146 related articles for article (PubMed ID: 10727082)
1. 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]
2. 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]
3. 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]
4. Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.
Wang ZJ; Churchman M; Avizienyte E; McKeown C; Davies S; Evans DG; Ferguson A; Ellis I; Xu WH; Yan ZY; Aaltonen LA; Tomlinson IP
J Med Genet; 1999 May; 36(5):365-8. PubMed ID: 10353780
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
Jenne DE; Reimann H; Nezu J; Friedel W; Loff S; Jeschke R; Müller O; Back W; Zimmer M
Nat Genet; 1998 Jan; 18(1):38-43. PubMed ID: 9425897
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers.
Su GH; Hruban RH; Bansal RK; Bova GS; Tang DJ; Shekher MC; Westerman AM; Entius MM; Goggins M; Yeo CJ; Kern SE
Am J Pathol; 1999 Jun; 154(6):1835-40. PubMed ID: 10362809
[TBL] [Abstract][Full Text] [Related]
9. Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
Ylikorkala A; Avizienyte E; Tomlinson IP; Tiainen M; Roth S; Loukola A; Hemminki A; Johansson M; Sistonen P; Markie D; Neale K; Phillips R; Zauber P; Twama T; Sampson J; Järvinen H; Mäkelä TP; Aaltonen LA
Hum Mol Genet; 1999 Jan; 8(1):45-51. PubMed ID: 9887330
[TBL] [Abstract][Full Text] [Related]
10. Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome.
Hearle NC; Tomlinson I; Lim W; Murday V; Swarbrick E; Lim G; Phillips R; Lee P; O'Donohue J; Trembath RC; Morrison PJ; Norman A; Taylor R; Hodgson S; Lucassen A; Houlston RS
BMC Genomics; 2005 Mar; 6():38. PubMed ID: 15774015
[TBL] [Abstract][Full Text] [Related]
11. Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11.
Trojan J; Brieger A; Raedle J; Roth WK; Zeuzem S
Am J Gastroenterol; 1999 Jan; 94(1):257-61. PubMed ID: 9934767
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
McKay V; Cairns D; Gokhale D; Mountford R; Greenhalgh L
Fam Cancer; 2016 Jan; 15(1):57-61. PubMed ID: 26386697
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Somatic mutations in the Peutz-Jeghers (LKB1/STKII) gene in sporadic malignant melanomas.
Rowan A; Bataille V; MacKie R; Healy E; Bicknell D; Bodmer W; Tomlinson I
J Invest Dermatol; 1999 Apr; 112(4):509-11. PubMed ID: 10201537
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Mutation analysis of STK11 gene coding region for 20 Chinese patients with Peutz-Jeghers syndrome].
Zhao X; Li Y; Ling Y; Chen H; Zhang B; Xia T; Zhou P
Nan Fang Yi Ke Da Xue Xue Bao; 2012 Apr; 32(4):511-4. PubMed ID: 22543132
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.
Mehenni H; Resta N; Guanti G; Mota-Vieira L; Lerner A; Peyman M; Chong KA; Aissa L; Ince A; Cosme A; Costanza MC; Rossier C; Radhakrishna U; Burt RW; Picard D
Dig Dis Sci; 2007 Aug; 52(8):1924-33. PubMed ID: 17404884
[TBL] [Abstract][Full Text] [Related]
20. Phosphorylation of the protein kinase mutated in Peutz-Jeghers cancer syndrome, LKB1/STK11, at Ser431 by p90(RSK) and cAMP-dependent protein kinase, but not its farnesylation at Cys(433), is essential for LKB1 to suppress cell vrowth.
Sapkota GP; Kieloch A; Lizcano JM; Lain S; Arthur JS; Williams MR; Morrice N; Deak M; Alessi DR
J Biol Chem; 2001 Jun; 276(22):19469-82. PubMed ID: 11297520
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]