๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

GLI gene and rhabdomyosarcoma

โœ Scribed by Myklebost, Ola


Book ID
109929879
Publisher
Nature Publishing Group
Year
1998
Tongue
English
Weight
316 KB
Volume
4
Category
Article
ISSN
1078-8956

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Genes, chromosomes, and rhabdomyosarcoma
โœ John Anderson; Anthony Gordon; Kathy Pritchard-Jones; Janet Shipley ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 233 KB

Rhabdomyosarcomas are a heterogeneous group of malignant tumors and are the most common soft-tissue sarcoma of childhood. Rhabdomyosarcomas resemble developing skeletal muscle, notably in their expression of the MRF family of transcription factors and the PAX3 and PAX7 genes. These PAX genes are als

MYCN gene amplification in rhabdomyosarc
โœ David Driman; Paul S. Thorner; Mark L. Greenberg; Susan Chilton-MacNeill; Jeremy ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 799 KB

Background. Amplification of the MYCN oncogene, formerly known as N-myc, has been seen in several malignant tumors, particularly neuroblastoma, where its association with a poor clinical outcome is the clearest example of a clinically relevant oncogene mutation in any human cancer. Methods. The inc

Noonan syndrome, the SOS1 gene and embry
โœ Marjolijn C. J. Jongmans; Peter M. Hoogerbrugge; Linda Hilkens; Uta Flucke; Inek ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 336 KB

## Abstract Noonan Syndrome (NS) is an autosomal dominant condition characterized by short stature, facial dysmorphisms, and congenital heart defects, and is caused by mutations in either __PTPN11, KRAS, NRAS, SHOC2, RAF1,__ or __SOS1.__ Furthermore, NS is known for its predisposition to develop ca

MAGE, BAGE and GAGE gene expression in h
โœ Piero Dalerba; Emanuela Frascella; Beatrice Macino; Susanna Mandruzzato; Annalis ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 90 KB

MAGE, BAGE and GAGE genes encode tumor-associated antigens that are presented by HLA class I molecules and recognized by CD8 ุ‰ cytolytic T lymphocytes. These antigens are currently regarded as promising targets for active, specific tumor immunotherapy because MAGE, BAGE and GAGE genes are expressed

Gli genes in development and cancer
โœ Matise, Michael P; Joyner, Alexandra L ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Nature Publishing Group ๐ŸŒ English โš– 498 KB