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 *

163 related articles for article (PubMed ID: 24604241)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. [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]  

  • 6. [Analysis of STK11 gene variants among 64 patients with Peutz-Jeghers syndrome].
    Li M; Sun T; Jiang Y; Li J; Ning S; Zhou P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep; 36(9):862-865. PubMed ID: 31515776
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 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. 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]  

  • 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. 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. A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.
    Zheng B; Wang C; Jia Z; Liu Z; Li M; Jin Y; Pan J
    J Pediatr Gastroenterol Nutr; 2017 Apr; 64(4):559-564. PubMed ID: 27467201
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome.
    Jiang YL; Zhao ZY; Li BR; Yang F; Li J; Jin XW; Wang H; Yu ED; Sun SH; Ning SB
    BMC Med Genet; 2018 Aug; 19(1):141. PubMed ID: 30092773
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients.
    Jiang YL; Zhao ZY; Li BR; Wang H; Yu ED; Ning SB
    Cancer Genet; 2019 Jan; 230():47-57. PubMed ID: 30528796
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.