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Post-genomic approaches to exploring neuropeptide gene mis-expression in disease

✍ Scribed by Alasdair MacKenzie; John P Quinn

Book ID: 113824221
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 653 KB
Volume: 38
Category: Article
ISSN: 0143-4179
DOI: 10.1016/j.npep.2003.09.004

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## Abstract Rhabdomyosarcomas (RMS) are the most common pediatric soft tissue sarcomas. They resemble developing skeletal muscle and are histologically divided into two main subtypes; alveolar and embryonal RMS. Characteristic genomic aberrations, including the __PAX3__‐ and __PAX7‐FOXO1__ fusion g