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Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein

Author

Stephen Friend

Published in: Proceedings of the National Academy of Sciences of the United States of America

Date of publication: December 1, 1987

Language: English

Main subject: retinoblastoma

Bibliographic databases:

Cites articles 32

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A strategy to reveal high-frequency RFLPs along the human X chromosome
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Retinoblastoma: clues to human oncogenesis,Retinoblastoma: Clues to Human Oncogenesis
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A rapid single-stranded cloning strategy for producing a sequential series of overlapping clones for use in DNA sequencing: application to sequencing the corn mitochondrial 18 S rDNA
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Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition
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Protein-tyrosine kinases
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Second malignant neoplasms in children: an update from the Late Effects Study Group
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The refined structure of vitamin D-dependent calcium-binding protein from bovine intestine. Molecular details, ion binding, and implications for the structure of other calcium-binding proteins
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Second primary neoplasms in patients with retinoblastoma
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Chromosome 13 homozygosity in osteosarcoma without retinoblastoma
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A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
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Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas
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Potential metal-binding domains in nucleic acid binding proteins
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Retinoblastoma, melanoma, and pancreatic cancer
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A transcript from a Drosophila pattern gene predicts a protein homologous to the transforming growth factor-beta family
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Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13
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Structural evidence for the authenticity of the human retinoblastoma gene

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