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.
330 related articles for article (PubMed ID: 9934767)
1. Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11. Trojan J; Brieger A; Raedle J; Roth WK; Zeuzem S Am J Gastroenterol; 1999 Jan; 94(1):257-61. PubMed ID: 9934767 [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. Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online. Kruse R; Uhlhaas S; Lamberti C; Keller KM; Jackisch C; Steinhard J; Knöpfle G; Loff S; Back W; Stolte M; Jungck M; Propping P; Friedl W; Jenne DE Hum Mutat; 1999; 13(3):257-8. PubMed ID: 10090485 [TBL] [Abstract][Full Text] [Related]
4. Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4). Abed AA; Günther K; Kraus C; Hohenberger W; Ballhausen WG Hum Mutat; 2001 Nov; 18(5):397-410. PubMed ID: 11668633 [TBL] [Abstract][Full Text] [Related]
5. STK11/LKB1 germline mutations in the first Peutz-Jeghers syndrome patients identified in Slovakia. Bartosova Z; Zavodna K; Krivulcik T; Usak J; Mlkva I; Kruzliak T; Hromec J; Usakova V; Kopecka I; Veres P; Bartosova Z; Bujalkova M Neoplasma; 2007; 54(2):101-7. PubMed ID: 17319781 [TBL] [Abstract][Full Text] [Related]
6. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Jenne DE; Reimann H; Nezu J; Friedel W; Loff S; Jeschke R; Müller O; Back W; Zimmer M Nat Genet; 1998 Jan; 18(1):38-43. PubMed ID: 9425897 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. A novel STK11 germline mutation in two siblings with Peutz-Jeghers syndrome complicated by primary gastric cancer. Shinmura K; Goto M; Tao H; Shimizu S; Otsuki Y; Kobayashi H; Ushida S; Suzuki K; Tsuneyoshi T; Sugimura H Clin Genet; 2005 Jan; 67(1):81-6. PubMed ID: 15617552 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients. Resta N; Stella A; Susca FC; Di Giacomo M; Forleo G; Miccolis I; Rossini FP; Genuardi M; Piepoli A; Grammatico P; Guanti G Hum Mutat; 2002 Jul; 20(1):78-9. PubMed ID: 12112668 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Different phenotypes including gynecological cancer in three female patients with Peutz-Jeghers syndrome and mutations in the STK11 gene. Heinritz W; Strenge S; Kujat A; Hockel M; Froster UG Onkologie; 2008 Nov; 31(11):625-8. PubMed ID: 19145097 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]