𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Translocation t(9;22)(q22;q12) is a primary cytogenetic abnormality in extraskeletal myxoid chondrosarcoma

✍ Scribed by Göran Stenman; Helene Andersson; Nils Mandahl; Jeanne M. Meis-Kindblom; Lars-Gunnar Kindblom


Publisher
John Wiley and Sons
Year
1995
Tongue
French
Weight
626 KB
Volume
62
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


LPXN, a member of the paxillin superfami
✍ Hai-Ping Dai; Yong-Quan Xue; Jian-Wei Zhou; Ai-Ping Li; Ya-Fang Wu; Jin-Lan Pan; 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 342 KB 👁 1 views

## Abstract __RUNX1__ (previously __AML1__) is involved in multiple recurrent chromosomal rearrangements in hematological malignances. Recently, we identified a novel fusion between __RUNX1__ and __LPXN__ from an acute myeloid leukemia (AML) patient with t(11;21)(q12;q22). This translocation genera

EWSR1 is fused to POU5F1 in a bone tumor
✍ Shuichi Yamaguchi; Yukari Yamazaki; Yuichi Ishikawa; Noriyoshi Kawaguchi; Hiroyu 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 348 KB 👁 1 views

## Abstract __POU5F1__(OCT3/4) is a sequence‐specific transcription factor that is essential for keeping germ cells and embryonic stem cells in an immature and pluripotent status. In this article, we report that __POU5F1__ was fused to __EWSR1__ in a case of undifferentiated sarcoma derived from pe