๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Analysis of the NF2 gene in oligodendrogliomas and ependymomas

โœ Scribed by M.Eva Alonso; M.Josefa Bello; Dolores Arjona; Pilar Gonzalez-Gomez; Jesus Lomas; Jose M de Campos; M.Elena Kusak; Alberto Isla; Juan A Rey

Book ID
114135253
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
159 KB
Volume
134
Category
Article
ISSN
0165-4608

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Exon scanning for mutations of the nf2 g
Exon scanning for mutations of the nf2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas
โœ Irene Slavc; Mia M. Maccollin; Michael Dunn; Susan Jones; Leslie Sutton; James F ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 802 KB

## Abstract Deletions of chromosome 22 have been identified in 3 types of childhood primary brain tumor: meningiomas, rhabdoid or atypical teratoid tumors (ATT) and ependymomas. This implicates the involvement of tumor suppressor genes on chromosome 22 in the genesis of these rare tumors. One such

Cytogenetic and loss of heterozygosity s
Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas
โœ David T. Ransom; Steve R. Ritland; David W. Kimmel; Cheryl A. Moertel; Richard J ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 821 KB

## Abstract Cytogenetic and/or loss of heterozygosity studies were performed on 13 ependymomas, 11 pilocytic astrocytomas, and 18 oligodendrogliomas. Loss of chromosome 22 was the most frequent genetic abnormality among the ependymomas. We found no consistent genetic abnormality in pilocytic astroc