These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

87 related articles for article (PubMed ID: 19250387)

  • 1. Two novel LKB1 mutations in Colombian Peutz-Jeghers syndrome patients.
    Vélez A; Gaitan MH; Marquez JR; Castaño A; Restrepo JI; Jaramillo S; Gamarra A; Novelli M; Echeverry MM; Tomlinson I; Carvajal-Carmona LG
    Clin Genet; 2009 Mar; 75(3):304-6. PubMed ID: 19250387
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 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. 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. An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites.
    Hastings ML; Resta N; Traum D; Stella A; Guanti G; Krainer AR
    Nat Struct Mol Biol; 2005 Jan; 12(1):54-9. PubMed ID: 15608654
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [Mutation screening of LKB1 gene in familial Peutz-Jeghers syndrome patients].
    Chen CY; Zhang XM; Wang FY; Wang ZK; Zhu M; Ma GJ; Zhang YY; Jin XX; Shi H; Liu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):121-5. PubMed ID: 22487816
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.
    Liu L; Du X; Nie J
    Clin Res Hepatol Gastroenterol; 2011 Mar; 35(3):221-6. PubMed ID: 21411391
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Frequent somatic mutations in serine/threonine kinase 11/Peutz-Jeghers syndrome gene in left-sided colon cancer.
    Dong SM; Kim KM; Kim SY; Shin MS; Na EY; Lee SH; Park WS; Yoo NJ; Jang JJ; Yoon CY; Kim JW; Kim SY; Yang YM; Kim SH; Kim CS; Lee JY
    Cancer Res; 1998 Sep; 58(17):3787-90. PubMed ID: 9731485
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer.
    Bignell GR; Barfoot R; Seal S; Collins N; Warren W; Stratton MR
    Cancer Res; 1998 Apr; 58(7):1384-6. PubMed ID: 9537235
    [TBL] [Abstract][Full Text] [Related]  

  • 20. No evidence of Peutz-Jeghers syndrome gene LKB1 involvement in left-sided colorectal carcinomas.
    Launonen V; Avizienyte E; Loukola A; Laiho P; Salovaara R; Järvinen H; Mecklin JP; Oku A; Shimane M; Kim HC; Kim JC; Nezu J; Aaltonen LA
    Cancer Res; 2000 Feb; 60(3):546-8. PubMed ID: 10676634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.