✦ LIBER ✦

Loss of Neurofibromin in the Leptomeningeal Astroglial Heterotopia of NF-1

✍ Scribed by Mitsuhiro Kato MD; Masashi Mizuguchi MD; Seisuke Hattori PhD; Shun Nakamura PhD; Sachio Takashima MD

Book ID: 117591827
Publisher: Elsevier Science
Year: 1998
Tongue: English
Weight: 273 KB
Volume: 18
Category: Article
ISSN: 0887-8994
DOI: 10.1016/s0887-8994(97)00202-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Loss of the Neurofibromin-NF1 Gene Produ

Loss of the Neurofibromin-NF1 Gene Product and Composite Pheochromocytoma

✍ NORIKO KIMURA; MASAYUKI FUKASE; ATSUSHI WAKITA; ITARU KIMURA 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 468 KB

Role of neurofibromin 1 (NF1) in signal

Role of neurofibromin 1 (NF1) in signal transduction mediating pacap-like neuropeptide response

📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 92 KB

Allelic Loss of the NF1 Gene in NF1-Asso

Allelic Loss of the NF1 Gene in NF1-Associated Plexiform Neurofibromas

✍ Lan Kluwe; Reinhard E Friedrich; Victor F Mautner 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 153 KB

Increased expression of the neurofibroma

Increased expression of the neurofibromatosis 1 (NF1) gene product, neurofibromin, in astrocytes in response to cerebral ischemia

✍ M.J. Giordano; D.K. Mahadeo; Y.Y. He; R.T. Geist; C. Hsu; D.H. Gutmann 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 813 KB

Tumor suppressor genes encode proteins involved in growth regulation in differentiating and proliferating cells. Previous work from our laboratory has demonstrated that the neurofibromatosis 1 (NF1) tumor suppressor gene is dramatically upregulated in astrocytes stimulated with dibutyryl cyclic AMP

Prenatal exposure to ethanol induces lep

Prenatal exposure to ethanol induces leptomeningeal heterotopia in the cerebral cortex of the rat fetus

✍ Suguru Komatsu; Hiromi Sakata-Haga; Kazuhiko Sawada; Setsuji Hisano; Yoshihiro F 📂 Article 📅 2001 🏛 Springer-Verlag 🌐 English ⚖ 231 KB

Structural and biochemical consequences

Structural and biochemical consequences of NF1 associated nontruncating mutations in the Sec14-PH module of neurofibromin

✍ Stefan Welti; Sonja Kühn; Igor D'Angelo; Britta Brügger; Dieter Kaufmann; Klaus 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 263 KB

Neurofibromatosis type 1 (NF1) is a common genetic disorder caused by alterations in the tumor suppressor gene NF1. Clinical manifestations include various neural crest derived tumors, pigmentation anomalies, bone deformations, and learning disabilities. NF1 encodes the Ras specific GTPase activatin