These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

396 related articles for article (PubMed ID: 24652667)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
    McKay V; Cairns D; Gokhale D; Mountford R; Greenhalgh L
    Fam Cancer; 2016 Jan; 15(1):57-61. PubMed ID: 26386697
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.
    Borun P; De Rosa M; Nedoszytko B; Walkowiak J; Plawski A
    Fam Cancer; 2015 Sep; 14(3):455-61. PubMed ID: 25841653
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical manifestations and STK11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome.
    Chiang JM; Chen TC
    Asian J Surg; 2018 Sep; 41(5):480-485. PubMed ID: 28869103
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4).
    Abed AA; Günther K; Kraus C; Hohenberger W; Ballhausen WG
    Hum Mutat; 2001 Nov; 18(5):397-410. PubMed ID: 11668633
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.
    Zheng B; Wang C; Jia Z; Liu Z; Li M; Jin Y; Pan J
    J Pediatr Gastroenterol Nutr; 2017 Apr; 64(4):559-564. PubMed ID: 27467201
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz-Jeghers syndrome.
    Lipsa A; Kowtal P; Sarin R
    Hum Mol Genet; 2019 Jun; 28(11):1885-1893. PubMed ID: 30689838
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome.
    Yang HR; Ko JS; Seo JK
    Dig Dis Sci; 2010 Dec; 55(12):3458-65. PubMed ID: 20393878
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A De Novo mutation of STK11 gene in a Chinese patient with Peutz-Jeghers syndrome.
    Gao Y; Zhang FM; Huang S; Wang X; Zhang P; Huang XD; Ji GZ; Fan ZN
    Dig Dis Sci; 2010 Apr; 55(4):1032-6. PubMed ID: 19507030
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. 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]  

  • 40. [Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome].
    Mao X; Zhang Y; Wang H; Mao G; Ning S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):186-90. PubMed ID: 27060312
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.