Norikazu Sakamoto

Identification of a new point mutation in the human xanthine dehydrogenase gene responsible for a case of classical type I xanthinuria

Norikazu Sakamoto, Tetsuya Yamamoto, Yuji Moriwaki et al. · Human Genetics · 2001 · 41 citations

Mendelian Disorder, Classical Type, Genetic Disorder +7

Molecular structure of the Cβ catalytic subunit of rat cAMP-dependent protein kinase and differential expression of Cα and Cβ isoforms in rat tissues and cultured cells

Hisato Shuntoh, Norikazu Sakamoto, Shogo Matsuyama et al. · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 1992 · 17 citations

Signal Transduction, Molecular Physiology, Biochemistry +12

Relationship between mortality rate of stomach cancer and cerebrovascular disease and concentrations of magnesium and calcium in well water in Hyogo prefecture.

Norikazu Sakamoto, Motoki Shimizu, Ichiro Wakabayashi et al. · PubMed · 1997 · 16 citations

Stomach Cancer, Gastroenterology, Cerebrovascular Disease +17

Identification of a point mutation associated with a silent phenotype of human serum butyrylcholinesterase – a case of familial cholinesterasemia

Norikazu Sakamoto, Kazuo Hidaka, Takashi Fujisawa et al. · Clinica Chimica Acta · 1998 · 15 citations

Silent Phenotype, Mendelian Disorder, Genetic Disorder +6