BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 9288765)

  • 1. Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p.
    Amos CI; Bali D; Thiel TJ; Anderson JP; Gourley I; Frazier ML; Lynch PM; Luchtefeld MA; Young A; McGarrity TJ; Seldin MF
    Cancer Res; 1997 Sep; 57(17):3653-6. PubMed ID: 9288765
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3.
    Nakagawa H; Koyama K; Tanaka T; Miyoshi Y; Ando H; Baba S; Watatani M; Yasutomi M; Monden M; Nakamura Y
    Hum Genet; 1998 Feb; 102(2):203-6. PubMed ID: 9521590
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis.
    Hemminki A; Tomlinson I; Markie D; Järvinen H; Sistonen P; Björkqvist AM; Knuutila S; Salovaara R; Bodmer W; Shibata D; de la Chapelle A; Aaltonen LA
    Nat Genet; 1997 Jan; 15(1):87-90. PubMed ID: 8988175
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.
    Mehenni H; Blouin JL; Radhakrishna U; Bhardwaj SS; Bhardwaj K; Dixit VB; Richards KF; Bermejo-Fenoll A; Leal AS; Raval RC; Antonarakis SE
    Am J Hum Genet; 1997 Dec; 61(6):1327-34. PubMed ID: 9399902
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.
    Olschwang S; Markie D; Seal S; Neale K; Phillips R; Cottrell S; Ellis I; Hodgson S; Zauber P; Spigelman A; Iwama T; Loff S; McKeown C; Marchese C; Sampson J; Davies S; Talbot I; Wyke J; Thomas G; Bodmer W; Hemminki A; Avizienyte E; de la Chapelle A; Aaltonen L; Tomlinson I
    J Med Genet; 1998 Jan; 35(1):42-4. PubMed ID: 9475093
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
    Hearle N; Lucassen A; Wang R; Lim W; Ross F; Wheeler R; Moore I; Shipley J; Houlston R
    Genes Chromosomes Cancer; 2004 Oct; 41(2):163-9. PubMed ID: 15287029
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix.
    Lee JY; Dong SM; Kim HS; Kim SY; Na EY; Shin MS; Lee SH; Park WS; Kim KM; Lee YS; Jang JJ; Yoo NJ
    Cancer Res; 1998 Mar; 58(6):1140-3. PubMed ID: 9515797
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.
    Gruber SB; Entius MM; Petersen GM; Laken SJ; Longo PA; Boyer R; Levin AM; Mujumdar UJ; Trent JM; Kinzler KW; Vogelstein B; Hamilton SR; Polymeropoulos MH; Offerhaus GJ; Giardiello FM
    Cancer Res; 1998 Dec; 58(23):5267-70. PubMed ID: 9850045
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.
    Stratakis CA; Kirschner LS; Taymans SE; Tomlinson IP; Marsh DJ; Torpy DJ; Giatzakis C; Eccles DM; Theaker J; Houlston RS; Blouin JL; Antonarakis SE; Basson CT; Eng C; Carney JA
    J Clin Endocrinol Metab; 1998 Aug; 83(8):2972-6. PubMed ID: 9709978
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.
    Tomlinson IP; Olschwang S; Abelovitch D; Nakamura Y; Bodmer WF; Thomas G; Markie D
    Ann Hum Genet; 1996 Sep; 60(5):377-84. PubMed ID: 8912790
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome.
    Marneros AG; Mehenni H; Reichenberger E; Antonarakis SE; Krieg T; Olsen BR
    Cytogenet Cell Genet; 2001; 92(3-4):213-6. PubMed ID: 11435690
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
    Hemminki A; Markie D; Tomlinson I; Avizienyte E; Roth S; Loukola A; Bignell G; Warren W; Aminoff M; Höglund P; Järvinen H; Kristo P; Pelin K; Ridanpää M; Salovaara R; Toro T; Bodmer W; Olschwang S; Olsen AS; Stratton MR; de la Chapelle A; Aaltonen LA
    Nature; 1998 Jan; 391(6663):184-7. PubMed ID: 9428765
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
    Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC
    Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.