Search Results - "Ouchida, M."

Refine Results
  1. 1

    Oesophageal squamous cell carcinoma may develop within a background of accumulating DNA methylation in normal and dysplastic mucosa by Ishii, T, Murakami, J, Notohara, K, Cullings, H M, Sasamoto, H, Kambara, T, Shirakawa, Y, Naomoto, Y, Ouchida, M, Shimizu, K, Tanaka, N, Jass, J R, Matsubara, N

    Published in Gut (01-01-2007)
    “…Background: Oesophageal squamous cell carcinoma (OSCC) often arises from preceding dysplastic lesions in the oesophageal epithelium. However, the molecular…”
    Get full text
    Journal Article
  2. 2

    Severity dependent up-regulations of LOX-1 and MCP-1 in early sclerotic changes of common carotid arteries in spontaneously hypertensive rats by Hamakawa, Y., Omori, N., Ouchida, M., Nagase, M., Sato, K., Nagano, I., Shoji, M., Fujita, T., Abe, K.

    Published in Neurological research (New York) (01-10-2004)
    “…Lectin-like oxidized low-density lipoprotein receptor (LOX-1) and monocyte chemoattractant protein-1 (MCP-1) are molecules involving in the initiation and…”
    Get full text
    Journal Article
  3. 3
  4. 4

    Prognostic value of loss of heterozygosity around three candidate tumor suppressor genes on chromosome 10q in astrocytomas by TERADA, Kinya, TAMIYA, Takashi, SHIMIZU, Kenji, DAIDO, Shigeru, KAMBARA, Hirokazu, TANAKA, Hiroaki, ONO, Yasuhiro, MATSUMOTO, Kengo, ITO, Sachio, OUCHIDA, Mamoru, OHMOTO, Takashi

    Published in Journal of neuro-oncology (01-06-2002)
    “…We thoroughly examined loss of heterozygosity (LOH) around three candidate tumor suppressor genes on chromosome 10q to determine whether LOH of each tumor…”
    Get full text
    Journal Article
  5. 5
  6. 6
  7. 7
  8. 8

    Measurement of ω mesons via radiative decay mode in = 200 GeV Au+Au collisions at RHIC-PHENIX by Ouchida, M.

    Published in Indian journal of physics (2011)
    “…We report on ω mesons’ production via radiative decay mode ( ω → π 0 γ , π 0 → 2 γ ) in = 200 GeV Au+Au collisions at RHIC-PHENIX. The main difficulty of this…”
    Get full text
    Journal Article
  9. 9

    Detection of EGFR Gene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay by ASANO, Hiroaki, TOYOOKA, Shinichi, HIRAKI, Akio, SUGI, Kazuro, KIURA, Katsuyuki, DATE, Hiroshi, SHIMIZU, Nobuyoshi, TOKUMO, Masaki, ICHIMURA, Kouichi, AOE, Keisuke, ITO, Sachio, TSUKUDA, Kazunori, OUCHIDA, Mamoru, AOE, Motoi, KATAYAMA, Hideki

    Published in Clinical cancer research (01-01-2006)
    “…Purpose: Mutations in the epidermal growth factor receptor ( EGFR ) gene have been reported to be present in non–small cell lung cancer (NSCLC) and related to…”
    Get full text
    Journal Article
  10. 10

    Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy by Ohmori, Iori, Ouchida, Mamoru, Ohtsuka, Yoko, Oka, Eiji, Shimizu, Kenji

    “…To investigate the possible correlation between genotype and phenotype of epilepsy, we analyzed the voltage-gated sodium channel α1-subunit (SCN1A) gene,…”
    Get full text
    Journal Article
  11. 11
  12. 12
  13. 13
  14. 14

    Aberrant promoter methylation of human DAB2 interactive protein (hDAB2IP) gene in lung cancers by Yano, Masaaki, Toyooka, Shinichi, Tsukuda, Kazunori, Dote, Hideaki, Ouchida, Mamoru, Hanabata, Tetsuro, Aoe, Motoi, Date, Hiroshi, Gazdar, Adi F., Shimizu, Nobuyoshi

    Published in International journal of cancer (01-01-2005)
    “…The human DOC‐2/DAB2 interactive protein gene (hDAB2IP) is a novel member of the Ras GTPase‐activating gene family that is known to act as a tumor suppressor…”
    Get full text
    Journal Article
  15. 15

    Single nucleotide polymorphism in fibroblast growth factor receptor 4 at codon 388 is associated with prognosis in high‐grade soft tissue sarcoma by Morimoto, Yuki, Ozaki, Toshifumi, Ouchida, Mamoru, Umehara, Norifumi, Ohata, Norihide, Yoshida, Aki, Shimizu, Kenji, Inoue, Hajime

    Published in Cancer (15-11-2003)
    “…BACKGROUND A recent study revealed that single nucleotide polymorphism (SNP) at codon 388 (Gly or Arg) of fibroblast growth factor receptor 4 (FGFR4) was…”
    Get full text
    Journal Article
  16. 16

    Significant growth suppression of synovial sarcomas by the histone deacetylase inhibitor FK228 in vitro and in vivo by Ito, Tatsuo, Ouchida, Mamoru, Morimoto, Yuki, Yoshida, Aki, Jitsumori, Yoshimi, Ozaki, Toshifumi, Sonobe, Hiroshi, Inoue, Hajime, Shimizu, Kenji

    Published in Cancer letters (28-06-2005)
    “…About 97% of synovial sarcomas harbor the SYT– SSX fusion gene by chromosomal translocation. We found that the histone deacetylase (HDAC) inhibitor FK228…”
    Get full text
    Journal Article
  17. 17

    Aberrant Promoter Methylation in Human DAB2 Interactive Protein (hDAB2IP) Gene in Breast Cancer by DOTE, Hideaki, TOYOOKA, Shinichi, SHIMIZU, Nobuyoshi, TSUKUDA, Kazunori, YANO, Masaaki, OUCHIDA, Mamoru, DOIHARA, Hiroyoshi, SUZUKI, Makoto, CHEN, Hong, HSIEH, Jer-Tsong, GAZDAR, Adi F

    Published in Clinical cancer research (15-03-2004)
    “…Purpose: Human DOC-2/DAB2 interactive protein ( hDAB2IP ) gene is a novel member of the Ras GTPase-activating family and has been demonstrated to be a tumor…”
    Get full text
    Journal Article
  18. 18

    Establishment and characterization of a biphasic synovial sarcoma cell line, SYO-1 by Kawai, Akira, Naito, Noriko, Yoshida, Aki, Morimoto, Yuki, Ouchida, Mamoru, Shimizu, Kenji, Beppu, Yasuo

    Published in Cancer letters (10-02-2004)
    “…We describe here the establishment of a new synovial sarcoma cell line, SYO-1, derived from a biphasic synovial sarcoma that developed in the groin of a…”
    Get full text
    Journal Article
  19. 19

    Minimally invasive direct coronary artery bypass for ischemic heart disease associated with preoperative severe complications by Isomura, T, Sato, R, Hayashida, N, Ouchida, M, Watanabe, S

    “…Our experiences of minimally invasive direct coronary artery bypass (MIDCAB) were reported with review of literatures. Patient #1 was a 69 years-old man with…”
    Get more information
    Journal Article
  20. 20

    Genomic structure of the human ING1 gene and tumor-specific mutations detected in head and neck squamous cell carcinomas by GUNDUZ, M, OUCHIDA, M, FUKUSHIMA, K, HANAFUSA, H, ETANI, T, NISHIOKA, S, NISHIZAKI, K, SHIMIZU, K

    Published in Cancer research (Chicago, Ill.) (15-06-2000)
    “…We characterized the genomic structure of the human ING1 gene, a candidate tumor suppressor gene, and found that the gene has three exons. We also demonstrated…”
    Get full text
    Journal Article