H. Goto

发表

Molecular analysis of five independent Japanese mutant genes responsible for hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiency

Yasukazu Yamada, H. Goto, K. Suzumori, 1992, Human Genetics.

Molecular analysis of a Japanese family with Lesch‐Nyhan syndrome: identification of mutation and prenatal diagnosis

Y. Yamada, H. Goto, K. Suzumori, 1996, Clinical genetics.

Molecular genetic study of a Japanese family with Lesch-Nyhan syndrome: A point mutation at the consensus region of RNA splicing (HPRTKEIO)

Yasukazu Yamada, H. Goto, N. Ogasawara, 1993, Japanese Journal of Human Genetics.

Genetic study of pancreatic proteinase in mice (Mus musculus): Linkage of the Prt-2 locus on chromosome 8

Tomomasa Watanabe, H. Goto, N. Ogasawara, 1976, Biochemical Genetics.

Molecular analysis of extracellular-superoxide dismutase gene associated with high level in serum

K. Hirano, T. Adachi, Yasukazu Yamada, 1995, Japanese Journal of Human Genetics.

AMP deaminase isozymes in human tissues.

T. Watanabe, Y. Yamada, H. Goto, 1982, Biochimica et biophysica acta.

Identification of two independent Japanese mutant HPRT genes using the PCR technique.

Y. Yamada, H. Goto, N. Ogasawara, 1991, Advances in experimental medicine and biology.

Adenosine kinase from human liver.

Y. Yamada, H. Goto, N. Ogasawara, 1981, Biochimica et biophysica acta.

Isozymes of AMP deaminase.

T. Watanabe, H. Goto, N. Ogasawara, 1977, Advances in experimental medicine and biology.

AMP deaminase from rat brain: purification and characterization of multiple forms.

T. Watanabe, M. Yoshino, H. Goto, 1974, Biochimica et biophysica acta.

IMP dehydrogenase and action of antimetabolites in human cultured blast cells.

Y. Yamada, M. Yoshino, H. Goto, 1990, Biochimica et biophysica acta.

Phosphorylation of purine deoxynucleosides in human T- and B-lymphoblasts.

Y. Yamada, H. Goto, N. Ogasawara, 1986, Advances in experimental medicine and biology.

Deoxyguanosine kinase from human placenta.

Y. Yamada, H. Goto, N. Ogasawara, 1982, Biochimica et biophysica acta.

Differences of adenosine kinases from various mammalian tissues.

Y. Yamada, H. Goto, N. Ogasawara, 1982, Comparative biochemistry and physiology. B, Comparative biochemistry.

Genetic study of pancreatic proteinase in mice (Mus musculus): Genetic variants of trypsin and chymotrypsin

Tomomasa Watanabe, H. Goto, N. Ogasawara, 1976, Biochemical Genetics.

Purification and properties of adenosine kinase from rat brain.

Y. Yamada, H. Goto, N. Ogasawara, 1980, Biochimica et biophysica acta.

Three trypsinogens from rat pancreas

T. Watanabe, Y. Yamada, H. Goto, 1980, FEBS letters.

Purine nucleoside kinases in human T- and B-lymphoblasts.

Y. Yamada, H. Goto, N. Ogasawara, 1983, Biochimica et biophysica acta.

Distribution of AMP-deaminase isozymes in rat tissues.

T. Watanabe, Y. Yamada, H. Goto, 1978, European journal of biochemistry.

Distribution of AMP deaminase isozymes in various human blood cells.

T. Watanabe, Y. Yamada, H. Goto, 1984, The International journal of biochemistry.

Effects of various ligands on interaction of AMP deaminase with myosin.

Y. Yamada, H. Goto, N. Ogasawara, 1978, Biochimica et biophysica acta.

Multiple forms of AMP deaminase in various rat tissues

T. Watanabe, H. Goto, N. Ogasawara, 1974, FEBS letters.

AMP deaminase isozymes in rabbit red and white muscles and heart.

Y. Yamada, H. Goto, N. Ogasawara, 1983, Comparative biochemistry and physiology. B, Comparative biochemistry.

Gene mutations for human erythrocyte AMP deaminase deficiency.

Y. Yamada, H. Goto, N. Ogasawara, 1994, Advances in experimental medicine and biology.

Cloning and nucleotide sequence of the cDNA encoding human erythrocyte-specific AMP deaminase.

Y. Yamada, H. Goto, N. Ogasawara, 1992, Biochimica et biophysica acta.

Subunit structures of AMP deaminase isozymes in rat.

Y. Yamada, M. Yoshino, H. Goto, 1977, Biochemical and biophysical research communications.

Isozymes of rat AMP deaminase.

T. Watanabe, H. Goto, N. Ogasawara, 1975, Biochimica et biophysica acta.

Deficiency of AMP deaminase in erythrocytes

K. S. Park, Y. Yamada, H. Goto, 1987, Human Genetics.

Erythrocyte amp deaminase deficiency in Japanese: a compound heterozygote responsible for the complete deficiency.

Y. Yamada, H. Goto, N. Ogasawara, 2000, Advances in experimental medicine and biology.

Gene Mutations Responsible for Human Erythrocyte AMP Deaminase Deficiency in Poles

N. Nomura, H. Kitoh, Yasukazu Yamada, 1998 .

Complete deficiency of AMP deaminase in human erythrocytes.

Y. Yamada, H. Goto, N. Ogasawara, 1984, Biochemical and biophysical research communications.

Interaction of AMP deaminase with RNA.

Y. Yamada, H. Goto, N. Ogasawara, 1981, Biochimica et biophysica acta.

Isozymes of rat brain AMP deaminase: Developmental changes and characterizations of five forms

Tomomasa Watanabe, H. Goto, N. Ogasawara, 1975, FEBS letters.

Mutation in the gene encoding the fibroblast growth factor receptor‐3 in Korean children with achondroplasia

H. Kitoh, S. Yang, Yasukazu Yamada, 1998, Acta paediatrica Japonica : Overseas edition.

Partial hypoxanthine-guanine phosphoribosyl transferease deficiency in two Korean siblings—a new mutation

I. Ha, Yong Choi, J. Koo, 1993, Pediatric Nephrology.

Specific development of isocitrate dehydrogenases in rat brain

Tomomasa Watanabe, H. Goto, N. Ogasawara, 1974 .

AMP deaminase isozymes in human blood cells.

Y. Yamada, H. Goto, N. Ogasawara, 1984, Advances in experimental medicine and biology.

Deficiency of erythrocyte type isozyme of AMP deaminase in human.

Y. Yamada, H. Goto, N. Ogasawara, 1986 .

A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3

N. Wakamatsu, Y. Yamada, H. Goto, 2001, Human mutation.

DEFICIENCY OF ERYTHROCYTE TYPE ISOZYME OF AMP - DEAMINASE IN HUMAN: 148

Yasukazu Yamada, H. Goto, N. Ogasawara, 1985, Pediatric Research.

Molecular analysis of a female Lesch-Nyhan patient.

C. Caskey, J. T. Stout, H. Goto, 1989, The Journal of clinical investigation.

Identification of Mutations in the Gene Encoding the Fibroblast Growth Factor Receptor 3 in Japanese Patients with Achondroplasia

H. Kitoh, Yasukazu Yamada, H. Goto, 1995 .

Bilirubin: a potent inhibitor of NAD+-linked isocitrate dehydrogenase.

T. Watanabe, H. Goto, N. Ogasawara, 1973, Biochimica et biophysica acta.

GENETIC STUDY OF HEMOGLOBIN VARIANTS IN MICE (MUS MUSCULUS)

Tomomasa Watanabe, H. Goto, N. Ogasawara, 1976 .

Molecular basis for human erythrocyte AMP deaminase deficiency: screening for the major point mutation and identification of other mutations.

Y. Yamada, H. Goto, N. Ogasawara, 1994, Human Molecular Genetics.

A point mutation responsible for human erythrocyte AMP deaminase deficiency.

Y. Yamada, H. Goto, N. Ogasawara, 1994, Human Molecular Genetics.

Polymorphism of extracellular superoxide dismutase (EC-SOD) gene: relation to the mutation responsible for high EC-SOD level in serum

K. Hirano, S. Kakumu, A. Fukatsu, 1997, Japanese Journal of Human Genetics.

A Common Mutation in the Tyrosine Kinase Domain of the Fibroblast Growth Factor Receptor 3 Gene in Two Japanese Patients with Hypochondroplasia

H. Kitoh, Yasukazu Yamada, H. Goto, 1996 .