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Results: 1-22 |
Results: 22
Progressive scoliosis in cri-du-chat syndrome over a 20-year follow-up period - A case report
Authors: Saito, N Ebara, S Fukushima, Y Wakui, K Takaoka, K
Citation: N. Saito et al., Progressive scoliosis in cri-du-chat syndrome over a 20-year follow-up period - A case report, SPINE, 26(7), 2001, pp. 835-837
Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses
Authors: Seki, H Kubota, T Ikegawa, S Haga, N Fujioka, F Ohzeki, S Wakui, K Yoshikawa, H Takaoka, K Fukushima, Y
Citation: H. Seki et al., Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses, AM J MED G, 99(1), 2001, pp. 59-62
Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1
Authors: Miyoshi, O Yabe, R Wakui, K Fukushima, Y Koizumi, S Uchikawa, M Kajii, T Numakura, C Takahashi, S Hayasaka, K Niikawa, N
Citation: O. Miyoshi et al., Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1, AM J MED G, 104(3), 2001, pp. 250-256
Domain-specific mutations of a transforming growth factor (TGF)-beta 1 latency-associated peptide cause Camurati-Engelmann disease because of the formation of a constitutively active form of TGF-beta 1
Authors: Saito, T Kinoshita, A Yoshiura, K Makita, Y Wakui, K Honke, K Niikawa, N Taniguchi, N
Citation: T. Saito et al., Domain-specific mutations of a transforming growth factor (TGF)-beta 1 latency-associated peptide cause Camurati-Engelmann disease because of the formation of a constitutively active form of TGF-beta 1, J BIOL CHEM, 276(15), 2001, pp. 11469-11472
Catalytic cracking of naphtha to light olefins
Authors: Yoshimura, Y Kijima, N Hayakawa, T Murata, K Suzuki, K Mizukami, F Matano, K Konishi, T Oikawa, T Saito, M Shiojima, T Shiozawa, K Wakui, K Sawada, G Sato, K Matsuo, S Yamaoka, N
Citation: Y. Yoshimura et al., Catalytic cracking of naphtha to light olefins, CATAL SURV, 4(2), 2000, pp. 157-167
An autosomal dominant posterior polar cataract locus maps to human chromosome 20pl 12-q12
Authors: Yamada, K Tomita, H Yoshiura, K Kondo, S Wakui, K Fukushima, Y Ikegawa, S Nakamura, Y Amemiya, T Niikawa, N
Citation: K. Yamada et al., An autosomal dominant posterior polar cataract locus maps to human chromosome 20pl 12-q12, EUR J HUM G, 8(7), 2000, pp. 535-539
Tocopherol affinity for serum lipoproteins of Japanese flounder Paralichthys olivaceus during the reproduction period
Authors: Tokuda, M Yamaguchi, T Wakui, K Sato, T Ito, M Takeuchi, M
Citation: M. Tokuda et al., Tocopherol affinity for serum lipoproteins of Japanese flounder Paralichthys olivaceus during the reproduction period, FISHERIES S, 66(4), 2000, pp. 619-624
Oxidative cracking of eta-butane over various silica packings
Authors: Wakui, K Satoh, KI Sawada, G Shiozawa, K Matano, KI Suzuki, K Hayakawa, T Murata, K Yoshimura, Y Mizukami, F
Citation: K. Wakui et al., Oxidative cracking of eta-butane over various silica packings, SEKIYU GAKK, 43(4), 2000, pp. 286-295
Analysis of nature of adsorption of hydrocarbons on rare earth-loaded HZSM-5 catalysts by pulse-injection method
Authors: Wakui, K Satoh, K Sawada, G Shiozawa, K Matano, K Suzuki, K Hayakawa, T Murata, K Yoshimura, Y Mizukami, F
Citation: K. Wakui et al., Analysis of nature of adsorption of hydrocarbons on rare earth-loaded HZSM-5 catalysts by pulse-injection method, SEKIYU GAKK, 43(3), 2000, pp. 218-224
Japanese family with an autosomal dominant chromosome instability syndrome: A new neurodegenerative disease?
Authors: Ishikawa, S Ishikawa, M Tokuda, T Yoshida, K Wakui, K Matsuura, S Ohara, S Sekijima, Y Hidaka, E Fukushima, Y Shigeta, H Komatsu, K Ikeda, S
Citation: S. Ishikawa et al., Japanese family with an autosomal dominant chromosome instability syndrome: A new neurodegenerative disease?, AM J MED G, 94(4), 2000, pp. 265-270
Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation
Authors: Ogata, T Wakui, K Kosho, T Muroya, K Yamanouchi, Y Takano, T Fukushima, Y Rappold, G Suzuki, Y
Citation: T. Ogata et al., Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation, AM J MED G, 92(4), 2000, pp. 256-259
Genetic evidence for a novel gene(s) involved in urogenital development on10q26
Authors: Ogata, T Muroya, K Sasagawa, I Kosho, T Wakui, K Sakazume, S Ito, K Matsuo, N Ohashi, H Nagai, T
Citation: T. Ogata et al., Genetic evidence for a novel gene(s) involved in urogenital development on10q26, KIDNEY INT, 58(6), 2000, pp. 2281-2290
Sex-determining gene(s) on distal 9p: Clinical and molecular studies in six cases
Authors: Muroya, K Okuyama, T Goishi, K Ogiso, Y Fukuda, S Kameyama, J Sato, H Suzuki, Y Terasaki, H Gomyo, H Wakui, K Fukushima, Y Ogata, T
Citation: K. Muroya et al., Sex-determining gene(s) on distal 9p: Clinical and molecular studies in six cases, J CLIN END, 85(9), 2000, pp. 3094-3100
Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature
Authors: Ogata, T Kosho, T Wakui, K Fukushima, Y Yoshimoto, M Miharu, N
Citation: T. Ogata et al., Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature, J CLIN END, 85(8), 2000, pp. 2927-2930
Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3
Authors: Ghadami, M Makita, Y Yoshida, K Nishimura, G Fukushima, Y Wakui, K Ikegawa, S Yamada, K Kondo, S Niikawa, N Tomita, H
Citation: M. Ghadami et al., Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3, AM J HU GEN, 66(1), 2000, pp. 143-147
Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies
Authors: Wakui, K Tanemura, M Suzumori, K Hidaka, E Ishikawa, M Kubota, T Fukushima, Y
Citation: K. Wakui et al., Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies, J HUM GENET, 44(2), 1999, pp. 85-90
Cyclodehydration of diethylene glycol (DEG) catalyzed by clay mineral sepiolite
Authors: Kitayama, Y Kamimura, M Wakui, K Kanamori, M Kodama, T Abe, J
Citation: Y. Kitayama et al., Cyclodehydration of diethylene glycol (DEG) catalyzed by clay mineral sepiolite, J MOL CAT A, 142(2), 1999, pp. 237-245
Scanning electron microscopy of desiccation-tolerant and -sensitive microspore-derived embryos of Brassica napus L.
Authors: Wakui, K Takahata, Y Kaizuma, N
Citation: K. Wakui et al., Scanning electron microscopy of desiccation-tolerant and -sensitive microspore-derived embryos of Brassica napus L., PL CELL REP, 18(7-8), 1999, pp. 595-600
Catalytic cracking of n-butane over rare earth-loaded HZSM-5 catalysts
Authors: Wakui, K Satoh, K Sawada, G Shiozawa, K Matano, K Suzuki, K Hayakawa, T Murata, K Yoshimura, Y Mizukami, F
Citation: K. Wakui et al., Catalytic cracking of n-butane over rare earth-loaded HZSM-5 catalysts, SEKIYU GAKK, 42(5), 1999, pp. 307-314
A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR
Authors: Kubota, T Nonoyama, S Tonoki, H Masuno, M Imaizumi, K Kojima, M Wakui, K Shimadzu, M Fukushima, Y
Citation: T. Kubota et al., A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR, HUM GENET, 104(1), 1999, pp. 49-55
Male sterility in alloplasmic Brassica rapa L. carrying Eruca sativa cytoplasm
Authors: Matsuzawa, Y Mekiyanon, S Kaneko, Y Bang, SW Wakui, K Takahata, Y
Citation: Y. Matsuzawa et al., Male sterility in alloplasmic Brassica rapa L. carrying Eruca sativa cytoplasm, PLANT BREED, 118(1), 1999, pp. 82-84
Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1
Authors: Tomita, H Nagamitsu, S Wakui, K Fukushima, Y Yamada, K Sadamatsu, M Masui, A Konishi, T Matsuishi, T Aihara, M Shimizu, K Hashimoto, K Mineta, M Matsushima, M Tsujita, T Saito, M Tanaka, H Tsuji, S Takagi, T Nakamura, Y Nanko, S Kato, N Nakane, Y Niikawa, N
Citation: H. Tomita et al., Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1, AM J HU GEN, 65(6), 1999, pp. 1688-1697
Risultati: 1-22 |