Yasuo Kagawa

A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)

Yoko Kobayashi, Mariko Y. Momoi, Kaoru Tominaga et al. · Biochemical and Biophysical Research Communications · 1990 · 372 citations

Life Sciences, Genetics, Molecular Genetics +17

Increased Uncoupling Protein2 mRNA in White Adipose Tissue, and Decrease in Leptin, Visceral Fat, Blood Glucose, and Cholesterol in KK-AyMice Fed with Eicosapentaenoic and Docosahexaenoic Acids in Addition to Linolenic Acid

Cha Seung Hun, Kyoko Hasegawa, Terue Kawabata et al. · Biochemical and Biophysical Research Communications · 1999 · 90 citations

Life Sciences, Endocrinology, Nutritional Sciences +17

Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy

Michisuke Yuzaki, Norio Ohkoshi, Ichiro Kanazawa et al. · Biochemical and Biophysical Research Communications · 1989 · 73 citations

Life Sciences, Genetics, Molecular Genetics +16

Complete cDNA encoding a putative phospholipase C from transformed human lymphocytes

Shigeo Ohta, Akira Matsui, Yoshinori Nazawa et al. · FEBS Letters · 1988 · 63 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +13

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

Jun-Ichi Hayashi, M Tanaka, Wataru Sato et al. · Biochemical and Biophysical Research Communications · 1990 · 46 citations

Life Sciences, Cell Biology, Molecular Biology +9