Variant manifestation of Cowden disease in Japan: hamartomatous polyposis of the digestive tract with mutation of the PTEN gene - PubMed (original) (raw)

Comment

Variant manifestation of Cowden disease in Japan: hamartomatous polyposis of the digestive tract with mutation of the PTEN gene

K Kurose et al. Am J Hum Genet. 1999 Jan.

No abstract available

PubMed Disclaimer

Comment on

• Molecular classification of the inherited hamartoma polyposis syndromes: clearing the muddied waters.
  Eng C, Ji H. Eng C, et al. Am J Hum Genet. 1998 May;62(5):1020-2. doi: 10.1086/301847. Am J Hum Genet. 1998. PMID: 9545417 Free PMC article. No abstract available.

Similar articles

• Analysis of PTEN gene mutations in Korean patients with Cowden syndrome and polyposis syndrome.
  Kim DK, Myung SJ, Yang SK, Hong SS, Kim KJ, Byeon JS, Lee GH, Kim JH, Min YI, Lee SM, Jeong JY, Song K, Jung SA. Kim DK, et al. Dis Colon Rectum. 2005 Sep;48(9):1714-22. doi: 10.1007/s10350-005-0130-9. Dis Colon Rectum. 2005. PMID: 16007494
• [Cowden disease and the PTEN gene: a successfully clinical and biological combined approach].
  Longy M. Longy M. Bull Cancer. 2001 Dec;88(12):1153-8. Bull Cancer. 2001. PMID: 11792608 Review. French.
• Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancer.
  Shugart YY, Cour C, Renard H, Lenoir G, Goldgar D, Teare D, Easton D, Rahman N, Gusterton R, Seal S, Barfoot R, Stratton M, Mangion J, Peelen T, van den Ouweland A, Meijers H, Devilee P, Eccles D, Lynch H, Weber B, Stoppa-Lyonnet D, Bignon YJ, Chang-Claude J. Shugart YY, et al. J Med Genet. 1999 Sep;36(9):720-1. J Med Genet. 1999. PMID: 10507734 Free PMC article. No abstract available.
• Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.
  Nelen MR, van Staveren WC, Peeters EA, Hassel MB, Gorlin RJ, Hamm H, Lindboe CF, Fryns JP, Sijmons RH, Woods DG, Mariman EC, Padberg GW, Kremer H. Nelen MR, et al. Hum Mol Genet. 1997 Aug;6(8):1383-7. doi: 10.1093/hmg/6.8.1383. Hum Mol Genet. 1997. PMID: 9259288
• [Cowden disease].
  Sawada T, Hamano N, Suzuki A, Okada T, Mabuchi H. Sawada T, et al. Nihon Rinsho. 2000 Jul;58(7):1479-83. Nihon Rinsho. 2000. PMID: 10921327 Review. Japanese.

Cited by

• Frequent loss of PTEN expression is linked to elevated phosphorylated Akt levels, but not associated with p27 and cyclin D1 expression, in primary epithelial ovarian carcinomas.
  Kurose K, Zhou XP, Araki T, Cannistra SA, Maher ER, Eng C. Kurose K, et al. Am J Pathol. 2001 Jun;158(6):2097-106. doi: 10.1016/S0002-9440(10)64681-0. Am J Pathol. 2001. PMID: 11395387 Free PMC article.
• Upper and Lower Gastrointestinal Findings in PTEN Mutation-Positive Cowden Syndrome Patients Participating in an Active Surveillance Program.
  Levi Z, Baris HN, Kedar I, Niv Y, Geller A, Gal E, Gingold R, Morgenstern S, Baruch Y, Leach BH, Bronner MP, Eng C. Levi Z, et al. Clin Transl Gastroenterol. 2011 Nov 17;2(11):e5. doi: 10.1038/ctg.2011.4. Clin Transl Gastroenterol. 2011. PMID: 23238744 Free PMC article.
• Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.
  Hendriks YM, Verhallen JT, van der Smagt JJ, Kant SG, Hilhorst Y, Hoefsloot L, Hansson KB, van der Straaten PJ, Boutkan H, Breuning MH, Vasen HF, Bröcker-Vriends AH. Hendriks YM, et al. Fam Cancer. 2003;2(2):79-85. doi: 10.1023/a:1025713815924. Fam Cancer. 2003. PMID: 14574156
• Protean PTEN: form and function.
  Waite KA, Eng C. Waite KA, et al. Am J Hum Genet. 2002 Apr;70(4):829-44. doi: 10.1086/340026. Epub 2002 Mar 1. Am J Hum Genet. 2002. PMID: 11875759 Free PMC article. Review.
• Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.
  Zhou XP, Woodford-Richens K, Lehtonen R, Kurose K, Aldred M, Hampel H, Launonen V, Virta S, Pilarski R, Salovaara R, Bodmer WF, Conrad BA, Dunlop M, Hodgson SV, Iwama T, Järvinen H, Kellokumpu I, Kim JC, Leggett B, Markie D, Mecklin JP, Neale K, Phillips R, Piris J, Rozen P, Houlston RS, Aaltonen LA, Tomlinson IP, Eng C. Zhou XP, et al. Am J Hum Genet. 2001 Oct;69(4):704-11. doi: 10.1086/323703. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536076 Free PMC article.

Publication types

MeSH terms

Substances

LinkOut - more resources

• Full Text Sources

  • Elsevier Science
  • Europe PubMed Central
  • PubMed Central

• Molecular Biology Databases

  • GlyGen glycoinformatics resource

• Research Materials

  • NCI CPTC Antibody Characterization Program