首页  癌症资讯  癌症常识  癌症症状  癌症预防  癌症诊断  癌症治疗  癌症护理  癌症药物  肿瘤医院  肿瘤专家  癌症问答
您现在的位置: 中国癌症预防网 >> 癌症常识 >> 正文
遗传性大肠癌
来源:中国癌症网     点击数:     更新时间:2007-4-20 22:27:36  
tly recognized syndrome. Surgery ,1974, 75:107–114.

[56] Jarvinen HJ, Fra ila KO. Familial juvenile polyposis coli: Increased risk of colorectal cancer. Gut ,1984, 25:792–800.

[57] Ja JR, Williams CB, Bu ey HJ, et al. Juvenile polyposis: a precancerous condition. Histopathology, 1988, 13: 619–30.

[58] Howe JR, Mitros FA, Summers RW. The risk of gastrointestinal carcinoma in familial juvenile polyposis. A Surg Oncol ,1998, 5:751–756.

[59] Scott-Co er CEH, Hausma M, Hall TJ, et al. Familial juvenile polyposis: pattern of recurrence and implication for surgical management. J Am Coll Surg ,1995, 181:407-413.

[60] Howe JR, Roth S, Ringold JC, et al. Mutatio in the SMAD4/DPC4 gene in juvenile polyposis. Science,1998, 280:1086–1088.

[61] Burger B, Uhlhaas S, Mangold E, et al. Novel de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis. Am J Med Genet ,2002,110: 289–91.

[62] Howe JR, Bair JL, Sayed MG, et al. Germline mutatio of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis. Nat Genet ,2001, 28:184–187.

[63] Sayed MG, Ahmed AF, Ringold JC, et al. Germline SMAD4 or BMPR1A mutatio and phenotype of juvenile polyposis. A Surg Oncol, 2002, 9(9):901–906.

[64] Haggitt RC, Reid BJ. Hereditary gastrointestinal polyposis syndromes. Am J Surg Pathol,1986, 10(12): 871- 887.

[65] Eng C. Cowden syndrome. J Genet Cou el ,1997, 6: 181–91. 20.

[66] Cohen MM. Ba ayan–Riley–Ruvalcaba syndrome: renaming three formerly recognized syndromes as one etiologic entity. Am J Med Genet ,1990, 35(2): 291–2.

[67] Zori RT, Marsh DJ, Graham GE, et al. Germline PTEN mutation in a family with Cowden syndrome and Ba ayan–Riley–Ruvalcaba syndrome. Am J Med Genet, 1998, 80(4): 399–402.

[68] Hendriks YMC, Verhallen JTCM, van der Smagt JJ, et al. Ba ayan–Riley–Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases. Familial Cancer ,2003, 2: 79–85.

[69] Liaw D, Marsh DJ, Li J , et al. Germline mutatio of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet ,1997, 16(1):64–67.

[70] Marsh DJ, Coulon V, Lunetta KL, et al. Mutation ectrum and genotype-phenotype analyses in Cowden disease and Ba ayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation. Hum Mol Genet, 1998 ,7(3):507-515.

[71] Marsh DJ, Kum JB, Lunetta KL, et al. PTEN mutation ectrum and genotype-phenotype correlatio in Ba ayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Hum Mol Genet, 1999, 8(8):1461-1472.

[72] Zhou XP, Loukola A, Salovaara R, et al. Germline PTEN promoter mutation and deletio in Cowden/ Ba ayan–Riley–Ruvalcaba syndrome results in aberrant PTEN protein and dysregulation of the pho hoinositol –3-kinase/Akt pathway. Am J Hum Gene, 2003.

来源转自:南方肿瘤中心网

上一页  [1] [2] [3] [4] [5] [6] [7] [8] [9] 

点 击 热 门