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22. 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]
23. 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]
24. 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]
25. 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]
26. LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes. Mehenni H; Lin-Marq N; Buchet-Poyau K; Reymond A; Collart MA; Picard D; Antonarakis SE Hum Mol Genet; 2005 Aug; 14(15):2209-19. PubMed ID: 15987703 [TBL] [Abstract][Full Text] [Related]
27. [Peutz-Jeghers syndrome: case report and update on diagnosis and treatment]. Capasso L; Lombari P; Scarano MI; Izzo P; D'Ambrosio R; Iannucci A; Formisano V; Lombari C Minerva Chir; 2001 Dec; 56(6):643-7. PubMed ID: 11721206 [TBL] [Abstract][Full Text] [Related]
28. Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome. Gruber SB; Entius MM; Petersen GM; Laken SJ; Longo PA; Boyer R; Levin AM; Mujumdar UJ; Trent JM; Kinzler KW; Vogelstein B; Hamilton SR; Polymeropoulos MH; Offerhaus GJ; Giardiello FM Cancer Res; 1998 Dec; 58(23):5267-70. PubMed ID: 9850045 [TBL] [Abstract][Full Text] [Related]
29. Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity. de Leng WW; Westerman AM; Weterman MA; Jansen M; van Dekken H; Giardiello FM; de Rooij FW; Paul Wilson JH; Offerhaus GJ; Keller JJ J Clin Pathol; 2007 Apr; 60(4):392-6. PubMed ID: 16775120 [TBL] [Abstract][Full Text] [Related]
30. Germline mutation of the LKB1/STK11 gene with loss of the normal allele in an aggressive breast cancer of Peutz-Jeghers syndrome. Nakanishi C; Yamaguchi T; Iijima T; Saji S; Toi M; Mori T; Miyaki M Oncology; 2004; 67(5-6):476-9. PubMed ID: 15714005 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome. Connolly DC; Katabuchi H; Cliby WA; Cho KR Am J Pathol; 2000 Jan; 156(1):339-45. PubMed ID: 10623683 [TBL] [Abstract][Full Text] [Related]
33. Loss of cytoplasmic retention ability of mutant LKB1 found in Peutz-Jeghers syndrome patients. Nezu J; Oku A; Shimane M Biochem Biophys Res Commun; 1999 Aug; 261(3):750-5. PubMed ID: 10441497 [TBL] [Abstract][Full Text] [Related]
34. Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome. Hearle NC; Tomlinson I; Lim W; Murday V; Swarbrick E; Lim G; Phillips R; Lee P; O'Donohue J; Trembath RC; Morrison PJ; Norman A; Taylor R; Hodgson S; Lucassen A; Houlston RS BMC Genomics; 2005 Mar; 6():38. PubMed ID: 15774015 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Lack of STK11 gene expression in homozygous twins with Peutz-Jeghers syndrome. Tseng CJ; Chen SF; Liou SI; Lu SC; Chen JM; Sun CF; Chang SD; Cheng PJ; Liou JD; Chu DC Ann Clin Lab Sci; 2004; 34(2):154-8. PubMed ID: 15228227 [TBL] [Abstract][Full Text] [Related]
38. 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]
39. Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients. Boudeau J; Kieloch A; Alessi DR; Stella A; Guanti G; Resta N Hum Mutat; 2003 Feb; 21(2):172. PubMed ID: 12552571 [TBL] [Abstract][Full Text] [Related]
40. Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours. Wang ZJ; Churchman M; Campbell IG; Xu WH; Yan ZY; McCluggage WG; Foulkes WD; Tomlinson IP Br J Cancer; 1999 Apr; 80(1-2):70-2. PubMed ID: 10389980 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]