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601.
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Mucopolysaccharidosis IVA: structural gene alterations identified by Southern blot analysis and identification of racial differences. [electronic resource] by
- Tomatsu, S
- Fukuda, S
- Cooper, A
- Wraith, J E
- Uchiyama, A
- Hori, T
- Nakashima, Y
- Yamada, N
- Sukegawa, K
- Kondo, N
Producer: 19950511
In:
Human genetics vol. 95
Availability: No items available.
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602.
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Autonomic regulation after exercise evidenced by spectral analysis of heart rate variability in asthmatic children. [electronic resource] by
- Fujii, H
- Fukutomi, O
- Inoue, R
- Shinoda, S
- Okammoto, H
- Teramoto, T
- Kondo, N
- Wada, H
- Saito, K
- Matsuoka, T
- Seishima, M
Producer: 20001026
In:
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology vol. 85
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603.
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Combined assessment of T-wave alternans and late potentials used to predict arrhythmic events after myocardial infarction. A prospective study. [electronic resource] by
- Ikeda, T
- Sakata, T
- Takami, M
- Kondo, N
- Tezuka, N
- Nakae, T
- Noro, M
- Enjoji, Y
- Abe, R
- Sugi, K
- Yamaguchi, T
Producer: 20000324
In:
Journal of the American College of Cardiology vol. 35
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604.
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p53-dependent hyperthermic enhancement of tumour growth inhibition by X-ray or carbon-ion beam irradiation. [electronic resource] by
- Takahashi, A
- Ota, I
- Tamamoto, T
- Asakawa, I
- Nagata, Y
- Nakagawa, H
- Kondo, N
- Ohnishi, K
- Furusawa, Y
- Matsumoto, H
- Ohnishi, T
Producer: 20030902
In:
International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group vol. 19
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605.
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Expression of multiple alpha1-antitrypsin-like genes in hibernating species of the squirrel family. [electronic resource] by
- Takamatsu, N
- Kojima, M
- Taniyama, M
- Ohba, K
- Uematsu, T
- Segawa, C
- Tsutou, S
- Watanabe, M
- Kondo, J
- Kondo, N
- Shiba, T
Producer: 19980212
In:
Gene vol. 204
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606.
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Ataxia telangiectasia associated with B-cell lymphoma: the effect of a half-dose of the drugs administered according to the acute lymphoblastic leukemia standard risk protocol. [electronic resource] by
- Yamada, Y
- Inoue, R
- Fukao, T
- Kaneko, H
- Isogai, K
- Fukuda, S
- Shimozawa, N
- Suzuki, Y
- Kondo, N
- Azuma, E
- Sakurai, M
Producer: 19990107
In:
Pediatric hematology and oncology vol. 15
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607.
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Roles of the primary cilium component Polaris in synchondrosis development. [electronic resource] by
- Ochiai, T
- Nagayama, M
- Nakamura, T
- Morrison, T
- Pilchak, D
- Kondo, N
- Hasegawa, H
- Song, B
- Serra, R
- Pacifici, M
- Koyama, E
Producer: 20090722
In:
Journal of dental research vol. 88
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608.
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Radiosensitivity of pimonidazole-unlabelled intratumour quiescent cell population to γ-rays, accelerated carbon ion beams and boron neutron capture reaction. [electronic resource] by
- Masunaga, S
- Sakurai, Y
- Tanaka, H
- Hirayama, R
- Matsumoto, Y
- Uzawa, A
- Suzuki, M
- Kondo, N
- Narabayashi, M
- Maruhashi, A
- Ono, K
Producer: 20130206
In:
The British journal of radiology vol. 86
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609.
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Epilepsy in peroxisomal diseases. [electronic resource] by
- Takahashi, Y
- Suzuki, Y
- Kumazaki, K
- Tanabe, Y
- Akaboshi, S
- Miura, K
- Shimozawa, N
- Kondo, N
- Nishiguchi, T
- Terada, K
- Orii, T
Producer: 19970319
In:
Epilepsia vol. 38
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610.
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Leaky phenotype of X-linked agammaglobulinaemia in a Japanese family. [electronic resource] by
- Kaneko, H
- Kawamoto, N
- Asano, T
- Mabuchi, Y
- Horikoshi, H
- Teramoto, T
- Matsui, E
- Kondo, M
- Fukao, T
- Kasahara, K
- Kondo, N
Producer: 20050726
In:
Clinical and experimental immunology vol. 140
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611.
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Novel exonic mutation (5319 G to A) resulting in two aberrantly spliced transcripts of the ATM gene in a Japanese patient with ataxia-telangiectasia. [electronic resource] by
- Fukao, T
- Tashita, H
- Teramoto, T
- Inoue, R
- Kaneko, H
- Komiyama, K
- Bar-Shira, A
- Gilad, S
- Shiloh, Y
- Nishimura, M
- Kondo, N
Producer: 19990630
In:
Human mutation vol. Suppl 1
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612.
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High and pointed type of femoral localized reaction frequently extends to complete and incomplete atypical femoral fracture in patients with autoimmune diseases on long-term glucocorticoids and bisphosphonates. [electronic resource] by
- Sato, H
- Kondo, N
- Nakatsue, T
- Wada, Y
- Fujisawa, J
- Kazama, J J
- Kuroda, T
- Suzuki, Y
- Nakano, M
- Endo, N
- Narita, I
Producer: 20180716
In:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA vol. 28
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613.
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Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case. [electronic resource] by
- Nagao-Watanabe, M
- Fukao, T
- Matsui, E
- Kaneko, H
- Inoue, R
- Kawamoto, N
- Kasahara, K
- Nagai, M
- Ichiki, Y
- Kitajima, Y
- Kondo, N
Producer: 20050308
In:
Clinical genetics vol. 66
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614.
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Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotype. [electronic resource] by
- Yamada, N
- Fukuda, S
- Tomatsu, S
- Muller, V
- Hopwood, J J
- Nelson, J
- Kato, Z
- Yamagishi, A
- Sukegawa, K
- Kondo, N
- Orii, T
Producer: 19980429
In:
Human mutation vol. 11
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615.
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The cumulative incidence of and risk factors for latent beaking in patients with autoimmune diseases taking long-term glucocorticoids and bisphosphonates. [electronic resource] by
- Sato, H
- Kondo, N
- Wada, Y
- Nakatsue, T
- Iguchi, S
- Fujisawa, J
- Kazama, J J
- Kuroda, T
- Nakano, M
- Endo, N
- Narita, I
Producer: 20161213
In:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA vol. 27
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616.
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Formation of the enzyme complex in mitochondria is required for function of trifunctional beta-oxidation protein. [electronic resource] by
- Orii, K E
- Aoyama, T
- Souri, M
- Jiang, L L
- Orii, K O
- Hayashi, S
- Yamaguchi, S
- Kondo, N
- Orii, T
- Hashimoto, T
Producer: 19960715
In:
Biochemical and biophysical research communications vol. 219
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617.
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Treatment of MPS VII (Sly disease) by allogeneic BMT in a female with homozygous A619V mutation. [electronic resource] by
- Yamada, Y
- Kato, K
- Sukegawa, K
- Tomatsu, S
- Fukuda, S
- Emura, S
- Kojima, S
- Matsuyama, T
- Sly, W S
- Kondo, N
- Orii, T
Producer: 19980527
In:
Bone marrow transplantation vol. 21
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618.
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Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders. [electronic resource] by
- Shimozawa, N
- Imamura, A
- Zhang, Z
- Suzuki, Y
- Orii, T
- Tsukamoto, T
- Osumi, T
- Fujiki, Y
- Wanders, R J
- Besley, G
- Kondo, N
Producer: 19991119
In:
Journal of medical genetics vol. 36
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619.
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PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p. [electronic resource] by
- Okumoto, K
- Shimozawa, N
- Kawai, A
- Tamura, S
- Tsukamoto, T
- Osumi, T
- Moser, H
- Wanders, R J
- Suzuki, Y
- Kondo, N
- Fujiki, Y
Producer: 19980716
In:
Molecular and cellular biology vol. 18
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620.
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D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder. [electronic resource] by
- Suzuki, Y
- Jiang, L L
- Souri, M
- Miyazawa, S
- Fukuda, S
- Zhang, Z
- Une, M
- Shimozawa, N
- Kondo, N
- Orii, T
- Hashimoto, T
Producer: 19971212
In:
American journal of human genetics vol. 61
Availability: No items available.
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