BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 26289244)

  • 1. [Peutz-Jeghers Syndrome with Adenomatous Change in a Fifteen-month-old Boy].
    Lee KS; Lee SH; Myong NH
    Korean J Gastroenterol; 2015 Aug; 66(2):106-10. PubMed ID: 26289244
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.
    Miyaki M; Iijima T; Hosono K; Ishii R; Yasuno M; Mori T; Toi M; Hishima T; Shitara N; Tamura K; Utsunomiya J; Kobayashi N; Kuroki T; Iwama T
    Cancer Res; 2000 Nov; 60(22):6311-3. PubMed ID: 11103790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Peutz-Jeghers syndrome: risks of a hereditary condition.
    Westerman AM; Wilson JH
    Scand J Gastroenterol Suppl; 1999; 230():64-70. PubMed ID: 10499464
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 15121768
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity.
    de Leng WW; Westerman AM; Weterman MA; Jansen M; van Dekken H; Giardiello FM; de Rooij FW; Paul Wilson JH; Offerhaus GJ; Keller JJ
    J Clin Pathol; 2007 Apr; 60(4):392-6. PubMed ID: 16775120
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Malignancy and overdiagnosis of malignancy in Peutz Jeghers polyposis.
    Zurac S; Micu G; Bastian A; Grămadă E; Lavric L; Andrei R; Stăniceanu F; Voiosu R; Croitoru A
    Rom J Intern Med; 2008; 46(2):179-84. PubMed ID: 19284092
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposis.
    Jansen M; de Leng WW; Baas AF; Myoshi H; Mathus-Vliegen L; Taketo MM; Clevers H; Giardiello FM; Offerhaus GJ
    Gut; 2006 Jan; 55(1):1-5. PubMed ID: 16344569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome.
    Entius MM; Keller JJ; Westerman AM; van Rees BP; van Velthuysen ML; de Goeij AF; Wilson JH; Giardiello FM; Offerhaus GJ
    J Clin Pathol; 2001 Feb; 54(2):126-31. PubMed ID: 11215281
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
    Hearle N; Lucassen A; Wang R; Lim W; Ross F; Wheeler R; Moore I; Shipley J; Houlston R
    Genes Chromosomes Cancer; 2004 Oct; 41(2):163-9. PubMed ID: 15287029
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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; 7():73. PubMed ID: 17010210
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Peutz-Jeghers syndrome: case reports and update on diagnosis and treatment.
    Dong K; Li B
    Chin J Dig Dis; 2004; 5(4):160-4. PubMed ID: 15612885
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome.
    Yoo JH; Yoo JH; Choi YJ; Kang JG; Sun YK; Ki CS; Lee KA; Choi JR
    BMC Med Genet; 2008 May; 9():44. PubMed ID: 18495044
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical analysis of Peutz-Jeghers syndrome:a report of 6 cases].
    Dong K; Li B; Li BH; Guan QL; Huo YZ
    Zhonghua Wei Chang Wai Ke Za Zhi; 2005 Jul; 8(4):336-8. PubMed ID: 16167257
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.