These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
123 related articles for article (PubMed ID: 21357597)
1. KILLIN gene discovery stirs up research on Cowden syndrome cancers. Schmidt C J Natl Cancer Inst; 2011 Mar; 103(5):362-4. PubMed ID: 21357597 [No Abstract] [Full Text] [Related]
2. Germline epigenetic regulation of KILLIN in Cowden and Cowden-like syndrome. Bennett KL; Mester J; Eng C JAMA; 2010 Dec; 304(24):2724-31. PubMed ID: 21177507 [TBL] [Abstract][Full Text] [Related]
3. PTEN promoter silencing and Cowden syndrome: the role of epigenetic regulation of KILLIN. Jelovac D; Park BH JAMA; 2010 Dec; 304(24):2744-5. PubMed ID: 21177512 [No Abstract] [Full Text] [Related]
4. Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma. Bennett KL; Campbell R; Ganapathi S; Zhou M; Rini B; Ganapathi R; Neumann HP; Eng C Genes Chromosomes Cancer; 2011 Aug; 50(8):654-61. PubMed ID: 21584899 [TBL] [Abstract][Full Text] [Related]
5. Germline PTEN, SDHB-D, and KLLN alterations in endometrial cancer patients with Cowden and Cowden-like syndromes: an international, multicenter, prospective study. Mahdi H; Mester JL; Nizialek EA; Ngeow J; Michener C; Eng C Cancer; 2015 Mar; 121(5):688-96. PubMed ID: 25376524 [TBL] [Abstract][Full Text] [Related]
6. A novel PTEN mutation in a Korean patient with Cowden syndrome and vascular anomalies. Bae BG; Kim HJ; Lee SG; Choi JR; Hwang C; Lee JH; Lee KA; Lee MG Acta Derm Venereol; 2011 Jan; 91(1):88-90. PubMed ID: 21103832 [No Abstract] [Full Text] [Related]
7. KLLN epigenotype-phenotype associations in Cowden syndrome. Nizialek EA; Mester JL; Dhiman VK; Smiraglia DJ; Eng C Eur J Hum Genet; 2015 Nov; 23(11):1538-43. PubMed ID: 25669429 [TBL] [Abstract][Full Text] [Related]
8. Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome. Pilarski R; Eng C J Med Genet; 2004 May; 41(5):323-6. PubMed ID: 15121767 [No Abstract] [Full Text] [Related]
9. How to recognize Cowden syndrome: A novel PTEN mutation description. Delannoy P; Debray FG; Verloes A; Beckers A; Valdes-Socin H Ann Endocrinol (Paris); 2017 Jul; 78(3):188-190. PubMed ID: 28262255 [No Abstract] [Full Text] [Related]
10. PTEN hamartoma tumor syndrome: clinical risk assessment and management protocol. Ngeow J; Eng C Methods; 2015 May; 77-78():11-9. PubMed ID: 25461771 [TBL] [Abstract][Full Text] [Related]
11. 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 Dis Colon Rectum; 2005 Sep; 48(9):1714-22. PubMed ID: 16007494 [TBL] [Abstract][Full Text] [Related]
12. Genetics of Cowden syndrome: through the looking glass of oncology. Eng C Int J Oncol; 1998 Mar; 12(3):701-10. PubMed ID: 9472113 [TBL] [Abstract][Full Text] [Related]
13. [Cowden disease and the PTEN gene: a successfully clinical and biological combined approach]. Longy M Bull Cancer; 2001 Dec; 88(12):1153-8. PubMed ID: 11792608 [TBL] [Abstract][Full Text] [Related]
14. Novel germline mutation of the PTEN gene in a Japanese family with Cowden disease. Harada N; Sugimura T; Yoshimura R; Motomura S; Shirahama S; Naramoto J; Chijiiwa Y; Nakamura K; Ito K; Nawata H J Gastroenterol; 2003; 38(1):87-91. PubMed ID: 12560928 [TBL] [Abstract][Full Text] [Related]
15. Cowden syndrome: a rare, but recognisable cancer predisposition disorder. Adlard JW Clin Oncol (R Coll Radiol); 2005 Aug; 17(5):393. PubMed ID: 16097574 [No Abstract] [Full Text] [Related]
16. PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol. Piccione M; Fragapane T; Antona V; Giachino D; Cupido F; Corsello G Am J Med Genet A; 2013 Nov; 161A(11):2902-8. PubMed ID: 24123798 [TBL] [Abstract][Full Text] [Related]
17. Cowden syndrome: what oncology nurses need to know about increased risk of developing certain cancers. Beamer LC Oncol Nurs Forum; 2014 Sep; 41(5):555-7. PubMed ID: 25158662 [TBL] [Abstract][Full Text] [Related]
18. A novel loss-of-function mutation (N48K) in the PTEN gene in a Spanish patient with Cowden disease. Vega A; Torres J; Torres M; Cameselle-Teijeiro J; Macia M; Carracedo A; Pulido R J Invest Dermatol; 2003 Dec; 121(6):1356-9. PubMed ID: 14675182 [TBL] [Abstract][Full Text] [Related]
19. Mutational abrogation of the PTEN/MMAC1 gene in gastrointestinal polyps in patients with Cowden disease. Chi SG; Kim HJ; Park BJ; Min HJ; Park JH; Kim YW; Dong SH; Kim BH; Lee JI; Chang YW; Chang R; Kim WK; Yang MH Gastroenterology; 1998 Nov; 115(5):1084-9. PubMed ID: 9797362 [TBL] [Abstract][Full Text] [Related]
20. A novel germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease. Sanson M; Zhou XP; Brault JL; Hoang-Xuan K; Hamelin R Acta Oncol; 1999; 38(7):973-5. PubMed ID: 10606430 [No Abstract] [Full Text] [Related] [Next] [New Search]