BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

272 related articles for article (PubMed ID: 23415580)

  • 1. 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;
    Dig Liver Dis; 2013 Jul; 45(7):606-11. PubMed ID: 23415580
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome.
    Connolly DC; Katabuchi H; Cliby WA; Cho KR
    Am J Pathol; 2000 Jan; 156(1):339-45. PubMed ID: 10623683
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.
    Wang ZJ; Churchman M; Avizienyte E; McKeown C; Davies S; Evans DG; Ferguson A; Ellis I; Xu WH; Yan ZY; Aaltonen LA; Tomlinson IP
    J Med Genet; 1999 May; 36(5):365-8. PubMed ID: 10353780
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers.
    Su GH; Hruban RH; Bansal RK; Bova GS; Tang DJ; Shekher MC; Westerman AM; Entius MM; Goggins M; Yeo CJ; Kern SE
    Am J Pathol; 1999 Jun; 154(6):1835-40. PubMed ID: 10362809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11.
    Trojan J; Brieger A; Raedle J; Roth WK; Zeuzem S
    Am J Gastroenterol; 1999 Jan; 94(1):257-61. PubMed ID: 9934767
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma.
    Guldberg P; thor Straten P; Ahrenkiel V; Seremet T; Kirkin AF; Zeuthen J
    Oncogene; 1999 Mar; 18(9):1777-80. PubMed ID: 10208439
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
    Kruse R; Uhlhaas S; Lamberti C; Keller KM; Jackisch C; Steinhard J; Knöpfle G; Loff S; Back W; Stolte M; Jungck M; Propping P; Friedl W; Jenne DE
    Hum Mutat; 1999; 13(3):257-8. PubMed ID: 10090485
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Peutz-Jeghers syndrome: a new understanding.
    Choi HS; Park YJ; Park JG
    J Korean Med Sci; 1999 Feb; 14(1):2-7. PubMed ID: 10102516
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Peutz-Jeghers syndrome].
    Miyaki M
    Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer.
    Bignell GR; Barfoot R; Seal S; Collins N; Warren W; Stratton MR
    Cancer Res; 1998 Apr; 58(7):1384-6. PubMed ID: 9537235
    [TBL] [Abstract][Full Text] [Related]  

  • 11. High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.
    Papp J; Kovacs ME; Solyom S; Kasler M; Børresen-Dale AL; Olah E
    BMC Med Genet; 2010 Nov; 11():169. PubMed ID: 21118512
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours.
    Wang ZJ; Churchman M; Campbell IG; Xu WH; Yan ZY; McCluggage WG; Foulkes WD; Tomlinson IP
    Br J Cancer; 1999 Apr; 80(1-2):70-2. PubMed ID: 10389980
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.
    Westerman AM; Entius MM; Boor PP; Koole R; de Baar E; Offerhaus GJ; Lubinski J; Lindhout D; Halley DJ; de Rooij FW; Wilson JH
    Hum Mutat; 1999; 13(6):476-81. PubMed ID: 10408777
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence.
    Wang ZJ; Ellis I; Zauber P; Iwama T; Marchese C; Talbot I; Xue WH; Yan ZY; Tomlinson I
    J Pathol; 1999 May; 188(1):9-13. PubMed ID: 10398133
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Increased risk of cancer in the Peutz-Jeghers syndrome.
    Giardiello FM; Welsh SB; Hamilton SR; Offerhaus GJ; Gittelsohn AM; Booker SV; Krush AJ; Yardley JH; Luk GD
    N Engl J Med; 1987 Jun; 316(24):1511-4. PubMed ID: 3587280
    [TBL] [Abstract][Full Text] [Related]  

  • 16. STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.
    Jiang CY; Esufali S; Berk T; Gallinger S; Cohen Z; Tobi M; Redston M; Bapat B
    Clin Genet; 1999 Aug; 56(2):136-41. PubMed ID: 10517250
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients.
    Yoon KA; Ku JL; Choi HS; Heo SC; Jeong SY; Park YJ; Kim NK; Kim JC; Jung PM; Park JG
    Br J Cancer; 2000 Apr; 82(8):1403-6. PubMed ID: 10780518
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.
    Gruber SB; Entius MM; Petersen GM; Laken SJ; Longo PA; Boyer R; Levin AM; Mujumdar UJ; Trent JM; Kinzler KW; Vogelstein B; Hamilton SR; Polymeropoulos MH; Offerhaus GJ; Giardiello FM
    Cancer Res; 1998 Dec; 58(23):5267-70. PubMed ID: 9850045
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Loss of cytoplasmic retention ability of mutant LKB1 found in Peutz-Jeghers syndrome patients.
    Nezu J; Oku A; Shimane M
    Biochem Biophys Res Commun; 1999 Aug; 261(3):750-5. PubMed ID: 10441497
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
    Jenne DE; Reimann H; Nezu J; Friedel W; Loff S; Jeschke R; Müller O; Back W; Zimmer M
    Nat Genet; 1998 Jan; 18(1):38-43. PubMed ID: 9425897
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.