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 *

113 related articles for article (PubMed ID: 11103795)

  • 1. The RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma.
    Chibon F; Mairal A; Fréneaux P; Terrier P; Coindre JM; Sastre X; Aurias A
    Cancer Res; 2000 Nov; 60(22):6339-45. PubMed ID: 11103795
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel gene, MASL1, within an amplicon at 8p23.1 detected in malignant fibrous histiocytomas by comparative genomic hybridization.
    Sakabe T; Shinomiya T; Mori T; Ariyama Y; Fukuda Y; Fujiwara T; Nakamura Y; Inazawa J
    Cancer Res; 1999 Feb; 59(3):511-5. PubMed ID: 9973190
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome 13q deletion mapping in pituitary tumors: infrequent loss of the retinoblastoma susceptibility gene (RB1) locus despite loss of RB1 protein product in somatotrophinomas.
    Simpson DJ; Magnay J; Bicknell JE; Barkan AL; McNicol AM; Clayton RN; Farrell WE
    Cancer Res; 1999 Apr; 59(7):1562-6. PubMed ID: 10197629
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular cytogenetic analysis in splenic lymphoma with villous lymphocytes: frequent allelic imbalance of the RB1 gene but not the D13S25 locus on chromosome 13q14.
    García-Marco JA; Nouel A; Navarro B; Matutes E; Oscier D; Price CM; Catovsky D
    Cancer Res; 1998 Apr; 58(8):1736-40. PubMed ID: 9563492
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.
    Choy KW; Pang CP; Yu CB; Wong HL; Ng JS; Fan DS; Lo KW; Chai JT; Wang J; Fu W; Lam DS
    Hum Mutat; 2002 Nov; 20(5):408. PubMed ID: 12402348
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of heterozygosity at 13q14 correlates with RB1 gene underexpression in human breast cancer.
    Bièche I; Lidereau R
    Mol Carcinog; 2000 Nov; 29(3):151-8. PubMed ID: 11108660
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Leiomyosarcomas and most malignant fibrous histiocytomas share very similar comparative genomic hybridization imbalances: an analysis of a series of 27 leiomyosarcomas.
    Derré J; Lagacé R; Nicolas A; Mairal A; Chibon F; Coindre JM; Terrier P; Sastre X; Aurias A
    Lab Invest; 2001 Feb; 81(2):211-5. PubMed ID: 11232643
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequent loss of 9p21 (p16(INK4A)) and other genomic imbalances in human malignant fibrous histiocytoma.
    Simons A; Schepens M; Jeuken J; Sprenger S; van de Zande G; Bjerkehagen B; Forus A; Weibolt V; Molenaar I; van den Berg E; Myklebost O; Bridge J; van Kessel AG; Suijkerbuijk R
    Cancer Genet Cytogenet; 2000 Apr; 118(2):89-98. PubMed ID: 10748288
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Loss of chromosome 13 is the most frequent genomic imbalance in malignant fibrous histiocytomas. A comparative genomic hybridization analysis of a series of 30 cases.
    Mairal A; Terrier P; Chibon F; Sastre X; Lecesne A; Aurias A
    Cancer Genet Cytogenet; 1999 Jun; 111(2):134-8. PubMed ID: 10347550
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.
    Brichard B; Heusterspreute M; De Potter P; Chantrain C; Vermylen C; Sibille C; Gala JL
    Eur J Cancer; 2006 Jan; 42(1):65-72. PubMed ID: 16343894
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A der(13)t(7;13)(p13;q14) with monoallelic loss of RB1 and D13S319 in myelodysplastic syndrome.
    Yamamoto K; Ito M; Minagawa K; Urahama N; Sada A; Okamura A; Matsui T
    Cancer Genet Cytogenet; 2005 Oct; 162(2):160-5. PubMed ID: 16213365
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma.
    Gratias S; Rieder H; Ullmann R; Klein-Hitpass L; Schneider S; Bölöni R; Kappler M; Lohmann DR
    Cancer Res; 2007 Jan; 67(1):408-16. PubMed ID: 17210724
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1.
    Fang Y; Elahi A; Denley RC; Rao PH; Brennan MF; Jhanwar SC
    Anticancer Res; 2009 Apr; 29(4):1255-62. PubMed ID: 19414372
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 13q deletions in B-cell lymphoproliferative disorders: frequent association with translocation.
    Struski S; Helias C; Gervais C; Audhuy B; Zamfir A; Herbrecht R; Lessard M
    Cancer Genet Cytogenet; 2007 Apr; 174(2):151-60. PubMed ID: 17452258
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An 800-kb region of deletion at 13q14 in human prostate and other carcinomas.
    Chen C; Frierson HF; Haggerty PF; Theodorescu D; Gregory CW; Dong JT
    Genomics; 2001 Oct; 77(3):135-44. PubMed ID: 11597138
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Leiomyosarcoma and malignant fibrous histiocytoma share similar allelic imbalance pattern at 9p.
    Sabah M; Cummins R; Leader M; Kay E
    Virchows Arch; 2005 Mar; 446(3):251-8. PubMed ID: 15731925
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome instability in secondary solid tumors developing after radiotherapy of bilateral retinoblastoma.
    Lefèvre SH; Vogt N; Dutrillaux AM; Chauveinc L; Stoppa-Lyonnet D; Doz F; Desjardins L; Dutrillaux B; Chevillard S; Malfoy B
    Oncogene; 2001 Dec; 20(56):8092-9. PubMed ID: 11781822
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of large chromosome markers in a malignant fibrous histiocytoma by spectral karyotyping, comparative genomic hybridization (CGH), and array CGH.
    Weng WH; Wejde J; Ahlén J; Pang ST; Lui WO; Larsson C
    Cancer Genet Cytogenet; 2004 Apr; 150(1):27-32. PubMed ID: 15041220
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of four distinct regions of allelic imbalances on chromosome 1 by the combined comparative genomic hybridization and microsatellite analysis on hepatocellular carcinoma.
    Leung TH; Wong N; Lai PB; Chan A; To KF; Liew CT; Lau WY; Johnson PJ
    Mod Pathol; 2002 Nov; 15(11):1213-20. PubMed ID: 12429801
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Does comparative genomic hybridization reveal distinct differences in DNA copy number sequence patterns between leiomyosarcoma and malignant fibrous histiocytoma?
    Larramendy ML; Gentile M; Soloneski S; Knuutila S; Böhling T
    Cancer Genet Cytogenet; 2008 Nov; 187(1):1-11. PubMed ID: 18992634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.