225 related articles for article (PubMed ID: 15021901)
21. 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]
22. 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]
23. 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]
24. 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]
25. 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]
26. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. No evidence for germline mutations of the LKB1/STK11 gene in familial pancreatic carcinoma.
Grützmann R; McFaul C; Bartsch DK; Sina-Frey M; Rieder H; Koch R; McCarthy E; Greenhalf W; Neoptolemos JP; Saeger HD; Pilarsky C
Cancer Lett; 2004 Oct; 214(1):63-8. PubMed ID: 15331174
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Bronchioloalveolar carcinoma: a new cancer in Peutz-Jeghers syndrome.
von Herbay A; Arens N; Friedl W; Vogt-Moykopf I; Kayser K; Müller KM; Back W
Lung Cancer; 2005 Feb; 47(2):283-8. PubMed ID: 15639728
[TBL] [Abstract][Full Text] [Related]
31. Genetic and epigenetic screening for gene alterations of the chromatin-remodeling factor, SMARCA4/BRG1, in lung tumors.
Medina PP; Carretero J; Fraga MF; Esteller M; Sidransky D; Sanchez-Cespedes M
Genes Chromosomes Cancer; 2004 Oct; 41(2):170-7. PubMed ID: 15287030
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Loss of Lkb1 provokes highly invasive endometrial adenocarcinomas.
Contreras CM; Gurumurthy S; Haynie JM; Shirley LJ; Akbay EA; Wingo SN; Schorge JO; Broaddus RR; Wong KK; Bardeesy N; Castrillon DH
Cancer Res; 2008 Feb; 68(3):759-66. PubMed ID: 18245476
[TBL] [Abstract][Full Text] [Related]
34. Dysfunctional AMPK activity, signalling through mTOR and survival in response to energetic stress in LKB1-deficient lung cancer.
Carretero J; Medina PP; Blanco R; Smit L; Tang M; Roncador G; Maestre L; Conde E; Lopez-Rios F; Clevers HC; Sanchez-Cespedes M
Oncogene; 2007 Mar; 26(11):1616-25. PubMed ID: 16953221
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Hepatocellular carcinoma caused by loss of heterozygosity in Lkb1 gene knockout mice.
Nakau M; Miyoshi H; Seldin MF; Imamura M; Oshima M; Taketo MM
Cancer Res; 2002 Aug; 62(16):4549-53. PubMed ID: 12183403
[TBL] [Abstract][Full Text] [Related]
38. Molecular mechanisms of tumor suppression by LKB1.
Vaahtomeri K; Mäkelä TP
FEBS Lett; 2011 Apr; 585(7):944-51. PubMed ID: 21192934
[TBL] [Abstract][Full Text] [Related]
39. LKB1; linking cell structure and tumor suppression.
Hezel AF; Bardeesy N
Oncogene; 2008 Nov; 27(55):6908-19. PubMed ID: 19029933
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
