✦ LIBER ✦

Chromosome 1p36 and 22qter deletions in paraffin block sections of intracranial meningiomas

✍ Scribed by Zerrin Yilmaz; Feride Iffet Sahin; Basar Atalay; Özlem Özen; Hakan Caner; Murad Bavbek; Beyhan Demirhan; Nur Altinörs

Publisher: Springer Netherlands
Year: 2005
Tongue: English
Weight: 90 KB
Volume: 11
Category: Article
ISSN: 1219-4956
DOI: 10.1007/bf02893855

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Detection of 1p36 deletions in paraffin

Detection of 1p36 deletions in paraffin sections of neuroblastoma tissues

✍ Cornelia Stock; Inge M. Ambros; Georg Mann; Helmut Gadner; Gabriele Amann; Peter 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 703 KB

Nonradioactive in situ hybridization (NISH) on sections of paraffin-embedded neuroblastoma tissue was performed to evaluate numerical and structural aberrations of chromosome I. Two biotinylated probes specific for the heterochromatic (D I Z I) and subtelomeric regions of chromosome I (DIS32) were u

1p and 3p deletions in meningiomas witho

1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization

✍ Katrin M. Carlson; Carl Bruder; Magnus Nordenskjöld; Jan P. Dumanski 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 78 KB 👁 2 views

Meningioma is a common tumor of the meninges covering the central nervous system. Although generally a benign tumor, meningioma often recurs and is malignant in 5-10% of all cases. Loss of chromosome 22 loci, and specifically inactivation of the NF2 tumor suppressor gene, is considered one of severa

Cytogenetic and molecular analysis of a

Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22

✍ Christophe Rosty; Martine Peter; Jessica Zucman; Pierre Validire; Olivier Delatt 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 281 KB 👁 2 views

Malignant rhabdoid tumors are rare and aggressive neoplasms of childhood, occurring in the kidney or in various extrarenal locations. Most cytogenetic studies of these tumors have shown the frequent involvement of chromosome 22, including translocations and/or deletions, with a critical region for a