Sort by

Send to

Choose Destination

Links from PubMed

Items: 18


Genomic Biomarkers for Breast Cancer Risk.

Walsh MF, Nathanson KL, Couch FJ, Offit K.

Adv Exp Med Biol. 2016;882:1-32. doi: 10.1007/978-3-319-22909-6_1. Review.


Novel serine/threonine kinase 11 gene mutations in Peutz-Jeghers syndrome patients and endoscopic management.

Yajima H, Isomoto H, Nishioka H, Yamaguchi N, Ohnita K, Ichikawa T, Takeshima F, Shikuwa S, Ito M, Nakao K, Tsukamoto K, Kohno S.

World J Gastrointest Endosc. 2013 Mar 16;5(3):102-10. doi: 10.4253/wjge.v5.i3.102.


The differential diagnosis of familial lentiginosis syndromes.

Lodish MB, Stratakis CA.

Fam Cancer. 2011 Sep;10(3):481-90. doi: 10.1007/s10689-011-9446-x. Review.


Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.

Ausavarat S, Leoyklang P, Vejchapipat P, Chongsrisawat V, Suphapeetiporn K, Shotelersuk V.

World J Gastroenterol. 2009 Nov 14;15(42):5364-7.


Carney complex and lentiginosis.

Horvath A, Stratakis CA.

Pigment Cell Melanoma Res. 2009 Oct;22(5):580-7. doi: 10.1111/j.1755-148X.2009.00613.x. Epub 2009 Jul 24. Review.


Hamartomatous polyposis syndromes.

Gammon A, Jasperson K, Kohlmann W, Burt RW.

Best Pract Res Clin Gastroenterol. 2009;23(2):219-31. doi: 10.1016/j.bpg.2009.02.007. Review.


A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.

Thakur N, Reddy DN, Rao GV, Mohankrishna P, Singh L, Chandak GR.

BMC Med Genet. 2006 Sep 30;7:73.


STK11 status and intussusception risk in Peutz-Jeghers syndrome.

Hearle N, Schumacher V, Menko FH, Olschwang S, Boardman LA, Gille JJ, Keller JJ, Westerman AM, Scott RJ, Lim W, Trimbath JD, Giardiello FM, Gruber SB, Offerhaus GJ, Rooij FW, Wilson JH, Hansmann A, Möslein G, Royer-Pokora B, Vogel T, Phillips RK, Spigelman AD, Houlston RS.

J Med Genet. 2006 Aug;43(8):e41.


LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome.

Volikos E, Robinson J, Aittomäki K, Mecklin JP, Järvinen H, Westerman AM, de Rooji FW, Vogel T, Moeslein G, Launonen V, Tomlinson IP, Silver AR, Aaltonen LA.

J Med Genet. 2006 May;43(5):e18.


Cancer risks in LKB1 germline mutation carriers.

Mehenni H, Resta N, Park JG, Miyaki M, Guanti G, Costanza MC.

Gut. 2006 Jul;55(7):984-90. Epub 2006 Jan 11.


The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis.

Bauer AJ, Stratakis CA.

J Med Genet. 2005 Nov;42(11):801-10. Epub 2005 Jun 15. Review.


Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome.

Hearle NC, Tomlinson I, Lim W, Murday V, Swarbrick E, Lim G, Phillips R, Lee P, O'Donohue J, Trembath RC, Morrison PJ, Norman A, Taylor R, Hodgson S, Lucassen A, Houlston RS.

BMC Genomics. 2005 Mar 17;6:38.


LKB1, the multitasking tumour suppressor kinase.

Marignani PA.

J Clin Pathol. 2005 Jan;58(1):15-9. Review.


Genotype-phenotype correlations in Peutz-Jeghers syndrome.

Amos CI, Keitheri-Cheteri MB, Sabripour M, Wei C, McGarrity TJ, Seldin MF, Nations L, Lynch PM, Fidder HH, Friedman E, Frazier ML.

J Med Genet. 2004 May;41(5):327-33.


Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.

Lim W, Hearle N, Shah B, Murday V, Hodgson SV, Lucassen A, Eccles D, Talbot I, Neale K, Lim AG, O'Donohue J, Donaldson A, Macdonald RC, Young ID, Robinson MH, Lee PW, Stoodley BJ, Tomlinson I, Alderson D, Holbrook AG, Vyas S, Swarbrick ET, Lewis AA, Phillips RK, Houlston RS.

Br J Cancer. 2003 Jul 21;89(2):308-13.


Intussusceptions in a man with Peutz-Jeghers syndrome.

Marschall J, Hayes P.

CMAJ. 2003 Feb 4;168(3):315-6. No abstract available.


Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome.

Dunlop MG; British Society for Gastroenterology; Association of Coloproctology for Great Britain and Ireland.

Gut. 2002 Oct;51 Suppl 5:V21-7. No abstract available.

Items per page

Supplemental Content

Write to the Help Desk