𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Schwann cell heterogeneity—Might it underlie the diversity seen in schwann cell tumors?

✍ Scribed by Steven A. Moore

Book ID
116083494
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
107 KB
Volume
25
Category
Article
ISSN
1532-8392

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

How does the Schwann cell lineage form t
How does the Schwann cell lineage form tumors in NF1?
✍ Steven L. Carroll; Nancy Ratner 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 812 KB

## Abstract Neurofibromas are benign tumors of peripheral nerve that occur sporadically or in patients with the autosomal dominant tumor predisposition syndrome neurofibromatosis type 1 (NF1). Multiple neurofibroma subtypes exist which differ in their site of occurrence, their association with NF1,

A mouse embryonic stem cell model of Sch
A mouse embryonic stem cell model of Schwann cell differentiation for studies of the role of neurofibromatosis type 1 in Schwann cell development and tumor formation
✍ Therese M. Roth; Poornapriya Ramamurthy; Fumi Ebisu; Robert P. Lisak; Beverly M. 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 741 KB

## Abstract The neurofibromatosis Type 1 (NF1) gene functions as a tumor suppressor gene. One known function of neurofibromin, the NF1 protein product, is to accelerate the slow intrinsic GTPase activity of Ras to increase the production of inactive rasGDP, with wide‐ranging effects on p21ras pathw

Plexiform-like neurofibromas develop in
Plexiform-like neurofibromas develop in the mouse by intraneural xenograft of an NF1 tumor-derived Schwann cell line
✍ George Q. Perrin; Lauren Fishbein; Susanne A. Thomson; Stacey L. Thomas; Karen S 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 440 KB 👁 1 views

## Abstract Plexiform neurofibromas are peripheral nerve sheath tumors that arise frequently in neurofibromatosis type 1 (NF1) and have a risk of malignant progression. Past efforts to establish xenograft models for neurofibroma involved the implantation of tumor fragments or heterogeneous primary