In vivo amplification of the PAX3-FKHR and PAX7-FKHR fusion genes in alveolar rhabdomyosarcoma (Q28288773)

2

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R J Davis

3

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B W Schäfer

4

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L M Nycum

5

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J A Biegel

Chromosomal translocations in human cancer.

6

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language of work or name

English

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publication date

January 1996

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published in

Human Molecular Genetics

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volume

5

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issue

1

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page(s)

15-21

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cites work

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Amplification of cellular oncogenes: a predictor of clinical outcome in human cancer

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Cytogenetic studies in subgroups of rhabdomyosarcoma

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Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma

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Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma

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The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3

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Detection of the t(2;13)(q35;q14) and PAX3-FKHR fusion in alveolar rhabdomyosarcoma by fluorescence in situ hybridization

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Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus

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Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13.

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Genomic organization of the human PAX3 gene: DNA sequence analysis of the region disrupted in alveolar rhabdomyosarcoma

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A specific chromosomal abnormality in rhabdomyosarcoma.

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Complex karyotypes in a series of pediatric osteosarcomas

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Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I

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Molecular cloning and characterization of a human PAX-7 cDNA expressed in normal and neoplastic myocytes

21 January 2018

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Human proto-oncogene N-myc encodes nuclear proteins that bind DNA

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Complementary homeo protein gradients in developing limb buds

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