BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 22168747)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. One novel deletion and one splicing mutation of the LKB1 gene in two Chinese patients with Peutz-Jeghers syndrome.
    Chen C; Zhang X; Wang F; Liu C; Lu H; Wan H; Wei J; Liu J
    DNA Cell Biol; 2012 Oct; 31(10):1535-40. PubMed ID: 22928647
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.
    Ausavarat S; Leoyklang P; Vejchapipat P; Chongsrisawat V; Suphapeetiporn K; Shotelersuk V
    World J Gastroenterol; 2009 Nov; 15(42):5364-7. PubMed ID: 19908348
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.