Article
Reduced growth of Drosophila neurofibromatosis 1 mutants reflects a non-cell-autonomous requirement for GTPase-Activating Protein activity in larval neurons.
Genes & development - 1 Dec 2006
Walker James A, Tchoudakova Anna V, McKenney Peter T, Brill Suzanne, Wu Dongyun, Cowley Glenn S, Hariharan Iswar K, Bernards André
Abstract excerpt
Neurofibromatosis type 1 (NF1) is among the most common genetic disorders of humans and is caused by loss of neurofibromin, a large and highly conserved protein whose only known function is to serve as a GTPase-Activating Protein (GAP) for Ras. However, most Drosophila NF1 mutant phenotypes, including an overall growth deficiency, are not readily modified by manipulating Ras signaling strength, but are rescued by...
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