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 *

169 related articles for article (PubMed ID: 27821076)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 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. Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome.
    Yang HR; Ko JS; Seo JK
    Dig Dis Sci; 2010 Dec; 55(12):3458-65. PubMed ID: 20393878
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report.
    Tan H; Wei X; Yang P; Huang Y; Li H; Liang D; Wu L
    Fam Cancer; 2017 Jul; 16(3):417-422. PubMed ID: 28185117
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation.
    Zhao HM; Yang YJ; Duan JQ; Ouyang HJ; Liu L; Yi LC; Xiao ZH; Zheng Y; Peng L; Attard TM; Li DY; You JY
    J Pediatr Gastroenterol Nutr; 2019 Feb; 68(2):199-206. PubMed ID: 30334930
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk.
    Wang Z; Liu S; Liu S; Wang Y; Chen J; Wu B
    BMC Med Genet; 2018 May; 19(1):66. PubMed ID: 29720104
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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 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]  

  • 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. 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]  

  • 19. First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
    McKay V; Cairns D; Gokhale D; Mountford R; Greenhalgh L
    Fam Cancer; 2016 Jan; 15(1):57-61. PubMed ID: 26386697
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 9.