Ras farnesylation as a target for novel antitumor agents: Potent and selective farnesyl diphosphate analog inhibitors of farnesyltransferase-Reference-Cited by-同舟云学术

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Ras farnesylation as a target for novel antitumor agents: Potent and selective farnesyl diphosphate analog inhibitors of farnesyltransferase

Published:1995-02 Issue:2 Volume:34 Page:121-137
ISSN:0272-4391
Container-title:Drug Development Research
language:en
Short-container-title:Drug Dev. Res.

Author:

Manne Veeraswamy,Ricca Carolyn S.,Brown Johnni Gullo,Tuomari Anne V.,Yan Ning,Patel Dinesh,Schmidt Robert,Lynch Mark J.,Ciosek Carl P.,Carboni Joan M.,Robinson Simon,Gordon Eric M.,Barbacid Mariano,Seizinger Bernd R.,Biller Scott A.

Publisher

Wiley

Subject

Drug Discovery

Reference87 articles.

1. Endoproteolytic processing of a farnesylated peptide in vitro.

2. Isolation and DNA sequence of the STE14 gene encoding farnesyl cysteine: Carboxyl methyltransferase

3. ras GENES

4. The synthesis of isoprenoid (phosphinylmethyl)phosphonates

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