In Vivo Amplification of the PAX3-FKHR and PAX7-FKHR Fusion Genes in Alveolar Rhabdomyosarcoma

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.5, Iss.1, 1996-01, pp. : 15-21

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Transgenic mice expressing PAX3-FKHR have multiple defects in muscle development, including ectopic skeletal myogenesis in the developing neural tube

By Finckenstein Friedrich Davicioni Elai Osborn Kent Cavenee Webster Arden Karen Anderson Michael

Transgenic Research, Vol. 15, Iss. 5, 2006-10 ,pp. : 595-614

Springer Publishing Company

Access to resources Recommend Favorite

Interaction among SOX10 , PAX3 and MITF , three genes altered in Waardenburg syndrome

By Bondurand Nadege Pingault Veronique Goerich DerkE. Lemort Nicole Sock Elisabeth Caignec Cedric Le Wegner Michael Goossens Michel

Human Molecular Genetics, Vol. 9, Iss. 13, 2000-08 ,pp. : 1907-1917

Oxford University Press

Access to resources Recommend Favorite

Pax6 3′ deletion results in aniridia, autism and mental retardation

By Davis L. Meyer K. Rudd D. Librant A. Epping E. Sheffield V. Wassink T.

Human Genetics, Vol. 123, Iss. 4, 2008-05 ,pp. : 371-378

Springer Publishing Company

Access to resources Recommend Favorite

PAX6 in sensory development

By van Heyningen V. Williamson K.A.

Human Molecular Genetics, Vol. 11, Iss. 10, 2002-05 ,pp. : 1161-1167

Oxford University Press

Access to resources Recommend Favorite

Pax2 regulates a fadd -dependent molecular switch that drives tissue fusion during eye development

By Viringipurampeer Ishaq A. Ferreira Todd DeMaria Shannon Yoon Jookyung J. Shan Xianghong Moosajee Mariya Gregory-Evans Kevin Ngai John Gregory-Evans Cheryl Y.

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2357-2369

Oxford University Press

Access to resources Recommend Favorite