110 related articles for article (PubMed ID: 11004696)
1. In situ analysis of LKB1/STK11 mRNA expression in human normal tissues and tumours.
Rowan A; Churchman M; Jefferey R; Hanby A; Poulsom R; Tomlinson I
J Pathol; 2000 Oct; 192(2):203-6. PubMed ID: 11004696
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. 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]
5. 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]
6. 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]
7. 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]
8. Identification of a novel mRNA species of the LKB1/STK11 Peutz-Jeghers serine/threonine kinase.
Churchman M; Dowling B; Tomlinson IP
DNA Seq; 1999; 10(4-5):255-61. PubMed ID: 10727082
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. The tumor suppressor gene LKB1 is associated with prognosis in human breast carcinoma.
Shen Z; Wen XF; Lan F; Shen ZZ; Shao ZM
Clin Cancer Res; 2002 Jul; 8(7):2085-90. PubMed ID: 12114407
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. A role for Drosophila LKB1 in anterior-posterior axis formation and epithelial polarity.
Martin SG; St Johnston D
Nature; 2003 Jan; 421(6921):379-84. PubMed ID: 12540903
[TBL] [Abstract][Full Text] [Related]
15. LKB1: a sweet side to Peutz-Jeghers syndrome?
Carling D
Trends Mol Med; 2006 Apr; 12(4):144-7. PubMed ID: 16530014
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Specific pattern of LKB1 and phospho-acetyl-CoA carboxylase protein immunostaining in human normal tissues and lung carcinomas.
Conde E; Suarez-Gauthier A; García-García E; Lopez-Rios F; Lopez-Encuentra A; García-Lujan R; Morente M; Sanchez-Verde L; Sanchez-Cespedes M
Hum Pathol; 2007 Sep; 38(9):1351-60. PubMed ID: 17521700
[TBL] [Abstract][Full Text] [Related]
20. Lack of STK11 gene expression in homozygous twins with Peutz-Jeghers syndrome.
Tseng CJ; Chen SF; Liou SI; Lu SC; Chen JM; Sun CF; Chang SD; Cheng PJ; Liou JD; Chu DC
Ann Clin Lab Sci; 2004; 34(2):154-8. PubMed ID: 15228227
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]