Investigation of Japanese-specific alleles: Most are of Jomon lineage von Yuasa, Isao, Umetsu, Kazuo, Adachi, Noboru, Matsusue, Aya, Nakayashiki, Nori, Fujihara, Junko, Akane, Atsushi, Harihara, Shinji, Jin, Feng, Ishikawa, Takaki

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Wound age estimation by simultaneous detection of 9 cytokines in human dermal wounds with a multiplex bead-based immunoassay: An estimative method using outsourced examinations von Takamiya, Masataka, Biwasaka, Hitoshi, Saigusa, Kiyoshi, Nakayashiki, Nori, Aoki, Yasuhiro

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A hypervariable STR polymorphism in the CFI gene: Mutation rate and no linkage disequilibrium with FGA von Yuasa, Isao, Nakayashiki, Nori, Umetsu, Kazuo, Nishimukai, Hiroaki, Matsusue, Aya, Dewa, Koji

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Investigation of the methylation status around parent-of-origin detectable SNPs in imprinted genes von Nakayashiki, Nori, Takamiya, Masataka, Shimamoto, Kirito, Aoki, Yasuhiro, Hashiyada, Masaki

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A study on mRNA expressions of fibronectin in dermal and cerebral wound healing for wound age estimation von Takamiya, Masataka, Kumagai, Reiko, Nakayashiki, Nori, Aoki, Yasuhiro

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Hypothalamic transcript profiling in hypothermia using SuperSAGE von Takamiya, Masataka, MD, PhD, Nakayashiki, Nori, PhD, Dewa, Koji, MD, PhD

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A hypervariable STR polymorphism in the complement factor I (CFI) gene: Asian-specific alleles von Yuasa, Isao, Irizawa, Yoshito, Nishimukai, Hiroaki, Fukumori, Yasuo, Umetsu, Kazuo, Nakayashiki, Nori, Saitou, Naruya, Henke, Lotte, Henke, Jürgen

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Analysis of the methylation profiles in imprinted genes applicable to parental allele discrimination von Nakayashiki, Nori, Takamiya, Masataka, Shimamoto, Kirito, Aoki, Yasuhiro

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Systematic classification of alleles of the glycophorin A (MN blood group) gene von Mizukami, Hajime, Akane, Atsushi, Nakayashiki, Nori, Aoki, Yasuhiro, Shiono, Hiroshi

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A parent-of-origin detectable polymorphism in the hypermethylated region upstream of the human H19 gene von Nakayashiki, Nori, Kanetake, Jun, Aoki, Yasuhiro

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Multiplex amplified product-length polymorphism analysis for rapid detection of human mitochondrial DNA variations von Umetsu, Kazuo, Tanaka, Masashi, Yuasa, Isao, Saitou, Naruya, Takeyasu, Takeshi, Fuku, Noriyuki, Naito, Emiko, Ago, Kazutoshi, Nakayashiki, Nori, Miyoshi, Aya, Kashimura, Seiichi, Watanabe, Gotaro, Osawa, Motoki

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Allele frequencies of a SNP and a 27-bp deletion that are the determinant of earwax type in the ABCC11 gene von Kitano, Takashi, Yuasa, Isao, Yamazaki, Kentaro, Nakayashiki, Nori, Miyoshi, Aya, Park, Kyung Sook, Umetsu, Kazuo

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Sweat Protein Components Tested by SDS-Polyacrylamide Gel Electrophoresis Followed by Immunoblotting von NAKAYASHIKI, NORI

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An application of PCR-single strand conformation polymorphism to MN genotyping von Sasaki, Yoshitoshi, Nakayashiki, Nori, Saigusa, Kiyoshi, Takamiya, Masataka, Aoki, Yasuhiro

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Studies on differentially methylated parental allele in imprinted genes von Nakayashiki, Nori, Takamiya, Masataka, Shimamoto, Kirito, Aoki, Yasuhiro, Hashiyada, Masaki

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Investigation of SNP haplotypes in the H19 imprinted gene von Nakayashiki, Nori, Shimamoto, Kirito, Takamiya, Masataka, Hashiyada, Masaki, Yuasa, Isao, Dewa, Koji

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Suppression of experimental myasthenia gravis by monoclonal antibodies against MHC peptide region involved in presentation of a pathogenic T-cell epitope von Nakayashiki, Nori, Oshima, Minako, Deitiker, Philip R., Ashizawa, Tetsuo, Atassi, M.Zouhair

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Selective detection of parental alleles in imprinted gene, H19 von Nakayashiki, Nori, Kanetake, Jun, Takamiya, Masataka, Aoki, Yasuhiro

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A Case of a Newborn Infant with Hb M Iwate von KUMAGAI, REIKO, NIITSU, HISAE, KATSURA, IKUYO, NAKAYASHIKI, NORI, KATSURA, SYUSAKU

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ITIH1Q0iwate, a null allele of inter-alpha-trypsin inhibitor H1 caused by deletion/frameshift mutation von Nakayashiki, Nori, Ding, Mei, Umetsu, Kazuo, Yuasa, Isao, Suzuki, Tsuneo, Aoki, Yasuhiro

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