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 *

447 related articles for article (PubMed ID: 17404884)

  • 1. Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.
    Mehenni H; Resta N; Guanti G; Mota-Vieira L; Lerner A; Peyman M; Chong KA; Aissa L; Ince A; Cosme A; Costanza MC; Rossier C; Radhakrishna U; Burt RW; Picard D
    Dig Dis Sci; 2007 Aug; 52(8):1924-33. PubMed ID: 17404884
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma.
    Olschwang S; Boisson C; Thomas G
    J Med Genet; 2001 Jun; 38(6):356-60. PubMed ID: 11389158
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Detection and analysis of common pathogenic germline mutations in Peutz-Jeghers syndrome.
    Gu GL; Zhang Z; Zhang YH; Yu PF; Dong ZW; Yang HR; Yuan Y
    World J Gastroenterol; 2021 Oct; 27(39):6631-6646. PubMed ID: 34754157
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Large deletions and splicing-site mutations in the STK11 gene in Peutz-Jeghers Chilean families.
    Orellana P; López-Köstner F; Heine C; Suazo C; Pinto E; Church J; Carvallo P; Alvarez K
    Clin Genet; 2013 Apr; 83(4):365-9. PubMed ID: 22775437
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 89(2):308-13. PubMed ID: 12865922
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Mutation analysis of related genes in hamartoma polyp tissue of Peutz-Jeghers syndrome.
    Zhang Z; Duan FX; Gu GL; Yu PF
    World J Gastroenterol; 2020 Apr; 26(16):1926-1937. PubMed ID: 32390703
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Two novel STK11 mutations in three Chinese families with Peutz-Jeghers syndrome.
    Zuo YG; Xu KJ; Su B; Ho MG; Liu YH
    Chin Med J (Engl); 2007 Jul; 120(13):1183-6. PubMed ID: 17637250
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Mutations in the human LKB1/STK11 gene.
    Launonen V
    Hum Mutat; 2005 Oct; 26(4):291-7. PubMed ID: 16110486
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.