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Journal of the American Chemical Society|July 13, 2001
Catalytic enantioselective Reissert-type reaction: development and application to the synthesis of a potent NMDA receptor antagonist (-)-L-689,560 using a solid-supported catalystM Takamura, K Funabashi, M Kanai, et al.
Hinyokika Kiyo. Acta Urologica Japonica|March 1, 1996
[Multiple primary malignant neoplasms associated with genitourinary cancer]T Fukagai, M Ishihara, K Funabashi, et al.
Life Support & Biosphere Science : International Journal of Earth Space|September 7, 2001
Mineral recovery system for a Closed Ecology Experiment Facility (CEEF)H Kurokawa, K Funabashi, M Oda, et al.
Amino Acids|November 2, 2013
D-Aspartyl residue in a peptide can be liberated and metabolized by pig kidney enzymesY Kera, K Funabashi, T Matsumoto, et al.
Immunology|March 1, 1994
Tissue distribution of complement regulatory membrane proteins in ratsK Funabashi, N Okada, S Matsuo, et al.
Journal of Cardiovascular Pharmacology|January 1, 1992
In vitro biological profile of a highly potent novel endothelin (ET) antagonist BQ-123 selective for the ETA receptorM Ihara, K Ishikawa, T Fukuroda, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|August 1, 1996
[Expression of decay-accelerating factor on CD8-positive lymphocytes as an index of aging and of host defense function]Y Fuchino, N Okada, K Funabashi, et al.
Journal of Cardiovascular Pharmacology|January 1, 1991
Two endothelin receptor subtypes in porcine arteriesM Ihara, T Saeki, K Funabashi, et al.
Hinyokika Kiyo. Acta Urologica Japonica|May 1, 1994
[Usefulness of Dornier MPL9000 lithotriptor with new optional fluoroscopic guiding system (electrode X 155: depth 15.5cm) in treatment of urinary tract stone]T Saito, K Funabashi, T Kasahara, et al.
Chemical & Pharmaceutical Bulletin|December 1, 1992
Renin inhibitors. II. Synthesis and structure-activity relationships of N-terminus modified inhibitors containing a homostatine analogueS Atsuumi, M Nakano, Y Koike, et al.
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