Search Results - "Migita, O."

  • Showing 1 - 9 results of 9
Refine Results
  1. 1

    An association between a missense polymorphism in the close homologue of L1 (CHL1, CALL) gene and schizophrenia by SAKURAI, K, MIGITA, O, TORU, M, ARINAMI, T

    Published in Molecular psychiatry (01-01-2002)
    “…Morphological alterations in the brains of schizophrenia patients suggest that neurodevelopmental dysfunction is involved in the etiology of the disease.(1)…”
    Get full text
    Journal Article
  2. 2

    Living‐Related Liver Transplantation for Siblings with Progressive Familial Intrahepatic Cholestasis 2, with Novel Genetic Findings by Shimizu, H., Migita, O., Kosaki, R., Kasahara, M., Fukuda, A., Sakamoto, S., Shigeta, T., Uemoto, S., Nakazawa, A., Kakiuchi, T., Arai, K.

    Published in American journal of transplantation (01-02-2011)
    “…Progressive familial intrahepatic cholestasis is a syndrome of severe cholestasis progressing to biliary cirrhosis and liver failure that develops in…”
    Get full text
    Journal Article
  3. 3

    Haplotype analysis of a 100 kb region spanning TNF-LTA identifies a polymorphism in the LTA promoter region that is associated with atopic asthma susceptibility in Japan by Migita, O., Noguchi, E., Koga, M., Jian, Z., Shibasaki, M., Migita, T., Ito, S., Ichikawa, K., Matsui, A., Arinami, T.

    Published in Clinical and experimental allergy (01-06-2005)
    “…Summary Background The tumour necrosis factor (TNF) gene family, which includes TNF, LTA, and LTB, is located consecutively on human chromosome 6p21 region,…”
    Get full text
    Journal Article
  4. 4
  5. 5

    Association of ZNF74 gene genotypes with age-at-onset of schizophrenia by Takase, K., Ohtsuki, T., Migita, O., Toru, M., Inada, T., Yamakawa-Kobayashi, K., Arinami, T.

    Published in Schizophrenia research (01-12-2001)
    “…Because of the manifestation of schizophrenic symptoms in individuals with interstitial deletions of chromosome 22q11.2, genes located in 22q11.2 are…”
    Get full text
    Journal Article
  6. 6

    Association of a haplotype block spanning SDAD1 gene and CXC chemokine genes with allergic rhinitis by Zhang, Jian, Noguchi, Emiko, Migita, Ohsuke, Yokouchi, Yukako, Nakayama, Junko, Shibasaki, Masanao, Arinami, Tadao

    Published in Journal of Allergy and Clinical Immunology (01-03-2005)
    “…Seasonal allergic rhinitis (SAR) is a common allergic disorder characterized by episodes of sneezing, rhinorrhea, and swelling of the nasal mucosa. Although…”
    Get full text
    Journal Article
  7. 7

    ADRB2 polymorphisms and asthma susceptibility: transmission disequilibrium test and meta-analysis by Migita, Ohsuke, Noguchi, Emiko, Jian, Zhang, Shibasaki, Masanao, Migita, Takuo, Ichikawa, Kunio, Matsui, Akira, Arinami, Tadao

    “…The beta(2)-adrenergic receptor (ADRB2) is the most common adrenergic receptor in the lung, and associations between ADRB2 polymorphisms and intermediate…”
    Get more information
    Journal Article
  8. 8
  9. 9

    Association between a polymorphism in cysteinyl leukotriene receptor 2 on chromosome 13q14 and atopic asthma by FUKAI, Hiromi, OGASAWARA, Yoshino, MIGITA, Ohsuke, KOGA, Minori, ICHIKAWA, Kunio, SHIBASAKI, Masanao, ARINAMI, Tadao, NOGUCHI, Emiko

    Published in Pharmacogenetics (London) (01-10-2004)
    “…Cysteinyl leukotriene receptor 2 (CYSLTR2) is one of the receptors for the cysteinyl leukotrienes (CYSLTs), which cause bronchoconstrictions, vascular…”
    Get full text
    Journal Article