๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The von Hippel-Lindau tumor suppressor gene protects cells from UV-mediated apoptosis

โœ Scribed by Schoenfeld, Alan R; Parris, Tchaiko; Eisenberger, Andrew; Davidowitz, Eliot J; Leon, Maryely De; Talasazan, Faranaz; Devarajan, Prasad; Burk, Robert D


Book ID
110064297
Publisher
Nature Publishing Group
Year
2000
Tongue
English
Weight
272 KB
Volume
19
Category
Article
ISSN
0950-9232

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Improved detection of germline mutations
โœ Catherine Stolle; Gladys Glenn; Berton Zbar; Jeffrey S. Humphrey; Peter Choyke; ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 201 KB ๐Ÿ‘ 2 views

Communicated by Victor A. McKusick von Hippel-Lindau disease (VHL) is an inherited neoplastic disorder characterized by the development of tumors in the eyes, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis. The VHL tumor suppressor gene was identified in 1993. Initial

The von Hippel-Lindau tumor suppressor g
โœ Jasmien Hoebeeck; Jo Vandesompele; Helรฉn Nilsson; Katleen De Preter; Nadine Van ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 166 KB

## Abstract Deletions of the short arm of chromosome 3 are often observed in a specific subset of aggressive neuroblastomas (NBs) with loss of distal 11q and without __MYCN__ amplification. The critical deleted region encompasses the locus of the von Hippelโ€Lindau gene (__VHL__, 3p25). Constitution