311 related articles for article (PubMed ID: 9809980)
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. 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]
23. 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]
24. 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]
25. 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]
26. 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]
27. 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]
28. 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]
29. 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]
30. 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]
31. Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
Kruse R; Uhlhaas S; Lamberti C; Keller KM; Jackisch C; Steinhard J; Knöpfle G; Loff S; Back W; Stolte M; Jungck M; Propping P; Friedl W; Jenne DE
Hum Mutat; 1999; 13(3):257-8. PubMed ID: 10090485
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Duodenal cancer in a patient with Peutz-Jeghers syndrome: molecular analysis.
Nakamura T; Suzuki S; Yokoi Y; Kashiwabara H; Maruyama K; Baba S; Nakagawa H; Nakamura S
J Gastroenterol; 2002; 37(5):376-80. PubMed ID: 12051537
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. The hamartoma-adenoma-carcinoma sequence.
Bosman FT
J Pathol; 1999 May; 188(1):1-2. PubMed ID: 10398131
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Inactivation of LKB1/STK11 is a common event in adenocarcinomas of the lung.
Sanchez-Cespedes M; Parrella P; Esteller M; Nomoto S; Trink B; Engles JM; Westra WH; Herman JG; Sidransky D
Cancer Res; 2002 Jul; 62(13):3659-62. PubMed ID: 12097271
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Mutational analysis of STK11 gene in ovarian carcinomas.
Nishioka Y; Kobayashi K; Sagae S; Sugimura M; Ishioka S; Nagata M; Terasawa K; Tokino T; Kudo R
Jpn J Cancer Res; 1999 Jun; 90(6):629-32. PubMed ID: 10429654
[TBL] [Abstract][Full Text] [Related]
40. Genetic heterogeneity in Peutz-Jeghers syndrome.
Boardman LA; Couch FJ; Burgart LJ; Schwartz D; Berry R; McDonnell SK; Schaid DJ; Hartmann LC; Schroeder JJ; Stratakis CA; Thibodeau SN
Hum Mutat; 2000; 16(1):23-30. PubMed ID: 10874301
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
