✦ LIBER ✦

Frequent Loss of 1p32 Region but no Mutation if the p18 Tumor Suppressor Gene in Meningiomas

✍ Scribed by Pascal Leuraud; Yannick Marie; Eric Robin; Stéphanie Huguet; Jié He; Karima Mokhtari; Philippe Cornu; Khê Hoang-Xuan; Marc Sanson

Book ID: 110235009
Publisher: Springer US
Year: 2000
Tongue: English
Weight: 67 KB
Volume: 50
Category: Article
ISSN: 0167-594X
DOI: 10.1023/a:1006400723490

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Loss of Expression of the p16 Tumor Supp

Loss of Expression of the p16 Tumor Suppressor Gene Is More Frequent in Advanced Ovarian Cancers Lacking p53 Mutations

✍ Laura J. Havrilesky; Angeles A. Alvarez; Regina S. Whitaker; Jeffrey R. Marks; A 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 401 KB

Mutations of the p53 tumor-suppressor ge

Mutations of the p53 tumor-suppressor gene are frequently involved during bovine leukemia virus (BLV) induced leukemogenesis in cattle but not in sheep

✍ F. Dequiedt; L. Willems; A. Burny; R. Kettmann 📂 Article 📅 1995 🏛 Springer-Verlag 🌐 English ⚖ 154 KB

Deletion of the p53 tumor suppressor gen

Deletion of the p53 tumor suppressor gene improves neuromotor function but does not attenuate regional neuronal cell loss following experimental brain trauma in mice

✍ Gregor Tomasevic; Ramesh Raghupathi; Uwe Scherbel; Tadeusz Wieloch; Tracy K. McI 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 292 KB

## Abstract Deletion of the tumor suppressor gene p53 has been shown to improve the outcome in experimental models of focal cerebral ischemia and kainate‐induced seizures. To evaluate the potential role of p53 in traumatic brain injury, genetically modified mice lacking a functional p53 gene (p53^–

Frequent 3p allele loss and epigenetic i

Frequent 3p allele loss and epigenetic inactivation of the RASSF1A tumour suppressor gene from region 3p21.3 in head and neck squamous cell carcinoma

✍ R.P Hogg; S Honorio; A Martinez; A Agathanggelou; A Dallol; P Fullwood; R Weichs 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 349 KB

Frequent clonal loss of heterozygosity (

Frequent clonal loss of heterozygosity (LOH) in the chromosomal region 1p32 occurs in childhood T cell acute lymphoblastic leukemia (T-ALL) carrying rearrangements of the TAL1 gene

✍ Iolascon, A; Faienza, M F; Coppola, B; Moretti, A; Basso, G; Amaru, R; Viganò, G 📂 Article 📅 1997 🏛 Nature Publishing Group 🌐 English ⚖ 85 KB

Editorial comment on ‘Frequent 3p allele

Editorial comment on ‘Frequent 3p allele loss and epigenetic inactivation of the RASSF1A tumour suppressor gene from region 3p21.3 in head and neck squamous cell carcinoma’ by Hogg and colleagues

✍ M.W.M van den Brekel; A.J.M Balm 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 90 KB