BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 15863673)

  • 1. STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.
    Schumacher V; Vogel T; Leube B; Driemel C; Goecke T; Möslein G; Royer-Pokora B
    J Med Genet; 2005 May; 42(5):428-35. PubMed ID: 15863673
    [No Abstract]   [Full Text] [Related]  

  • 2. Genetic screening for Peutz-Jeghers syndrome.
    Ballhausen WG; Günther K
    Expert Rev Mol Diagn; 2003 Jul; 3(4):471-9. PubMed ID: 12877386
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Frequency and spectrum of cancers in the 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; de Rooij FW; Wilson JH; Hansmann A; Möslein G; Royer-Pokora B; Vogel T; Phillips RK; Spigelman AD; Houlston RS
    Clin Cancer Res; 2006 May; 12(10):3209-15. PubMed ID: 16707622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel STK11 germline mutation in two siblings with Peutz-Jeghers syndrome complicated by primary gastric cancer.
    Shinmura K; Goto M; Tao H; Shimizu S; Otsuki Y; Kobayashi H; Ushida S; Suzuki K; Tsuneyoshi T; Sugimura H
    Clin Genet; 2005 Jan; 67(1):81-6. PubMed ID: 15617552
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

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

  • 7. De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome.
    Hernan I; Roig I; Martin B; Gamundi MJ; Martinez-Gimeno M; Carballo M
    Clin Genet; 2004 Jul; 66(1):58-62. PubMed ID: 15200509
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
    Hearle NC; Rudd MF; Lim W; Murday V; Lim AG; Phillips RK; Lee PW; O'donohue J; Morrison PJ; Norman A; Hodgson SV; Lucassen A; Houlston RS
    J Med Genet; 2006 Apr; 43(4):e15. PubMed ID: 16582077
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
    Wang Z; Wu B; Mosig RA; Chen Y; Ye F; Zhang Y; Gong W; Gong L; Huang F; Wang X; Nie B; Zheng H; Cui M; Wang Y; Wang J; Chen C; Polydorides AD; Zhang DY; Martignetti JA; Jiang B
    Hum Mutat; 2014 Jul; 35(7):851-8. PubMed ID: 24652667
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mutated serine-threonine kinase gene (STK11) is the cause of Peutz-Jeghers syndrome].
    Trojan J; Raedle J; Zeuzem S
    Z Gastroenterol; 1998 Sep; 36(9):871-3. PubMed ID: 9795419
    [No Abstract]   [Full Text] [Related]  

  • 12. 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. PubMed ID: 16407375
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. STK11/LKB1 germline mutations in the first Peutz-Jeghers syndrome patients identified in Slovakia.
    Bartosova Z; Zavodna K; Krivulcik T; Usak J; Mlkva I; Kruzliak T; Hromec J; Usakova V; Kopecka I; Veres P; Bartosova Z; Bujalkova M
    Neoplasma; 2007; 54(2):101-7. PubMed ID: 17319781
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Different phenotypes including gynecological cancer in three female patients with Peutz-Jeghers syndrome and mutations in the STK11 gene.
    Heinritz W; Strenge S; Kujat A; Hockel M; Froster UG
    Onkologie; 2008 Nov; 31(11):625-8. PubMed ID: 19145097
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel germline mutation of the LKB1 gene in a patient with Peutz-Jeghers syndrome with early-onset gastric cancer.
    Takahashi M; Sakayori M; Takahashi S; Kato T; Kaji M; Kawahara M; Suzuki T; Kato S; Kato S; Shibata H; Murakawa Y; Yoshioka T; Ishioka C
    J Gastroenterol; 2004 Dec; 39(12):1210-4. PubMed ID: 15622488
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
    Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
    Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients.
    Resta N; Stella A; Susca FC; Di Giacomo M; Forleo G; Miccolis I; Rossini FP; Genuardi M; Piepoli A; Grammatico P; Guanti G
    Hum Mutat; 2002 Jul; 20(1):78-9. PubMed ID: 12112668
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
    Chow E; Meldrum CJ; Crooks R; Macrae F; Spigelman AD; Scott RJ
    Clin Genet; 2006 Nov; 70(5):409-14. PubMed ID: 17026623
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome.
    Le Meur N; Martin C; Saugier-Veber P; Joly G; Lemoine F; Moirot H; Rossi A; Bachy B; Cabot A; Joly P; Frébourg T
    Eur J Hum Genet; 2004 May; 12(5):415-8. PubMed ID: 14970844
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.