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.
191 related articles for article (PubMed ID: 23718779)
1. High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome. Borun P; Bartkowiak A; Banasiewicz T; Nedoszytko B; Nowakowska D; Teisseyre M; Limon J; Lubinski J; Kubaszewski L; Walkowiak J; Czkwianianc E; Siolek M; Kedzia A; Krokowicz P; Cichy W; Plawski A BMC Med Genet; 2013 May; 14():58. PubMed ID: 23718779 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome. Borun P; De Rosa M; Nedoszytko B; Walkowiak J; Plawski A Fam Cancer; 2015 Sep; 14(3):455-61. PubMed ID: 25841653 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome. Yoo JH; Yoo JH; Choi YJ; Kang JG; Sun YK; Ki CS; Lee KA; Choi JR BMC Med Genet; 2008 May; 9():44. PubMed ID: 18495044 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. [Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome]. Mao X; Zhang Y; Wang H; Mao G; Ning S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):186-90. PubMed ID: 27060312 [TBL] [Abstract][Full Text] [Related]
11. 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]
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. 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]
14. [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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. Hearle NC; Rudd MF; Lim W; Murday V; Lim AG; Phillips RK; Lee PW; O'donohue J; Morrison PJ; Norman A; Hodgson SV; Lucassen A; Houlston RS J Med Genet; 2006 Apr; 43(4):e15. PubMed ID: 16582077 [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]