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Association of EXT1 and EXT2, Hereditary Multiple Exostoses Gene Products, in Golgi Apparatus

โœ Scribed by Shin-ichiro Kobayashi; Ko-ichi Morimoto; Takahiko Shimizu; Mayumi Takahashi; Hisashi Kurosawa; Takuji Shirasawa


Book ID
115585310
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
409 KB
Volume
268
Category
Article
ISSN
0006-291X

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๐Ÿ“œ SIMILAR VOLUMES


Molecular basis of multiple exostoses: m
โœ Wim Wuyts; Wim Van Hul ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 232 KB ๐Ÿ‘ 3 views

Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by the formation of exostoses, which are cartilage-capped bony protuberances mainly located on long bones. Two genes, EXT1 and EXT2, and at least one other unidentified gene, are known to be involved in the formation

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โœ Wendy H. Raskind; Ernest U. Conrad III; Mark Matsushita; Ellen M. Wijsman; Dan E ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 222 KB ๐Ÿ‘ 3 views

Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by growth of benign bone tumors. Three chromosomal loci have been implicated in this genetically heterogeneous disease: EXT1 at 8q24, EXT2 at 11p13, and EXT3 on 19p. EXT1 and EXT2 were recently cloned. We evaluated 3