244 related articles for article (PubMed ID: 12060709)
1. Role of Lkb1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis.
Jishage K; Nezu J; Kawase Y; Iwata T; Watanabe M; Miyoshi A; Ose A; Habu K; Kake T; Kamada N; Ueda O; Kinoshita M; Jenne DE; Shimane M; Suzuki H
Proc Natl Acad Sci U S A; 2002 Jun; 99(13):8903-8. PubMed ID: 12060709
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. [Peutz-Jeghers syndrome].
Miyaki M
Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Loss of the Lkb1 tumour suppressor provokes intestinal polyposis but resistance to transformation.
Bardeesy N; Sinha M; Hezel AF; Signoretti S; Hathaway NA; Sharpless NE; Loda M; Carrasco DR; DePinho RA
Nature; 2002 Sep; 419(6903):162-7. PubMed ID: 12226664
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. Induction of cyclooxygenase-2 in a mouse model of Peutz-Jeghers polyposis.
Rossi DJ; Ylikorkala A; Korsisaari N; Salovaara R; Luukko K; Launonen V; Henkemeyer M; Ristimaki A; Aaltonen LA; Makela TP
Proc Natl Acad Sci U S A; 2002 Sep; 99(19):12327-32. PubMed ID: 12218179
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
