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B. Horsthemke (1992)
Genetics and cytogenetics of retinoblastoma.Cancer genetics and cytogenetics, 63 1
S. Griegel, Chen Hong, Roland Frötschl, D. Hülser, V. Greger, Bemhard Horsthemke, M. Rajewsky (1990)
Newly established human retinoblastoma cell lines exhibit an “immortalized” but not an invasive phenotype in vitroInternational Journal of Cancer, 46
V. Greger, S. Kerst, E. Messmer, W. Höpping, Eberhard Passarge, B. Horsthemke (1988)
Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma.Journal of Medical Genetics, 25
J. Wiggs, M. Nordenskjöld, D. Yandell, J. Rapaport, V. Grondin, M. Janson, B. Werelius, R. Petersen, A. Craft, K. Riedel (1988)
Prediction of the risk of hereditary retinoblastoma, using DNA polymorphisms within the retinoblastoma gene.The New England journal of medicine, 318 3
C. Belka, V. Greger, B. Zabel, B. Horsthemke (1991)
No evidence for sequences structurally related to the RB1 gene in the human genomeHuman Genetics, 86
L. Kunkel, Kirby Smith, S. Boyer, D. Borgaonkar, S. Wachtel, O. Miller, W. Breg, H. Jones, J. Rary (1977)
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.Proceedings of the National Academy of Sciences of the United States of America, 74 3
Junya Toguchida, T. McGee, Jennifer Paterson, Janine Eagle, Stephanie Tucker, D. Yandell, T. Dryja (1993)
Complete genomic sequence of the human retinoblastoma susceptibility gene.Genomics, 17 3
V. Greger, E. Passarge, W. Höpping, E. Messmer, B. Horsthemke (1989)
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastomaHuman Genetics, 83
R. Reis, S. Goldstein (1982)
Interclonal variation in methylation patterns for expressed and non-expressed genes.Nucleic acids research, 10 14
T. Sakai, J. Toguchida, N. Ohtani, D. Yandell, J. Rapaport, T. Dryja (1991)
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene.American journal of human genetics, 48 5
N. Ohtani‐Fujita, T. Fujita, A. Aoike, N. Osifchin, P. Robbins, T. Sakai (1993)
CpG methylation inactivates the promoter activity of the human retinoblastoma tumor-suppressor gene.Oncogene, 8 4
Kai Kloss, Petra Währisch, V. Greger, E. Messmer, H. Fritze, W. Höpping, Eberhard Passarge, B. Horsthemke (1991)
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.American journal of medical genetics, 39 2
R. Holliday (1987)
The inheritance of epigenetic defects.Science, 238 4824
D. Lohmann, B. Horsthemke, G. Gillessen‐Kaesbach, F. Stefani, H. Höfler (1992)
Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresisHuman Genetics, 89
H. Cedar (1988)
DNA methylation and gene activityCell, 53
T. McGee, D. Yandell, T. Dryja (1989)
Structure and partial genomic sequence of the human retinoblastoma susceptibility gene.Gene, 80 1
Adelaide Carothers, G. Urlaub, J. Mucha, Dezider Grunberger, L. Chasin (1989)
Point mutation analysis in a mammalian gene: rapid preparation of total RNA, PCR amplification of cDNA, and Taq sequencing by a novel method.BioTechniques, 7 5
R. Bookstein, E. Lee, H. To, L. Young, T. Sery, R. Hayes, T. Friedmann, W. Lee (1988)
Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants.Proceedings of the National Academy of Sciences of the United States of America, 85 7
The retinoblastoma susceptibility (RB1) gene contains an unmethylated CpG-rich island at its 5′ end. Using methylation-sensitive restriction enzymes, we have investigated the methylation status of this island in 21 sporadic unilateral retinoblastomas and 30 hereditary retinoblastomas. Three sporadic unilateral tumors were found to have hypermethylated RB1 alleles. In two tumors, the paternal allele was methylated, whereas the maternal allele had been lost. Cultured cells from one of these tumors were studied by the reverse transcription polymerase chain reaction and found to have a reduced level of RB1 mRNA. The third tumor had retained constitutional heterozygosity, and the paternal allele was specifically methylated. The combined data from previously published reports and from this study show that hypermethylation of the RB1 gene occurs in 13% of sporadic unilateral tumors and may reduce gene activity.
Human Genetics – Springer Journals
Published: Jul 17, 2004
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