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Results: 1-25 | 26-43
Results: 1-25/43
Construction of 700 human/mouse A9 monochromosomal hybrids and analysis ofimprinted genes on human chromosome 6
Authors: Inoue, J Mitsuya, K Maegawa, S Kugoh, H Kadota, M Okamura, D Shinohara, T Nishihara, S Takehara, S Yamauchi, K Schulz, TC Oshimura, M
Citation: J. Inoue et al., Construction of 700 human/mouse A9 monochromosomal hybrids and analysis ofimprinted genes on human chromosome 6, J HUM GENET, 46(3), 2001, pp. 137-145
A novel in vitro system for analyzing parental allele-specific histone acetylation in genomic imprinting
Authors: Yoshioka, H Shirayoshi, Y Oshimura, M
Citation: H. Yoshioka et al., A novel in vitro system for analyzing parental allele-specific histone acetylation in genomic imprinting, J HUM GENET, 46(11), 2001, pp. 626-632
Germline transmission of a transferred human chromosome 21 fragment in transchromosomal mice
Authors: Kazuki, Y Shinohara, T Tomizuka, K Katoh, M Ohguma, A Ishida, I Oshimura, M
Citation: Y. Kazuki et al., Germline transmission of a transferred human chromosome 21 fragment in transchromosomal mice, J HUM GENET, 46(10), 2001, pp. 600-603
A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome
Authors: Meguro, M Kashiwagi, A Mitsuya, K Nakao, M Kondo, I Saitoh, S Oshimura, M
Citation: M. Meguro et al., A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome, NAT GENET, 28(1), 2001, pp. 19-20
Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes
Authors: Meguro, M Mitsuya, K Nomura, N Kohda, M Kashiwagi, A Nishigaki, R Yoshioka, H Nakao, M Oishi, M Oshimura, M
Citation: M. Meguro et al., Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes, HUM MOL GEN, 10(4), 2001, pp. 383-394
A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus
Authors: Arima, T Drewell, RA Arney, KL Inoue, J Makita, Y Hata, A Oshimura, M Wake, N Surani, MA
Citation: T. Arima et al., A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus, HUM MOL GEN, 10(14), 2001, pp. 1475-1483
Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome
Authors: Shinohara, T Tomizuka, K Miyabara, S Takehara, S Kazuki, Y Inoue, J Katoh, M Nakane, H Iino, A Ohguma, A Ikegami, S Inokuchi, K Ishida, I Reeves, RH Oshimura, M
Citation: T. Shinohara et al., Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome, HUM MOL GEN, 10(11), 2001, pp. 1163-1175
Functional evidence for a telomerase repressor gene on human chromosome 10p15.1
Authors: Nishimoto, A Miura, N Horikawa, I Kugoh, H Murakami, Y Hirohashi, S Kawasaki, H Gazdar, AF Shay, JW Barrett, JC Oshimura, M
Citation: A. Nishimoto et al., Functional evidence for a telomerase repressor gene on human chromosome 10p15.1, ONCOGENE, 20(7), 2001, pp. 828-835
Functional evidence for the presence of tumor suppressor gene on chromosome 10p15 in human prostate cancers
Authors: Fukuhara, H Maruyama, T Nomura, S Oshimura, M Kitamura, T Sekiya, T Murakami, Y
Citation: H. Fukuhara et al., Functional evidence for the presence of tumor suppressor gene on chromosome 10p15 in human prostate cancers, ONCOGENE, 20(3), 2001, pp. 314-319
Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma
Authors: Kohda, M Hoshiya, H Katoh, M Tanaka, I Masuda, R Takemura, T Fujiwara, M Oshimura, M
Citation: M. Kohda et al., Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma, MOL CARCINO, 31(4), 2001, pp. 184-191
Epigenetic silencing of PEG3 gene expression in human glioma cell lines
Authors: Maegawa, S Yoshioka, H Itaba, N Kubota, N Nishihara, S Shirayoshi, Y Nanba, E Oshimura, M
Citation: S. Maegawa et al., Epigenetic silencing of PEG3 gene expression in human glioma cell lines, MOL CARCINO, 31(1), 2001, pp. 1-9
Loss of imprinting of long QT intronic transcript 1 in colorectal cancer
Authors: Tanaka, K Shiota, G Meguro, M Mitsuya, K Oshimura, M Kawasaki, H
Citation: K. Tanaka et al., Loss of imprinting of long QT intronic transcript 1 in colorectal cancer, ONCOL-BASEL, 60(3), 2001, pp. 268-273
14-3-3 is involved in p75 neurotrophin receptor-mediated signal transduction
Authors: Kimura, MT Irie, S Shoji-Hoshino, S Mukai, J Nadano, D Oshimura, M Sato, TA
Citation: Mt. Kimura et al., 14-3-3 is involved in p75 neurotrophin receptor-mediated signal transduction, J BIOL CHEM, 276(20), 2001, pp. 17291-17300
Identification of a mutated DNA ligase IV gene in the X-ray-hypersensitivemutant SX10 of mouse FM3A cells
Authors: Sado, K Ayusawa, D Enomoto, A Suganuma, T Oshimura, M Sato, K Koyama, H
Citation: K. Sado et al., Identification of a mutated DNA ligase IV gene in the X-ray-hypersensitivemutant SX10 of mouse FM3A cells, J BIOL CHEM, 276(13), 2001, pp. 9742-9748
Preferential expression of an intact WRN gene in Werner syndrome cell lines in which a normal chromosome 8 has been introduced
Authors: Kashino, G Kodama, S Suzuki, K Oshimura, M Watanabe, M
Citation: G. Kashino et al., Preferential expression of an intact WRN gene in Werner syndrome cell lines in which a normal chromosome 8 has been introduced, BIOC BIOP R, 289(1), 2001, pp. 111-115
Epigenetic heterogeneity at imprinted loci in normal populations
Authors: Sakatani, T Wei, M Katoh, M Okita, C Wada, D Mitsuya, K Meguro, M Ikeguchi, M Ito, H Tycko, B Oshimura, M
Citation: T. Sakatani et al., Epigenetic heterogeneity at imprinted loci in normal populations, BIOC BIOP R, 283(5), 2001, pp. 1124-1130
Construction of human-rodent hybrid cells containing single transferable fragments of human chromosome 10p
Authors: Murakami, Y Uejima, H Fukuhara, H Maruyama, T Oshimura, M Sekiya, T
Citation: Y. Murakami et al., Construction of human-rodent hybrid cells containing single transferable fragments of human chromosome 10p, J HUM GENET, 45(6), 2000, pp. 370-373
Manipulation of human minichromosomes to carry greater than megabase-sizedchromosome inserts
Authors: Yoshimi, K Tomizuka, K Shinohara, T Kazuki, Y Yoshida, H Ohguma, A Yamamoto, T Tanaka, S Oshimura, M Ishida, I
Citation: K. Yoshimi et al., Manipulation of human minichromosomes to carry greater than megabase-sizedchromosome inserts, NAT BIOTECH, 18(10), 2000, pp. 1086-1090
Telomere shortening with aging in human liver
Authors: Takubo, K Nakamura, KI Izumiyama, N Furugori, E Sawabe, M Arai, T Esaki, Y Mafune, KI Kammori, M Fujiwara, M Kato, M Oshimura, M Sasajima, K
Citation: K. Takubo et al., Telomere shortening with aging in human liver, J GERONT A, 55(11), 2000, pp. B533-B536
Multipoint imprinting analysis in sporadic colorectal cancers with and without microsatellite instability
Authors: Nishihara, S Hayashida, T Mitsuya, K Schulz, TC Ikeguchi, M Kaibara, N Oshimura, M
Citation: S. Nishihara et al., Multipoint imprinting analysis in sporadic colorectal cancers with and without microsatellite instability, INT J ONCOL, 17(2), 2000, pp. 317-322
Mapping of metastasis suppressor genes for prostate cancer by microcell-mediated chromosome transfer
Authors: Ichikawa, T Hosoki, S Suzuki, H Akakura, K Igarashi, T Furuya, Y Oshimura, M Rinker-Schaeffer, CW Nihei, N Barrett, JC Isaacs, JT Ito, H
Citation: T. Ichikawa et al., Mapping of metastasis suppressor genes for prostate cancer by microcell-mediated chromosome transfer, ASIAN J AND, 2(3), 2000, pp. 167-171
Stability of transferred human chromosome fragments in cultured cells and in mice
Authors: Shinohara, T Tomizuka, K Takehara, S Yamauchi, K Katoh, M Ohguma, A Ishida, I Oshimura, M
Citation: T. Shinohara et al., Stability of transferred human chromosome fragments in cultured cells and in mice, CHROMOS RES, 8(8), 2000, pp. 713-725
Human monochromosome hybrid cell panel characterized by FISH in the JCRB/HSRRB
Authors: Tanabe, H Nakagawa, Y Minegishi, D Hashimoto, K Tanaka, N Oshimura, M Sofuni, T Mizusawa, H
Citation: H. Tanabe et al., Human monochromosome hybrid cell panel characterized by FISH in the JCRB/HSRRB, CHROMOS RES, 8(4), 2000, pp. 319-334
Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
Authors: Horike, S Mitsuya, K Meguro, M Kotobuki, N Kashiwagi, A Notsu, T Schulz, TC Shirayoshi, Y Oshimura, M
Citation: S. Horike et al., Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome, HUM MOL GEN, 9(14), 2000, pp. 2075-2083
Increased frequencies of gene and chromosome mutations after X-irradiationin mouse embryonal carcinoma cells transfected with the bcl-2 gene
Authors: Taga, M Shiraishi, K Shimura, T Uematsu, N Oshimura, M Niwa, O
Citation: M. Taga et al., Increased frequencies of gene and chromosome mutations after X-irradiationin mouse embryonal carcinoma cells transfected with the bcl-2 gene, JPN J CANC, 91(10), 2000, pp. 994-1000
Risultati: 1-25 | 26-43