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 *

206 related articles for article (PubMed ID: 29141581)

  • 1. 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]  

  • 2. A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.
    Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Ning SB; Sun SH
    Dig Dis Sci; 2017 Nov; 62(11):3014-3020. PubMed ID: 28986664
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. [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]  

  • 9. [Mutation analysis of STK11 gene in a Chinese family with Peutz-Jeghers syndrome].
    Zhao X; Huang Y; Yang B; Zhao Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):294-7. PubMed ID: 24928005
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Analysis of STK11 gene variant in five Chinese patients with Peutz-Jeghers syndrome.
    Zheng B; Pan J; Wang Y; Li M; Lian M; Zheng Y; Jin Y
    Dig Dis Sci; 2013 Oct; 58(10):2868-72. PubMed ID: 23892522
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a novel de novo STK11 mutation in a Chinese child with Peutz-Jeghers syndrome.
    Liu WL; Li F; He ZX; Jiang HY; Ai R; Zhu XP; Chen XX; Ma HW
    J Int Med Res; 2011; 39(5):2033-8. PubMed ID: 22118009
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic variation at a splicing branch point in intron 7 of STK11: a rare variant decreasing its expression in a Chinese family with Peutz-Jeghers syndrome.
    Wang X; Li Y; Zhang J; Liu C; Deng A; Li J
    World J Surg Oncol; 2024 Jul; 22(1):202. PubMed ID: 39080663
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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. A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report.
    Chen JH; Zheng JJ; Guo Q; Liu C; Luo B; Tang SB; Cheng JD; Huang EW
    BMC Med Genet; 2017 Feb; 18(1):19. PubMed ID: 28231849
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.
    Zhao ZY; Jiang YL; Li BR; Li J; Jin XW; Yu ED; Ning SB
    BMC Surg; 2018 Apr; 18(1):24. PubMed ID: 29685139
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.