BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

90 related articles for article (PubMed ID: 11435690)

  • 1. 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]  

  • 2. Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2.
    Buchet-Poyau K; Mehenni H; Radhakrishna U; Antonarakis SE
    Cytogenet Genome Res; 2002; 97(3-4):171-8. PubMed ID: 12438709
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
    Mehenni H; Gehrig C; Nezu J; Oku A; Shimane M; Rossier C; Guex N; Blouin JL; Scott HS; Antonarakis SE
    Am J Hum Genet; 1998 Dec; 63(6):1641-50. PubMed ID: 9837816
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
    Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
    Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 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. [Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome].
    Mao X; Zhang Y; Wang H; Mao G; Ning S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):186-90. PubMed ID: 27060312
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 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. 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]  

  • 18. 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]  

  • 19. STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
    Wang Z; Wu B; Mosig RA; Chen Y; Ye F; Zhang Y; Gong W; Gong L; Huang F; Wang X; Nie B; Zheng H; Cui M; Wang Y; Wang J; Chen C; Polydorides AD; Zhang DY; Martignetti JA; Jiang B
    Hum Mutat; 2014 Jul; 35(7):851-8. PubMed ID: 24652667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
    Chow E; Meldrum CJ; Crooks R; Macrae F; Spigelman AD; Scott RJ
    Clin Genet; 2006 Nov; 70(5):409-14. PubMed ID: 17026623
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.