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Life Sciences|February 10, 1999
Enterostatin (Val-Pro-Asp-Pro-Arg)-like immunoreactivity in rat urine: relationship to corticosterone outputM Imamura, A Prasad, C Prasad
Human Genetics|September 16, 1998
Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation patternT Ogata, K Wakui, K Muroya, et al.
Journal of Biochemistry|July 1, 1995
Morphology of ras-transformed cells becomes apparently normal again with tyrosine kinase inhibitors without a decrease in the ras-GTP complexH J Kwon, M Yoshida, K Muroya, et al.
Comparative Biochemistry and Physiology. C, Comparative Pharmacology and Toxicology|January 1, 1991
Interspecific variation in the emetic response of anuransT Naitoh, M Imamura, R J Wassersug
Nutritional Neuroscience|July 14, 2016
Differential Regional Distribution of Enterostatin, an Appetite Inhibiting Peptide, in the Brains of Zucker and Sprague-Dawley RatsM Imamura, J R Porter, C Prasad
Circulation Research|March 1, 1996
Activation of histamine H3-receptors inhibits carrier-mediated norepinephrine release during protracted myocardial ischemia. Comparison with adenosine A1-receptors and alpha2-adrenoceptorsM Imamura, H M Lander, R Levi
International Journal of Pancreatology : Official Journal of the International Association of Pancreatology|June 1, 1994
Effect of intraduodenal infusion of tocamphyl on pancreatic exocrine secretion and gastrointestinal hormone release in ratsM Imamura, H Yamauchi, W Y Chey
Life Sciences|June 10, 1998
Quantitative analysis of alpha-fetoprotein mRNA in circulating peripheral blood of patients with hepatocellular and alpha-fetoprotein-producing gastric carcinomasN O Funaki, J Tanaka, M Imamura
American Journal of Medical Genetics|June 8, 2000
Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlationT Ogata, K Wakui, T Kosho, et al.
American Journal of Medical Genetics|September 6, 1996
Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locusK Muroya, T Ogata, N Matsuo, et al.
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