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 *

155 related articles for article (PubMed ID: 37377590)

  • 21. 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]  

  • 22. 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]  

  • 23. Exome sequencing revealed novel germline mutations in Chinese Peutz-Jeghers syndrome patients.
    Wang HH; Xie NN; Li QY; Hu YQ; Ren JL; Guleng B
    Dig Dis Sci; 2014 Jan; 59(1):64-71. PubMed ID: 24154639
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma.
    Olschwang S; Boisson C; Thomas G
    J Med Genet; 2001 Jun; 38(6):356-60. PubMed ID: 11389158
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Extremely young case of small bowel intussusception due to Peutz-Jeghers syndrome with nonsense mutation of STK11.
    Sado T; Nakayama Y; Kato S; Homma H; Kusakari M; Hidaka N; Gomi S; Takamizawa S; Kosho T; Saito S; Sugano K
    Clin J Gastroenterol; 2019 Oct; 12(5):429-433. PubMed ID: 30888642
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.
    Mehenni H; Resta N; Guanti G; Mota-Vieira L; Lerner A; Peyman M; Chong KA; Aissa L; Ince A; Cosme A; Costanza MC; Rossier C; Radhakrishna U; Burt RW; Picard D
    Dig Dis Sci; 2007 Aug; 52(8):1924-33. PubMed ID: 17404884
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
    Hearle N; Lucassen A; Wang R; Lim W; Ross F; Wheeler R; Moore I; Shipley J; Houlston R
    Genes Chromosomes Cancer; 2004 Oct; 41(2):163-9. PubMed ID: 15287029
    [TBL] [Abstract][Full Text] [Related]  

  • 31. De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome.
    Hernan I; Roig I; Martin B; Gamundi MJ; Martinez-Gimeno M; Carballo M
    Clin Genet; 2004 Jul; 66(1):58-62. PubMed ID: 15200509
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome.
    Le Meur N; Martin C; Saugier-Veber P; Joly G; Lemoine F; Moirot H; Rossi A; Bachy B; Cabot A; Joly P; Frébourg T
    Eur J Hum Genet; 2004 May; 12(5):415-8. PubMed ID: 14970844
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Must Peutz-Jeghers syndrome patients have the
    Duan FX; Gu GL; Yang HR; Yu PF; Zhang Z
    World J Clin Cases; 2018 Aug; 6(8):224-232. PubMed ID: 30148152
    [TBL] [Abstract][Full Text] [Related]  

  • 34. STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.
    Jiang CY; Esufali S; Berk T; Gallinger S; Cohen Z; Tobi M; Redston M; Bapat B
    Clin Genet; 1999 Aug; 56(2):136-41. PubMed ID: 10517250
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Mutations in STK11 gene in Czech Peutz-Jeghers patients.
    Vasovcák P; Puchmajerová A; Roubalík J; Krepelová A
    BMC Med Genet; 2009 Jul; 10():69. PubMed ID: 19615099
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Peutz-Jeghers syndrome].
    Miyaki M
    Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.