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 *

176 related articles for article (PubMed ID: 30444588)

  • 1. [Pilot clinical and genetic study of Russian patients with Peutz-Jeghers syndrome].
    Shelygin YA; Pospekhova NI; Shubin VP; Kashnikov VN; Frolov SA; Kuzminov AM; Mainovskaya OA; Sachkov IY; Tsukanov AS
    Vopr Onkol; 2016; 62(1):112-16. PubMed ID: 30444588
    [TBL] [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. 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]  

  • 4. Disease pattern in Danish patients with Peutz-Jeghers syndrome.
    Jelsig AM; Qvist N; Sunde L; Brusgaard K; Hansen T; Wikman FP; Nielsen CB; Nielsen IK; Gerdes AM; Bojesen A; Ousager LB
    Int J Colorectal Dis; 2016 May; 31(5):997-1004. PubMed ID: 26979979
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Rare hereditary syndromes associated with polyposis and the development of malignant tumors].
    Kazubskaya TP; Kozlova VM; Filippova MG; Тrofimov EI; Belev NF; Sokolova IN; Tamrazov RI; Pavlovskaya AI; Kondratyeva TT
    Arkh Patol; 2016; 78(2):10-18. PubMed ID: 27070770
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
    Hemminki A; Markie D; Tomlinson I; Avizienyte E; Roth S; Loukola A; Bignell G; Warren W; Aminoff M; Höglund P; Järvinen H; Kristo P; Pelin K; Ridanpää M; Salovaara R; Toro T; Bodmer W; Olschwang S; Olsen AS; Stratton MR; de la Chapelle A; Aaltonen LA
    Nature; 1998 Jan; 391(6663):184-7. PubMed ID: 9428765
    [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. A Peutz-Jeghers syndrome family associated with sinonasal adenocarcinoma: 28 years follow up report.
    Chiang JM; Chen TC
    Fam Cancer; 2017 Oct; 16(4):555-560. PubMed ID: 28391433
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic and epigenetic profiling of a solitary Peutz-Jeghers colon polyp.
    Linhart H; Bormann F; Hutter B; Brors B; Lyko F
    Cold Spring Harb Mol Case Stud; 2017 May; 3(3):a001610. PubMed ID: 28487883
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. [The course and clinical manifestations of Peutz-Jeghers syndrome in the Russian population].
    Savelyeva ТA; Ponomarenko АA; Shelygin YA; Kuzminov АM; Vyshegorodtsev DV; Loginova АN; Pikunov DY; Goncharova ЕP; Likutov АA; Mainovskaya ОA; Tsukanov АS
    Ter Arkh; 2023 Mar; 95(2):145-151. PubMed ID: 37167130
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular insights into Peutz-Jeghers syndrome: two probands with a germline mutation of LKB1.
    Hosogi H; Nagayama S; Kawamura J; Koshiba Y; Nomura A; Itami A; Okabe H; Satoh S; Watanabe G; Sakai Y
    J Gastroenterol; 2008; 43(6):492-7. PubMed ID: 18600394
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genetic analysis of Peutz-Jeghers syndrome patients in Taiwan.
    Weng MT; Ni YH; Su YN; Wong JM; Wei SC
    J Formos Med Assoc; 2010 May; 109(5):354-61. PubMed ID: 20497868
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Hamartomatous polyps - a clinical and molecular genetic study.
    Jelsig AM
    Dan Med J; 2016 Aug; 63(8):. PubMed ID: 27477802
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. Peutz-Jeghers syndrome polyps are polyclonal with expanded progenitor cell compartment.
    de Leng WW; Jansen M; Keller JJ; de Gijsel M; Milne AN; Morsink FH; Weterman MA; Iacobuzio-Donahue CA; Clevers HC; Giardiello FM; Offerhaus GJ
    Gut; 2007 Oct; 56(10):1475-6. PubMed ID: 17872577
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.