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 *

297 related articles for article (PubMed ID: 10201537)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. Detection and analysis of common pathogenic germline mutations in Peutz-Jeghers syndrome.
    Gu GL; Zhang Z; Zhang YH; Yu PF; Dong ZW; Yang HR; Yuan Y
    World J Gastroenterol; 2021 Oct; 27(39):6631-6646. PubMed ID: 34754157
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer.
    Resta N; Simone C; Mareni C; Montera M; Gentile M; Susca F; Gristina R; Pozzi S; Bertario L; Bufo P; Carlomagno N; Ingrosso M; Rossini FP; Tenconi R; Guanti G
    Cancer Res; 1998 Nov; 58(21):4799-801. PubMed ID: 9809980
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Peutz-Jeghers syndrome].
    Miyaki M
    Nihon Rinsho; 2000 Jul; 58(7):1400-4. PubMed ID: 10921312
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma.
    Olschwang S; Boisson C; Thomas G
    J Med Genet; 2001 Jun; 38(6):356-60. PubMed ID: 11389158
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. A novel STK11 germline mutation in two siblings with Peutz-Jeghers syndrome complicated by primary gastric cancer.
    Shinmura K; Goto M; Tao H; Shimizu S; Otsuki Y; Kobayashi H; Ushida S; Suzuki K; Tsuneyoshi T; Sugimura H
    Clin Genet; 2005 Jan; 67(1):81-6. PubMed ID: 15617552
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.