology of Human Degenerative Diseases

K. Ohno, T. Ozawa, S. Sugiyama, 1990 .

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy.

K. Ohno, I. Nonaka, S. Horai, 1988, Biochemical and biophysical research communications.

Mitochondrial DNA Disease: Phylogeny and Expression

K. Ohno, T. Ozawa, M. Hayakawa, 1991 .

Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification method.

K. Ohno, T. Ozawa, M. Tanaka, 1989, Biochemical and biophysical research communications.

Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome.

K. Ohno, T. Ozawa, T. Negoro, 1991, Investigative ophthalmology & visual science.

Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

K. Hayasaka, G. Takada, Y. Sawaishi, 1992, American journal of human genetics.

Cytoplasmic body and mitochondrial DNA deletion

K. Ohno, T. Ozawa, Masashi Tanaka, 1990, Journal of the Neurological Sciences.

Types and mechanism of mitochondrial DNA mutations in mitochondrial myopathy and related diseases

K. Ohno, T. Ozawa, Masashi Tanaka, 1991 .

S1 Nuclease Analysis and Direct Sequencing of Deleted Mitochondrial DNA in Myopathic Patients: Role of Directly Repeated Sequences in Deletion

K. Ohno, T. Ozawa, Masashi Tanaka, 1990 .

Specific amplification of deleted mitochondrial DNA from a myopathic patient and analysis of deleted region with S1 nuclease.

K. Ohno, S. Horai, T. Ozawa, 1989, Biochimica et biophysica acta.

Direct sequencing of deleted mitochondrial DNA in myopathic patients.

K. Ohno, T. Ozawa, M. Tanaka, 1989, Biochemical and biophysical research communications.