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 *

439 related articles for article (PubMed ID: 9233770)

  • 1. Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours.
    Vorechovský I; Tingby O; Hartman M; Strömberg B; Nister M; Collins VP; Toftgård R
    Oncogene; 1997 Jul; 15(3):361-6. PubMed ID: 9233770
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.
    Wolter M; Reifenberger J; Sommer C; Ruzicka T; Reifenberger G
    Cancer Res; 1997 Jul; 57(13):2581-5. PubMed ID: 9205058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. No evidence for mutations or altered expression of the Suppressor of Fused gene (SUFU) in primitive neuroectodermal tumours.
    Koch A; Waha A; Hartmann W; Milde U; Goodyer CG; Sörensen N; Berthold F; Digon-Söntgerath B; Krätzschmar J; Wiestler OD; Pietsch T
    Neuropathol Appl Neurobiol; 2004 Oct; 30(5):532-9. PubMed ID: 15488029
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors.
    Xie J; Johnson RL; Zhang X; Bare JW; Waldman FM; Cogen PH; Menon AG; Warren RS; Chen LC; Scott MP; Epstein EH
    Cancer Res; 1997 Jun; 57(12):2369-72. PubMed ID: 9192811
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.
    Vortmeyer AO; Stavrou T; Selby D; Li G; Weil RJ; Park WS; Moon YW; Chandra R; Goldstein AM; Zhuang Z
    Cancer; 1999 Jun; 85(12):2662-7. PubMed ID: 10375116
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in SUFU predispose to medulloblastoma.
    Taylor MD; Liu L; Raffel C; Hui CC; Mainprize TG; Zhang X; Agatep R; Chiappa S; Gao L; Lowrance A; Hao A; Goldstein AM; Stavrou T; Scherer SW; Dura WT; Wainwright B; Squire JA; Rutka JT; Hogg D
    Nat Genet; 2002 Jul; 31(3):306-10. PubMed ID: 12068298
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas.
    Schofield D; West DC; Anthony DC; Marshal R; Sklar J
    Am J Pathol; 1995 Feb; 146(2):472-80. PubMed ID: 7856756
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for GAS1 and PTC mutations.
    Simoneau AR; Spruck CH; Gonzalez-Zulueta M; Gonzalgo ML; Chan MF; Tsai YC; Dean M; Steven K; Horn T; Jones PA
    Cancer Res; 1996 Nov; 56(21):5039-43. PubMed ID: 8895761
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Missense mutations in SMOH in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.
    Reifenberger J; Wolter M; Weber RG; Megahed M; Ruzicka T; Lichter P; Reifenberger G
    Cancer Res; 1998 May; 58(9):1798-803. PubMed ID: 9581815
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma.
    Maesawa C; Tamura G; Iwaya T; Ogasawara S; Ishida K; Sato N; Nishizuka S; Suzuki Y; Ikeda K; Aoki K; Saito K; Satodate R
    Genes Chromosomes Cancer; 1998 Mar; 21(3):276-9. PubMed ID: 9523206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of PTCH/SMO/SHH pathway genes in medulloblastoma.
    Zurawel RH; Allen C; Chiappa S; Cato W; Biegel J; Cogen P; de Sauvage F; Raffel C
    Genes Chromosomes Cancer; 2000 Jan; 27(1):44-51. PubMed ID: 10564585
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Status of the DPC4 tumor suppressor gene in sporadic colon adenocarcinoma of Croatian patients: identification of a novel somatic mutation.
    Popović Hadzija M; Radosevic S; Kovacević D; Lukac J; Hadzija M; Spaventi R; Pavelić K; Kapitanović S
    Mutat Res; 2004 Apr; 548(1-2):61-73. PubMed ID: 15063137
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The patched/hedgehog/smoothened signalling pathway in human breast cancer: no evidence for H133Y SHH, PTCH and SMO mutations.
    Vorechovský I; Benediktsson KP; Toftgård R
    Eur J Cancer; 1999 May; 35(5):711-3. PubMed ID: 10505029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Somatic mutations of WNT/wingless signaling pathway components in primitive neuroectodermal tumors.
    Koch A; Waha A; Tonn JC; Sörensen N; Berthold F; Wolter M; Reifenberger J; Hartmann W; Friedl W; Reifenberger G; Wiestler OD; Pietsch T
    Int J Cancer; 2001 Aug; 93(3):445-9. PubMed ID: 11433413
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of the lissencephaly gene 1 (LIS-1) in medulloblastomas.
    Koch A; Tonn J; Kraus JA; Sorensen N; Albrecht NS; Wiestler OD; Pietsch T
    Neuropathol Appl Neurobiol; 1996 Jun; 22(3):233-42. PubMed ID: 8804025
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation.
    Unden AB; Holmberg E; Lundh-Rozell B; Stähle-Bäckdahl M; Zaphiropoulos PG; Toftgård R; Vorechovsky I
    Cancer Res; 1996 Oct; 56(20):4562-5. PubMed ID: 8840960
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deletions of AXIN1, a component of the WNT/wingless pathway, in sporadic medulloblastomas.
    Dahmen RP; Koch A; Denkhaus D; Tonn JC; Sörensen N; Berthold F; Behrens J; Birchmeier W; Wiestler OD; Pietsch T
    Cancer Res; 2001 Oct; 61(19):7039-43. PubMed ID: 11585731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Absence of detectable alterations in the putative tumor suppressor gene BTRC in cerebellar medulloblastomas and cutaneous basal cell carcinomas.
    Wolter M; Scharwächter C; Reifenberger J; Koch A; Pietsch T; Reifenberger G
    Acta Neuropathol; 2003 Oct; 106(4):287-90. PubMed ID: 12898158
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No evidence for the H133Y mutation in SONIC HEDGEHOG in a collection of common tumour types.
    Wicking C; Evans T; Henk B; Hayward N; Simms LA; Chenevix-Trench G; Pietsch T; Wainwright B
    Oncogene; 1998 Feb; 16(8):1091-3. PubMed ID: 9519883
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sporadic medulloblastomas contain PTCH mutations.
    Raffel C; Jenkins RB; Frederick L; Hebrink D; Alderete B; Fults DW; James CD
    Cancer Res; 1997 Mar; 57(5):842-5. PubMed ID: 9041183
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.