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.
165 related articles for article (PubMed ID: 14726968)
1. A new mutation of LKB1 gene in a Japanese patient with Peutz-Jeghers syndrome. Tate G; Suzuki T; Mitsuya T Acta Med Okayama; 2003 Dec; 57(6):305-8. PubMed ID: 14726968 [TBL] [Abstract][Full Text] [Related]
2. 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]
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. 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. [Clinical characteristics and mutation analysis of the LKB1 gene in a Peutz-Jeghers syndrome pedigree]. Pan J; Li M; Jin Y; Zhang XM; Zhu M; Chen SQ Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):145-9. PubMed ID: 23527983 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. Wang ZJ; Churchman M; Avizienyte E; McKeown C; Davies S; Evans DG; Ferguson A; Ellis I; Xu WH; Yan ZY; Aaltonen LA; Tomlinson IP J Med Genet; 1999 May; 36(5):365-8. PubMed ID: 10353780 [TBL] [Abstract][Full Text] [Related]
8. Molecular insights into Peutz-Jeghers syndrome: two probands with a germline mutation of LKB1. Hosogi H; Nagayama S; Kawamura J; Koshiba Y; Nomura A; Itami A; Okabe H; Satoh S; Watanabe G; Sakai Y J Gastroenterol; 2008; 43(6):492-7. PubMed ID: 18600394 [TBL] [Abstract][Full Text] [Related]
9. Ganglioglioma arising in a Peutz-Jeghers patient: a case report with molecular implications. Resta N; Lauriola L; Puca A; Susca FC; Albanese A; Sabatino G; Di Giacomo MC; Gessi M; Guanti G Acta Neuropathol; 2006 Jul; 112(1):106-11. PubMed ID: 16733653 [TBL] [Abstract][Full Text] [Related]
10. Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families. Westerman AM; Entius MM; Boor PP; Koole R; de Baar E; Offerhaus GJ; Lubinski J; Lindhout D; Halley DJ; de Rooij FW; Wilson JH Hum Mutat; 1999; 13(6):476-81. PubMed ID: 10408777 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. A novel germline mutation of the LKB1 gene in a patient with Peutz-Jeghers syndrome with early-onset gastric cancer. Takahashi M; Sakayori M; Takahashi S; Kato T; Kaji M; Kawahara M; Suzuki T; Kato S; Kato S; Shibata H; Murakawa Y; Yoshioka T; Ishioka C J Gastroenterol; 2004 Dec; 39(12):1210-4. PubMed ID: 15622488 [TBL] [Abstract][Full Text] [Related]
13. 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]
15. 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]
16. A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity. Liu L; Du X; Nie J Clin Res Hepatol Gastroenterol; 2011 Mar; 35(3):221-6. PubMed ID: 21411391 [TBL] [Abstract][Full Text] [Related]
17. Mutation analysis of related genes in hamartoma polyp tissue of Peutz-Jeghers syndrome. Zhang Z; Duan FX; Gu GL; Yu PF World J Gastroenterol; 2020 Apr; 26(16):1926-1937. PubMed ID: 32390703 [TBL] [Abstract][Full Text] [Related]
19. Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity. Mehenni H; Gehrig C; Nezu J; Oku A; Shimane M; Rossier C; Guex N; Blouin JL; Scott HS; Antonarakis SE Am J Hum Genet; 1998 Dec; 63(6):1641-50. PubMed ID: 9837816 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]