Immunohistochemical differentiation between chronic enteropathy associated with SLCO2A1 gene and other inflammatory bowel diseases

논문상세정보

' Immunohistochemical differentiation between chronic enteropathy associated with SLCO2A1 gene and other inflammatory bowel diseases' 의 참고문헌

  • The 2nd edition of consensus statements for the diagnosis and management of intestinal Behcet's disease: indication of anti-TNFalpha monoclonal antibodies
    Hisamatsu T [2014]
  • Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis
    Diggle CP [2012]
  • Primary hypertrophic osteoarthropathy accompanied by Crohn's disease: a case report
    Shim YW [1997]
  • Non-specific multiple ulcers of the small intestine unrelated to non-steroidal antiinflammatory drugs
    Matsumoto T [2004]
  • Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing
    Busch J [2012]
  • Is hypertrophic osteoarthropathy really so rare in regional enteritis?
  • Historical review of so-called simple ulcer of the intestine
    Muto T [1979]
  • Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy
    Zhang Z [2012]
  • Evaluation of diagnostic criteria for Crohn's disease in Japan
    Hisabe T [2014]
  • Estrogen receptor status by immunohistochemistry is superior to the ligandbinding assay for predicting response to adjuvant endocrine therapy in breast cancer
    Harvey JM [1999]
  • Endoscopic therapy with absolute ethanol for postoperative recurrent ulcers in intestinal Behcet's disease, and simple ulcers
    Matsukawa M [2001]
  • Clinicopathologic features of chronic nonspecific multiple ulcers of the small intestine
    Esaki M [2015]
  • Chronic nonspecific multiple ulcers of the small intestine: a proposal of the entity from Japanese gastroenterologists to Western enteroscopists
    Matsumoto T [2007]
  • Chronic nonspecific multiple ulcer of the small intestine segregates in offspring from consanguinity
    Matsumoto T [2011]
  • Association of p53 protein expression with tumor cell proliferation rate and clinical outcome in node-negative breast cancer
    Allred DC [1993]
  • A new syndrome of Crohn's disease and pachydermoperiostosis in a family
    Compton RF [1997]
  • A hereditary enteropathy caused by mutations in the SLCO2A1 gene, encoding a prostaglandin transporter
    Umeno J [2015]