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Improvement of depth dose distribution using multiple-field irradiation in boron neutron capture therapy. [electronic resource] by
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- Tanaka, H
- Sakurai, Y
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- Kondo, N
- Narabayashi, M
- Nakagawa, Y
- Watanabe, T
- Kinashi, Y
- Masunaga, S
- Maruhashi, A
- Ono, K
- Suzuki, M
Producer: 20160909
In:
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine vol. 106
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642.
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Fifteen polymorphisms in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene: diagnostic implications in Morquio disease. [electronic resource] by
- Tomatsu, S
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- Cooper, A
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- Yamagishi, A
- Kato, Z
- Yamada, N
- Isogai, K
- Sukegawa, K
- Suzuki, Y
- Shimozawa, N
- Kondo, N
- Orii, T
Producer: 19990630
In:
Human mutation vol. Suppl 1
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643.
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The cell surface-expressed HSC70-like molecule preferentially reacts with the rat T-cell receptor Vdelta6 family. [electronic resource] by
- Kishi, A
- Ichinohe, T
- Hirai, I
- Kamiguchi, K
- Tamura, Y
- Kinebuchi, M
- Torigoe, T
- Ichimiya, S
- Kondo, N
- Ishitani, K
- Yoshikawa, T
- Kondo, M
- Matsuura, A
- Sato, N
Producer: 20011018
In:
Immunogenetics vol. 53
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644.
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Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans. [electronic resource] by
- Fukuda, S
- Shimozawa, N
- Suzuki, Y
- Zhang, Z
- Tomatsu, S
- Tsukamoto, T
- Hashiguchi, N
- Osumi, T
- Masuno, M
- Imaizumi, K
- Kuroki, Y
- Fujiki, Y
- Orii, T
- Kondo, N
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In:
American journal of human genetics vol. 59
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Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13. [electronic resource] by
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- Suzuki, Y
- Zhang, Z
- Imamura, A
- Tsukamoto, T
- Osumi, T
- Tateishi, K
- Okumoto, K
- Fujiki, Y
- Orii, T
- Barth, P G
- Wanders, R J
- Kondo, N
Producer: 19980327
In:
Biochemical and biophysical research communications vol. 243
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646.
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Evaluation of myocardial sympathetic nerve function in patients with mitral valve prolapse using iodine-123-metaiodobenzylguanidine myocardial scintigraphy. [electronic resource] by
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- Nomura, M
- Uemura, E
- Kageyama, N
- Kujime, S
- Kaji, M
- Noda, Y
- Kondo, N
- Kawaguchi, T
- Ozaki, Y
- Koshiba, K
- Yamaguchi, K
- Nakaya, Y
- Ito, S
Producer: 20080129
In:
Journal of medicine vol. 35
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647.
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Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency. [electronic resource] by
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- Fukao, T
- Mitchell, G A
- Kassovska-Bratinova, S
- Ugarte, M
- Wanders, R J
- Hirayama, K
- Shintaku, H
- Churchill, P
- Watanabe, H
- Orii, T
- Kondo, N
Producer: 19970519
In:
Biochimica et biophysica acta vol. 1360
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648.
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Autoantibodies to NMDA receptor in patients with chronic forms of epilepsia partialis continua. [electronic resource] by
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- Mori, H
- Mishina, M
- Watanabe, M
- Fujiwara, T
- Shimomura, J
- Aiba, H
- Miyajima, T
- Saito, Y
- Nezu, A
- Nishida, H
- Imai, K
- Sakaguchi, N
- Kondo, N
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In:
Neurology vol. 61
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649.
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ATM is upregulated during the mitogenic response in peripheral blood mononuclear cells. [electronic resource] by
- Fukao, T
- Kaneko, H
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- Gatei, M
- Tashita, H
- Yoshida, T
- Cross, S
- Kedar, P
- Watters, D
- Khana, K K
- Misko, I
- Kondo, N
- Lavin, M F
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650.
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Association between interleukin-18 gene polymorphism 105A/C and asthma. [electronic resource] by
- Higa, S
- Hirano, T
- Mayumi, M
- Hiraoka, M
- Ohshima, Y
- Nambu, M
- Yamaguchi, E
- Hizawa, N
- Kondo, N
- Matsui, E
- Katada, Y
- Miyatake, A
- Kawase, I
- Tanaka, T
Producer: 20031204
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651.
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Mucopolysaccharidosis IVA: submicroscopic deletion of 16q24.3 and a novel R386C mutation of N-acetylgalactosamine-6-sulfate sulfatase gene in a classical Morquio disease. [electronic resource] by
- Fukuda, S
- Tomatsu, S
- Masuno, M
- Ogawa, T
- Yamagishi, A
- Rezvi, G M
- Sukegawa, K
- Shimozawa, N
- Suzuki, Y
- Kondo, N
- Imaizumi, K
- Kuroki, Y
- Okabe, T
- Orii, T
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In:
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Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiency. [electronic resource] by
- Tomatsu, S
- Fukuda, S
- Yamagishi, A
- Cooper, A
- Wraith, J F
- Hori, T
- Kato, Z
- Yamada, N
- Isogai, K
- Sukegawa, K
- Kondo, N
- Suzuki, Y
- Shimozawa, N
- Orii, T
Producer: 19960725
In:
American journal of human genetics vol. 58
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653.
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D-bifunctional protein deficiency with fetal ascites, polyhydramnios, and contractures of hands and toes. [electronic resource] by
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- Zhang, Z
- Shimozawa, N
- Kondo, N
- Ishii, N
- Funatsuka, M
- Shirakawa, S
- Itoh, M
- Takashima, S
- Une, M
- Kana-aki, R R
- Mukai, K
- Osawa, M
- Suzuki, Y
Producer: 20020125
In:
The Journal of pediatrics vol. 139
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Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy. [electronic resource] by
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- Teramoto, T
- Tashita, H
- Shimozawa, N
- Nishimura, M
- Asano, T
- Oda, M
- Kamei, A
- Ishiguro, H
- Kato, S
- Ohashi, T
- Kobayashi, H
- Eto, Y
- Kondo, N
Producer: 20010111
In:
Journal of inherited metabolic disease vol. 23
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655.
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Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations. [electronic resource] by
- Rezvi, G M
- Tomatsu, S
- Fukuda, S
- Yamagishi, A
- Cooper, A
- Wraith, J E
- Iwata, H
- Kato, Z
- Yamada, N
- Sukegawa, K
- Shimozawa, N
- Suzuki, Y
- Kondo, N
- Orii, T
Producer: 19961122
In:
Journal of inherited metabolic disease vol. 19
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656.
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Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts. [electronic resource] by
- Shimozawa, N
- Suzuki, Y
- Zhang, Z
- Imamura, A
- Kondo, N
- Kinoshita, N
- Fujiki, Y
- Tsukamoto, T
- Osumi, T
- Imanaka, T
- Orii, T
- Beemer, F
- Mooijer, P
- Dekker, C
- Wanders, R J
Producer: 19990201
In:
American journal of human genetics vol. 63
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657.
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Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient. [electronic resource] by
- Kassovska-Bratinova, S
- Fukao, T
- Song, X Q
- Duncan, A M
- Chen, H S
- Robert, M F
- Pérez-Cerdá, C
- Ugarte, M
- Chartrand, C
- Vobecky, S
- Kondo, N
- Mitchell, G A
Producer: 19960925
In:
American journal of human genetics vol. 59
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658.
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Positional cloning of the gene for Nijmegen breakage syndrome. [electronic resource] by
- Matsuura, S
- Tauchi, H
- Nakamura, A
- Kondo, N
- Sakamoto, S
- Endo, S
- Smeets, D
- Solder, B
- Belohradsky, B H
- Der Kaloustian, V M
- Oshimura, M
- Isomura, M
- Nakamura, Y
- Komatsu, K
Producer: 19980701
In:
Nature genetics vol. 19
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659.
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Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia. [electronic resource] by
- Yoshida, N
- Sakaguchi, H
- Muramatsu, H
- Okuno, Y
- Song, C
- Dovat, S
- Shimada, A
- Ozeki, M
- Ohnishi, H
- Teramoto, T
- Fukao, T
- Kondo, N
- Takahashi, Y
- Matsumoto, K
- Kato, K
- Kojima, S
Producer: 20180614
In:
Leukemia vol. 31
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660.
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Evaluation of accumulated mucopolysaccharides in the brain of patients with mucopolysaccharidoses by (1)H-magnetic resonance spectroscopy before and after bone marrow transplantation. [electronic resource] by
- Takahashi, Y
- Sukegawa, K
- Aoki, M
- Ito, A
- Suzuki, K
- Sakaguchi, H
- Watanabe, M
- Isogai, K
- Mizuno, S
- Hoshi, H
- Kuwata, K
- Tomatsu, S
- Kato, S
- Ito, T
- Kondo, N
- Orii, T
Producer: 20010712
In:
Pediatric research vol. 49
Availability: No items available.
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