BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 28303455)

  • 1. Duodenal cancer in a young patient with Peuts-Jeghers syndrome harboring an entire deletion of the STK11 gene.
    Teramae S; Okamoto K; Tanaka K; Matsumoto R; Kitamura S; Kimura T; Sogabe M; Miyamoto H; Muguruma N; Bando Y; Shimada M; Takayama T
    Clin J Gastroenterol; 2017 Jun; 10(3):232-239. PubMed ID: 28303455
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duodenal cancer in a patient with Peutz-Jeghers syndrome: molecular analysis.
    Nakamura T; Suzuki S; Yokoi Y; Kashiwabara H; Maruyama K; Baba S; Nakagawa H; Nakamura S
    J Gastroenterol; 2002; 37(5):376-80. PubMed ID: 12051537
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
    Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
    Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers.
    Su GH; Hruban RH; Bansal RK; Bova GS; Tang DJ; Shekher MC; Westerman AM; Entius MM; Goggins M; Yeo CJ; Kern SE
    Am J Pathol; 1999 Jun; 154(6):1835-40. PubMed ID: 10362809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.
    Miyaki M; Iijima T; Hosono K; Ishii R; Yasuno M; Mori T; Toi M; Hishima T; Shitara N; Tamura K; Utsunomiya J; Kobayashi N; Kuroki T; Iwama T
    Cancer Res; 2000 Nov; 60(22):6311-3. PubMed ID: 11103790
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome.
    Entius MM; Keller JJ; Westerman AM; van Rees BP; van Velthuysen ML; de Goeij AF; Wilson JH; Giardiello FM; Offerhaus GJ
    J Clin Pathol; 2001 Feb; 54(2):126-31. PubMed ID: 11215281
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Solitary Peutz-Jeghers Type Polyp of Jejunum with Gastric Fundic and Antral Gland Lining Mucosa: A Case Report and Review of Literature.
    Liu BL; Zhou H; Risech M; Ky A; Houldsworth J; Ward SC
    Int J Surg Pathol; 2022 Aug; 30(5):539-542. PubMed ID: 34955063
    [TBL] [Abstract][Full Text] [Related]  

  • 13. STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
    Wang Z; Wu B; Mosig RA; Chen Y; Ye F; Zhang Y; Gong W; Gong L; Huang F; Wang X; Nie B; Zheng H; Cui M; Wang Y; Wang J; Chen C; Polydorides AD; Zhang DY; Martignetti JA; Jiang B
    Hum Mutat; 2014 Jul; 35(7):851-8. PubMed ID: 24652667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A solitary Peutz-Jeghers-type hamartomatous polyp in the duodenum. A case report including results of mutation analysis.
    Kitaoka F; Shiogama T; Mizutani A; Tsurunaga Y; Fukui H; Higami Y; Shimokawa I; Taguchi T; Kanematsu T
    Digestion; 2004; 69(2):79-82. PubMed ID: 15031625
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Clinical features, endoscopic polypectomy and STK11 gene mutation in a nine-month-old Peutz-Jeghers syndrome Chinese infant.
    Huang ZH; Song Z; Zhang P; Wu J; Huang Y
    World J Gastroenterol; 2016 Mar; 22(11):3261-7. PubMed ID: 27004004
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Primary gastric adenocarcinoma in a patient with Peutz-Jeghers syndrome.
    Ortega Lobete O; Díaz Ruiz R; Pérez Carazo L
    Rev Esp Enferm Dig; 2021 Jun; 113(6):474-475. PubMed ID: 33244976
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.