186 related articles for article (PubMed ID: 16407837)
1. A novel mutation of STK11/LKB1 gene leads to the loss of cell growth inhibition in head and neck squamous cell carcinoma.
Qiu W; Schönleben F; Thaker HM; Goggins M; Su GH
Oncogene; 2006 May; 25(20):2937-42. PubMed ID: 16407837
[TBL] [Abstract][Full Text] [Related]
2. Genetic alterations of the LKB1 gene in head and neck cancer.
Kenanli E; Karaman E; Enver O; Ulutin T; Buyru N
DNA Cell Biol; 2010 Dec; 29(12):735-8. PubMed ID: 20818976
[TBL] [Abstract][Full Text] [Related]
3. Familial head and neck cancer: molecular analysis of a new clinical entity.
Yu KK; Zanation AM; Moss JR; Yarbrough WG
Laryngoscope; 2002 Sep; 112(9):1587-93. PubMed ID: 12352668
[TBL] [Abstract][Full Text] [Related]
4. LKB1 downregulation may be independent of promoter methylation or FOXO3 expression in head and neck cancer.
Ekizoglu S; Dalay N; Karaman E; Akdeniz D; Ozaydin A; Buyru N
Transl Res; 2013 Aug; 162(2):122-9. PubMed ID: 23810581
[TBL] [Abstract][Full Text] [Related]
5. Frequent loss of heterozygosity at the 19p13.3 locus without LKB1/STK11 mutations in human carcinoma metastases to the brain.
Sobottka SB; Haase M; Fitze G; Hahn M; Schackert HK; Schackert G
J Neurooncol; 2000 Sep; 49(3):187-95. PubMed ID: 11212897
[TBL] [Abstract][Full Text] [Related]
6. Disruption of transforming growth factor beta-Smad signaling pathway in head and neck squamous cell carcinoma as evidenced by mutations of SMAD2 and SMAD4.
Qiu W; Schönleben F; Li X; Su GH
Cancer Lett; 2007 Jan; 245(1-2):163-70. PubMed ID: 16478646
[TBL] [Abstract][Full Text] [Related]
7. Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p.
Chen J; Lindblom A
Clin Genet; 2000 May; 57(5):394-7. PubMed ID: 10852375
[TBL] [Abstract][Full Text] [Related]
8. STK11/LKB1 Peutz-Jeghers gene inactivation in intraductal papillary-mucinous neoplasms of the pancreas.
Sato N; Rosty C; Jansen M; Fukushima N; Ueki T; Yeo CJ; Cameron JL; Iacobuzio-Donahue CA; Hruban RH; Goggins M
Am J Pathol; 2001 Dec; 159(6):2017-22. PubMed ID: 11733352
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. PIK3CA mutations in head and neck squamous cell carcinoma.
Qiu W; Schönleben F; Li X; Ho DJ; Close LG; Manolidis S; Bennett BP; Su GH
Clin Cancer Res; 2006 Mar; 12(5):1441-6. PubMed ID: 16533766
[TBL] [Abstract][Full Text] [Related]
12. 5'-CpG island methylation of the LKB1/STK11 promoter and allelic loss at chromosome 19p13.3 in sporadic colorectal cancer.
Trojan J; Brieger A; Raedle J; Esteller M; Zeuzem S
Gut; 2000 Aug; 47(2):272-6. PubMed ID: 10896921
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Negative Regulation of Serine Threonine Kinase 11 (STK11) through miR-100 in Head and Neck Cancer.
Figueroa-González G; Carrillo-Hernández JF; Perez-Rodriguez I; Cantú de León D; Campos-Parra AD; Martínez-Gutiérrez AD; Coronel-Hernández J; García-Castillo V; López-Camarillo C; Peralta-Zaragoza O; Jacobo-Herrera NJ; Guardado-Estrada M; Pérez-Plasencia C
Genes (Basel); 2020 Sep; 11(9):. PubMed ID: 32911741
[TBL] [Abstract][Full Text] [Related]
16. The STK11/LKB1 Peutz-Jegher gene is not involved in the pathogenesis of sporadic sex cord-stromal tumors, although loss of heterozygosity at 19p13.3 indicates other gene alteration in these tumors.
Kato N; Romero M; Catasus L; Prat J
Hum Pathol; 2004 Sep; 35(9):1101-4. PubMed ID: 15343512
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Localization-specific LKB1 loss in head and neck squamous cell carcinoma metastasis.
Kline ER; Muller S; Pan L; Tighiouart M; Chen ZG; Marcus AI
Head Neck; 2011 Oct; 33(10):1501-12. PubMed ID: 21928424
[TBL] [Abstract][Full Text] [Related]
20. The ARF-p16 gene locus in carcinogenesis and therapy of head and neck squamous cell carcinoma.
Yarbrough WG
Laryngoscope; 2002 Dec; 112(12):2114-28. PubMed ID: 12461329
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]