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几种错构瘤性息肉病的研究进展 被引量:8

Developent in the research of several kind of hamartomatous polyps
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出处 《中国实用内科杂志》 CAS CSCD 北大核心 2006年第5期663-664,共2页 Chinese Journal of Practical Internal Medicine
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参考文献9

  • 1Hearle N,Lucassen A,Wang R,et al.Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11 -negative PJS cases[J].Genes ChromosomesCancer,2004,41 (2):163-169.
  • 2Yashiro M,Kobayashi H,Kubo N,et al.Cronkhite-Canada syndrome containing colon cancer and serrated adenoma lesions[J].Digestion,2004,69 (1):57-62.
  • 3Mine S,Tanaka Y.One case of Cronkhite-Canada syndrome,in which the course from onset to spontaneous curing could be followed[J].J UOEH,2004,26 (2):245-251.
  • 4Ward EM,Wolfsen HC.Pharmacological management of Cronkhite-Canada syndrome[J].Expert Opin Pharmacother,2003,4 (3):385-389.
  • 5Fogt F,Brown CA,Badizadegan K,et al.Low prevalence of loss of heterozygosity and SMAD4 mutations in sporadic and familial juvenile polyposis syndrome-associated juvenile polyps[J].Am J Gastroenterol,2004,99 (10):2025-2031.
  • 6Brazowski E,Rosen P,Misonzhnick-Bedny F,et al.Characteristics of familial juvenile polyps expressing cyclooxygenase-2[J].Am J Gastroenterol,2005,100 (1):130-138.
  • 7Zhou XP,Waite KA,Pilarski R,et al.Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway[J].Am J Hum Genet,2003,73 (2):404-411.
  • 8Zhou XP,Woodford-Richens K,Lehtonen R,et al.Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes[J].Am J Hum Genet,2001,69 (4):704 -711.
  • 9Wirtzfeld DA,Petrelli NJ,Rodriguez-Bigas MA.Hamartomatous polyposis syndromes:molecular genetics,neoplastic risk,and surveillance recommendations[J].Ann Surg Oncol,2001,8 (4):319-327.

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