234 related articles for article (PubMed ID: 10441497)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma.
Guldberg P; thor Straten P; Ahrenkiel V; Seremet T; Kirkin AF; Zeuthen J
Oncogene; 1999 Mar; 18(9):1777-80. PubMed ID: 10208439
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. LKB1, a novel serine/threonine protein kinase and potential tumour suppressor, is phosphorylated by cAMP-dependent protein kinase (PKA) and prenylated in vivo.
Collins SP; Reoma JL; Gamm DM; Uhler MD
Biochem J; 2000 Feb; 345 Pt 3(Pt 3):673-80. PubMed ID: 10642527
[TBL] [Abstract][Full Text] [Related]
9. Gastrointestinal hamartomatous polyposis in Lkb1 heterozygous knockout mice.
Miyoshi H; Nakau M; Ishikawa TO; Seldin MF; Oshima M; Taketo MM
Cancer Res; 2002 Apr; 62(8):2261-6. PubMed ID: 11956081
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the human LKB1/STK11 gene.
Launonen V
Hum Mutat; 2005 Oct; 26(4):291-7. PubMed ID: 16110486
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.
Miyaki M; Iijima T; Hosono K; Ishii R; Yasuno M; Mori T; Toi M; Hishima T; Shitara N; Tamura K; Utsunomiya J; Kobayashi N; Kuroki T; Iwama T
Cancer Res; 2000 Nov; 60(22):6311-3. PubMed ID: 11103790
[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. Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence.
Wang ZJ; Ellis I; Zauber P; Iwama T; Marchese C; Talbot I; Xue WH; Yan ZY; Tomlinson I
J Pathol; 1999 May; 188(1):9-13. PubMed ID: 10398133
[TBL] [Abstract][Full Text] [Related]
15. Functional analysis of Peutz-Jeghers mutations reveals that the LKB1 C-terminal region exerts a crucial role in regulating both the AMPK pathway and the cell polarity.
Forcet C; Etienne-Manneville S; Gaude H; Fournier L; Debilly S; Salmi M; Baas A; Olschwang S; Clevers H; Billaud M
Hum Mol Genet; 2005 May; 14(10):1283-92. PubMed ID: 15800014
[TBL] [Abstract][Full Text] [Related]
16. Mutation of Lkb1 and p53 genes exert a cooperative effect on tumorigenesis.
Wei C; Amos CI; Stephens LC; Campos I; Deng JM; Behringer RR; Rashid A; Frazier ML
Cancer Res; 2005 Dec; 65(24):11297-303. PubMed ID: 16357136
[TBL] [Abstract][Full Text] [Related]
17. 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]
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. 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]
20. Genetic screening for Peutz-Jeghers syndrome.
Ballhausen WG; Günther K
Expert Rev Mol Diagn; 2003 Jul; 3(4):471-9. PubMed ID: 12877386
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]