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Items: 1 to 20 of 93

1.

Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes.

Forte G, Grossi V, Celestini V, Lucisano G, Scardapane M, Varvara D, Patruno M, Bagnulo R, Loconte D, Giunti L, Petracca A, Giglio S, Genuardi M, Pellegrini F, Resta N, Simone C.

BMC Cancer. 2014 Sep 11;14:661. doi: 10.1186/1471-2407-14-661.

2.

The FOXO3A rs2802292 G-allele associates with improved peripheral and hepatic insulin sensitivity and increased skeletal muscle-FOXO3A mRNA expression in twins.

Banasik K, Ribel-Madsen R, Gjesing AP, Wegner L, Andersson A, Poulsen P, Borglykke A, Witte DR, Pedersen O, Hansen T, Vaag A.

J Clin Endocrinol Metab. 2011 Jan;96(1):E119-24. doi: 10.1210/jc.2010-0881. Epub 2010 Sep 29.

PMID:
20881262
3.

Hamartomatous polyposis syndromes: molecular genetics, neoplastic risk, and surveillance recommendations.

Wirtzfeld DA, Petrelli NJ, Rodriguez-Bigas MA.

Ann Surg Oncol. 2001 May;8(4):319-27. Review.

PMID:
11352305
4.

Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.

Sweet K, Willis J, Zhou XP, Gallione C, Sawada T, Alhopuro P, Khoo SK, Patocs A, Martin C, Bridgeman S, Heinz J, Pilarski R, Lehtonen R, Prior TW, Frebourg T, Teh BT, Marchuk DA, Aaltonen LA, Eng C.

JAMA. 2005 Nov 16;294(19):2465-73.

PMID:
16287957
5.

The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

Schnitzler F, Friedrich M, Wolf C, Angelberger M, Diegelmann J, Olszak T, Beigel F, Tillack C, Stallhofer J, Göke B, Glas J, Lohse P, Brand S.

PLoS One. 2014 Nov 3;9(11):e108503. doi: 10.1371/journal.pone.0108503. eCollection 2014.

6.

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.

Resta N, Pierannunzio D, Lenato GM, Stella A, Capocaccia R, Bagnulo R, Lastella P, Susca FC, Bozzao C, Loconte DC, Sabbà C, Urso E, Sala P, Fornasarig M, Grammatico P, Piepoli A, Host C, Turchetti D, Viel A, Memo L, Giunti L, Stigliano V, Varesco L, Bertario L, Genuardi M, Lucci Cordisco E, Tibiletti MG, Di Gregorio C, Andriulli A, Ponz de Leon M; AIFEG.

Dig Liver Dis. 2013 Jul;45(7):606-11. doi: 10.1016/j.dld.2012.12.018. Epub 2013 Feb 15.

PMID:
23415580
7.

Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.

Stratakis CA, Kirschner LS, Taymans SE, Tomlinson IP, Marsh DJ, Torpy DJ, Giatzakis C, Eccles DM, Theaker J, Houlston RS, Blouin JL, Antonarakis SE, Basson CT, Eng C, Carney JA.

J Clin Endocrinol Metab. 1998 Aug;83(8):2972-6.

PMID:
9709978
8.

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.

9.

The hamartomatous polyposis syndromes: a clinical and molecular review.

Schreibman IR, Baker M, Amos C, McGarrity TJ.

Am J Gastroenterol. 2005 Feb;100(2):476-90. Review.

PMID:
15667510
10.

Genetics of the hamartomatous polyposis syndromes: a molecular review.

Chen HM, Fang JY.

Int J Colorectal Dis. 2009 Aug;24(8):865-74. doi: 10.1007/s00384-009-0714-2. Epub 2009 Apr 21. Review.

PMID:
19381654
11.

Germline variants in Hamartomatous Polyposis Syndrome-associated genes from patients with one or few hamartomatous polyps.

Jelsig AM, Brusgaard K, Hansen TP, Qvist N, Larsen M, Bojesen A, Nielsen CB, Ousager LB.

Scand J Gastroenterol. 2016 Sep;51(9):1118-25. doi: 10.1080/00365521.2016.1174880. Epub 2016 May 5.

PMID:
27146957
12.

Molecular and phenotypic markers of hamartomatous polyposis syndromes in the gastrointestinal tract.

Entius MM, Westerman AM, van Velthuysen ML, Wilson JH, Hamilton SR, Giardiello FM, Offerhaus GJ.

Hepatogastroenterology. 1999 Mar-Apr;46(26):661-6. Review.

PMID:
10370593
13.

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.

14.

Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood.

Achatz MI, Porter CC, Brugières L, Druker H, Frebourg T, Foulkes WD, Kratz CP, Kuiper RP, Hansford JR, Hernandez HS, Nathanson KL, Kohlmann WK, Doros L, Onel K, Schneider KW, Scollon SR, Tabori U, Tomlinson GE, Evans DGR, Plon SE.

Clin Cancer Res. 2017 Jul 1;23(13):e107-e114. doi: 10.1158/1078-0432.CCR-17-0790. Review.

15.

The association of FOXO3A gene polymorphisms with serum FOXO3A levels and oxidative stress markers in vitiligo patients.

Ozel Turkcu U, Solak Tekin N, Gokdogan Edgunlu T, Karakas Celik S, Oner S.

Gene. 2014 Feb 15;536(1):129-34. doi: 10.1016/j.gene.2013.11.055. Epub 2013 Dec 12.

PMID:
24333267
16.

Morphologic characterization of hamartomatous gastrointestinal polyps in Cowden syndrome, Peutz-Jeghers syndrome, and juvenile polyposis syndrome.

Shaco-Levy R, Jasperson KW, Martin K, Samadder NJ, Burt RW, Ying J, Bronner MP.

Hum Pathol. 2016 Mar;49:39-48. doi: 10.1016/j.humpath.2015.10.002. Epub 2015 Oct 31.

PMID:
26826408
17.

Association of the FOXO3A locus with extreme longevity in a southern Italian centenarian study.

Anselmi CV, Malovini A, Roncarati R, Novelli V, Villa F, Condorelli G, Bellazzi R, Puca AA.

Rejuvenation Res. 2009 Apr;12(2):95-104. doi: 10.1089/rej.2008.0827.

18.
19.

Genetic variation and human longevity.

Soerensen M.

Dan Med J. 2012 May;59(5):B4454.

PMID:
22549493
20.

Unwinding the heterogeneous nature of hamartomatous polyposis syndromes.

Carethers JM.

JAMA. 2005 Nov 16;294(19):2498-500. No abstract available.

PMID:
16287964

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