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 *

388 related articles for article (PubMed ID: 16682285)

  • 1. A molecular study of first and second RB1 mutational hits in retinoblastoma patients.
    de Andrade AF; da Hora Barbosa R; Vargas FR; Ferman S; Eisenberg AL; Fernandes L; Bonvicino CR
    Cancer Genet Cytogenet; 2006 May; 167(1):43-6. PubMed ID: 16682285
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.
    Hogg A; Onadim Z; Baird PN; Cowell JK
    Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of four novel RB1 germline mutations in Korean retinoblastoma patients.
    Yu YS; Kim IJ; Ku JL; Park JG
    Hum Mutat; 2001 Sep; 18(3):252. PubMed ID: 11524739
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Spectrum and frequencies of RB1 gene structural defects in retinoblastoma].
    Babenko OV; Saakian SV; Brovkina AF; Kozlova VM; Strel'nikov VV; Zaletaev DV; Nemtsova MV
    Mol Biol (Mosk); 2002; 36(4):623-9. PubMed ID: 12173465
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutations.
    Kiran VS; Kannabiran C; Chakravarthi K; Vemuganti GK; Honavar SG
    Hum Mutat; 2003 Oct; 22(4):339. PubMed ID: 12955724
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
    Nichols KE; Houseknecht MD; Godmilow L; Bunin G; Shields C; Meadows A; Ganguly A
    Hum Mutat; 2005 Jun; 25(6):566-74. PubMed ID: 15884040
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening for RB1 mutations in tumor tissue using denaturing high performance liquid chromatography, multiplex ligation-dependent probe amplification, and loss of heterozygosity analysis.
    Sellner LN; Edkins E; Smith N
    Pediatr Dev Pathol; 2006; 9(1):31-7. PubMed ID: 16808635
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.
    Alonso J; Frayle H; Menéndez I; López A; García-Miguel P; Abelairas J; Sarret E; Vendrell MT; Navajas A; Artigas M; Indiano JM; Carbone A; Torrenteras C; Palacios I; Pestaña A
    Hum Mutat; 2005 Jan; 25(1):99. PubMed ID: 15605413
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletions of chromosome 13q, mutations in Retinoblastoma 1, and retinoblastoma protein state in human hepatocellular carcinoma.
    Zhang X; Xu HJ; Murakami Y; Sachse R; Yashima K; Hirohashi S; Hu SX; Benedict WF; Sekiya T
    Cancer Res; 1994 Aug; 54(15):4177-82. PubMed ID: 8033150
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML; Yunis JJ
    Biomedica; 2013; 33(1):53-61. PubMed ID: 23715307
    [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. [RB1 and CDKN2A functional defects resulting in retinoblastoma].
    Babenko OV; Zemliakova VV; Saakian SV; Brovkina AF; Strel'nikov VV; Zaletaev DV; Nemtsova MV
    Mol Biol (Mosk); 2002; 36(5):777-83. PubMed ID: 12391839
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Preferential germline mutation of the paternal allele in retinoblastoma.
    Zhu XP; Dunn JM; Phillips RA; Goddard AD; Paton KE; Becker A; Gallie BL
    Nature; 1989 Jul; 340(6231):312-3. PubMed ID: 2568588
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient.
    Alonso J; Menéndez I; López A; Frayle H; Ruisánchez N; Pestaña A
    Genes Chromosomes Cancer; 2004 Jul; 40(3):271-5. PubMed ID: 15139006
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression.
    Albrecht P; Ansperger-Rescher B; Schüler A; Zeschnigk M; Gallie B; Lohmann DR
    Hum Mutat; 2005 Nov; 26(5):437-45. PubMed ID: 16127685
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of mosaic RB1 mutations in families with retinoblastoma.
    Rushlow D; Piovesan B; Zhang K; Prigoda-Lee NL; Marchong MN; Clark RD; Gallie BL
    Hum Mutat; 2009 May; 30(5):842-51. PubMed ID: 19280657
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ten novel RB1 gene mutations in patients with retinoblastoma.
    Abouzeid H; Munier FL; Thonney F; Schorderet DF
    Mol Vis; 2007 Sep; 13():1740-5. PubMed ID: 17960112
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.