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Translational Research
Volume 156, Issue 2
, Pages 91-97
, August 2010
Using RB1 mutations to assess minimal residual disease in metastatic retinoblastoma
References
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- Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma. Am J Hum Genet. 2003;72:253–269
- Detection of mosaic RB1 mutations in families with retinoblastoma. Hum Mutat. 2009;30:842–851
- Combining cyclosporin with chemotherapy controls intraocular retinoblastoma without requiring radiation. Clin Cancer Res. 1996;2:1499–1508
- Chemotherapy with focal therapy can cure intraocular retinoblastoma without radiotherapy. Arch Ophthalmol. 1996;114:1321–1328
- . Chemosensitivity and multidrug resistance to antineoplastic drugs in retinoblastoma cell lines. Anticancer Res. 1989;9:469–474
- Phase I clinical trial of intrathecal topotecan in patients with neoplastic meningitis. J Clin Oncol. 2003;21:143–147
- . Screening for hepatocellular carcinoma in patients with cirrhosis in the United States: results of a national survey. Am J Gastroenterol. 1999;94:2224–2229
- Effect of the Philadelphia chromosome on minimal residual disease in acute lymphoblastic leukemia. Leukemia. 1997;11:1497–1500
- Quantitation of minimal residual disease in Philadelphia chromosome positive chronic myeloid leukaemia patients using real-time quantitative RT-PCR. Br J Haematol. 1998;102:768–774
- Profiling genomic copy number changes in retinoblastoma beyond loss of RB1. Genes Chromosomes Cancer. 2007;46:118–129
Supported by grants from The Ontario Institute for Cancer Research and from the Canadian Retinoblastoma Society and the Royal Arch Masons of Canada. Funded in part by the Ontario Ministry of Health and Long Term Care (OMOHLTC). The views expressed do not necessarily reflect those of the OMOHLTC.
PII: S1931-5244(10)00115-5
doi: 10.1016/j.trsl.2010.05.009
© 2010 Mosby, Inc. All rights reserved.
« Previous
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Translational Research
Volume 156, Issue 2
, Pages 91-97
, August 2010
