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22. Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer. Bignell GR; Barfoot R; Seal S; Collins N; Warren W; Stratton MR Cancer Res; 1998 Apr; 58(7):1384-6. PubMed ID: 9537235 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2. Buchet-Poyau K; Mehenni H; Radhakrishna U; Antonarakis SE Cytogenet Genome Res; 2002; 97(3-4):171-8. PubMed ID: 12438709 [TBL] [Abstract][Full Text] [Related]
25. [Germline LKB1 gene mutation screening in 4 Chinese Peutz-Jeghers syndrome pedigrees]. Wang Z; Yan Z; Bi G; Xu W; Huang T Zhonghua Wai Ke Za Zhi; 2000 Feb; 38(2):104-5. PubMed ID: 11832000 [TBL] [Abstract][Full Text] [Related]
26. Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRAD. Baas AF; Boudeau J; Sapkota GP; Smit L; Medema R; Morrice NA; Alessi DR; Clevers HC EMBO J; 2003 Jun; 22(12):3062-72. PubMed ID: 12805220 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Regulation of the Wnt signalling component PAR1A by the Peutz-Jeghers syndrome kinase LKB1. Spicer J; Rayter S; Young N; Elliott R; Ashworth A; Smith D Oncogene; 2003 Jul; 22(30):4752-6. PubMed ID: 12879020 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome. Kortschak RD; Reimann H; Zimmer M; Eyre HJ; Saint R; Jenne DE Genomics; 1998 Jul; 51(2):288-92. PubMed ID: 9722953 [TBL] [Abstract][Full Text] [Related]
34. Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Hearle N; Schumacher V; Menko FH; Olschwang S; Boardman LA; Gille JJ; Keller JJ; Westerman AM; Scott RJ; Lim W; Trimbath JD; Giardiello FM; Gruber SB; Offerhaus GJ; de Rooij FW; Wilson JH; Hansmann A; Möslein G; Royer-Pokora B; Vogel T; Phillips RK; Spigelman AD; Houlston RS Clin Cancer Res; 2006 May; 12(10):3209-15. PubMed ID: 16707622 [TBL] [Abstract][Full Text] [Related]
35. Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. Ylikorkala A; Avizienyte E; Tomlinson IP; Tiainen M; Roth S; Loukola A; Hemminki A; Johansson M; Sistonen P; Markie D; Neale K; Phillips R; Zauber P; Twama T; Sampson J; Järvinen H; Mäkelä TP; Aaltonen LA Hum Mol Genet; 1999 Jan; 8(1):45-51. PubMed ID: 9887330 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Effects of Peutz-Jeghers syndrome (PJS) causing missense mutations L67P, L182P, G242V and R297S on the structural dynamics of LKB1 (Liver kinase B1) protein. Rungsung I; Ramaswamy A J Biomol Struct Dyn; 2019 Feb; 37(3):796-810. PubMed ID: 29447078 [TBL] [Abstract][Full Text] [Related]
38. Stability of the Peutz-Jeghers syndrome kinase LKB1 requires its binding to the molecular chaperones Hsp90/Cdc37. Nony P; Gaude H; Rossel M; Fournier L; Rouault JP; Billaud M Oncogene; 2003 Dec; 22(57):9165-75. PubMed ID: 14668798 [TBL] [Abstract][Full Text] [Related]
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40. 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] [Previous] [Next] [New Search]