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 *

198 related articles for article (PubMed ID: 28869103)

  • 1. 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]  

  • 2. 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]  

  • 3. Peutz-Jeghers syndrome without
    Jiang LX; Chen YR; Xu ZX; Zhang YH; Zhang Z; Yu PF; Dong ZW; Yang HR; Gu GL
    World J Gastroenterol; 2023 Jun; 29(21):3302-3317. PubMed ID: 37377590
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.
    Huang Z; Miao S; Wang L; Zhang P; Wu B; Wu J; Huang Y
    BMC Gastroenterol; 2015 Nov; 15():166. PubMed ID: 26607058
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.
    Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Ning SB; Sun SH
    BMC Med Genet; 2017 Nov; 18(1):130. PubMed ID: 29141581
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome.
    Aslan PG; Çağlayan AO; Bora E; Koç A; Yücel H; Ülgenalp A; Öztürk Y; Şeker G; Akarsu M
    Turk J Gastroenterol; 2024 Mar; 35(5):374-384. PubMed ID: 39115133
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.
    Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Sun SH; Ning SB
    Medicine (Baltimore); 2017 Dec; 96(49):e8591. PubMed ID: 29245219
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Mutation analysis of STK11 gene coding region for 20 Chinese patients with Peutz-Jeghers syndrome].
    Zhao X; Li Y; Ling Y; Chen H; Zhang B; Xia T; Zhou P
    Nan Fang Yi Ke Da Xue Xue Bao; 2012 Apr; 32(4):511-4. PubMed ID: 22543132
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome.
    Wu BD; Wang YJ; Fan LL; Huang H; Zhou P; Yang M; Shi XL
    Biomed Res Int; 2020; 2020():9159315. PubMed ID: 32462036
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.
    Tan H; Mei L; Huang Y; Yang P; Li H; Peng Y; Chen C; Wei X; Pan Q; Liang D; Wu L
    BMC Med Genet; 2016 Nov; 17(1):77. PubMed ID: 27821076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A novel mutation in STK11 gene is associated with Peutz-Jeghers syndrome in Chinese patients.
    Wang Z; Chen Y; Wu B; Zheng H; He J; Jiang B
    BMC Med Genet; 2011 Dec; 12():161. PubMed ID: 22168747
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Novel and recurrent mutations of STK11 gene in six Chinese cases with Peutz-Jeghers syndrome.
    Dai L; Fu L; Liu D; Zhang K; Wu Y; Meng H; Zhang B; Guan X; Guo H; Bai Y
    Dig Dis Sci; 2014 Aug; 59(8):1856-61. PubMed ID: 24604241
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.