1991
上へ 1990 1991 1992 1993 1994 1995 1996 1997

Publications in 1991 from Otsuka Department of Clinical and Molecular Nutrition (ODCMN)

III.      PUBLICATIONS OF OTSUKA  DEPARTMENT OF CLINICAL
            AND MOLECULAR NUTRITION

1.       ORIGINAL PUBLICATIONS (ENGLISH)

7)              Katsuhiko Yoshimoto, Hiroyuki Iwahana, Katsuyuki Kubo, Shiro Saito, Mitsuo Itakura (1991) Allele Loss on Chromosome 11 in a Pituitary Tumor From a Patient with Multiple Endocrine Neoplasia Type I, Jpn. J. Cancer Res., 82, 886-889.

8)              Hiroyuki Iwahana, Katsuhiko Yoshimoto, Mitsuo Itakura  (1991) NcoI RFLP in the Human Prothrombin (F2) Gene. Nucleic Acids Res., 19(15), 4309.

9)              Mitsuo Itakura, Hiroko Yoshikawa, Chieko Bannai, Masako Kato, Kiyoshi Kunika, Yasushi Kawakami, Takashi Yamaoka, Kamejiro Yamashita (1991) Aminoguanidine Decreases Urinary Albumin and High-Molecular-Weight Proteins in Diabetic Rats. Life Sci., 49 (12), 889-897.

10)              Kiyoshi Kunika, Mitsuo Itakura, Kamejiro Yamashita  (1991) Correction of Fructosamine Value for Serum Albumin and Globulin Concentrations. Diabet. Res. Clin. Pr., 13, 37-44.

11)              Katsuyuki Kubo, Katsuhiko Yoshimoto, Yutaka Yokogoshi, Masaru Tsuyuguchi, Shiro Saito (1991) Loss of Heterozygosity on Chromosome 1p in Thyroid Adenoma and Medullary Carcinoma, but not in Papillary Carcinoma. Jpn. J. Cancer Res., 82, 1097-1103.

12)              Chihiro Nishimura, Takashi Yamaoka, Masakazu Mizutani, Kamejiro Yamashita, Tai Akera, Tsuyoshi Tanimoto (1991) Purification and Characterization of the Recombinant Human Aldose Reductase Expressed in Baculo Virus System. Biochim. Biophys. Acta., 1078, 171-178.

13)              Chihiro Nishimura, Yoshiharu Matsuura, Tsuyoshi Tanimoto, Takashi Yamaoka, Tai Akera, T. Geoffrey Flynn. (1991) cDNA Cloning and Expression of Human Aldose Reductase Expressed in Baculovirus System. Adv. Exp. Med. Biol., 284, 119-127.

14)              Setsuko Ii, Sharon Minnerath, Kunio Ii, Peter J. Dyck, Steve S. Sommer (1991) Two-Tired DNA-Based Diagnosis of Transthyretin Amyloidosis Reveals Two Novel Point Mutations. Neurol., 41(6), 893-898.

15)         Rhett P. Ketterling, Cynthia D. Bottema, Dwight D. Koeberl, Setsuko Ii, Steve S. Sommer (1991) T296M, a Common Mutation Causing Mild Hemophilia B in the Amish and Others: Founder Effect, Variability in Factor IX Activity Assays, and Rapid Carrier Detection. Hum. Genet., 87(3), 333-337.

16)              Cynthia D. Bottena, Rhett P. Ketterling, Setsuko Ii, Hon-Sup Yoon, John A. Phillips 3rd, Steve S. Sommer (1991) Missense Mutations and Evolutionary Conservation of Amino Acids: Evidence that Many of the Amino Acids in Factor IX Function as "Spacer" Elements. Am. J. Hum. Genet., 49(4), 820-838.

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