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GGTI 298
Known as:
GGTI-298
National Institutes of Health
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Related topics
1 relation
Broader (1)
Benzamides
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Cross-talk between autophagy and KLF2 determines endothelial cell phenotype and microvascular function in acute liver injury.
Sergi Guixé-Muntet
,
F. C. de Mesquita
,
+5 authors
J. Gracia‐Sancho
Journal of Hepatology
2017
Corpus ID: 3427137
2007
2007
Adrenaline increases glucose transport via a Rap1‐p38MAPK pathway in rat vascular smooth muscle cells
Y. Kanda
,
Y. Watanabe
British Journal of Pharmacology
2007
Corpus ID: 27366815
Adrenaline has been implicated in the pathogenesis of atherosclerosis. However, little is known regarding the role of adrenaline…
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Highly Cited
2005
Highly Cited
2005
Statins Exert Endothelial Atheroprotective Effects via the KLF2 Transcription Factor*
K. Parmar
,
V. Nambudiri
,
G. Dai
,
H. B. Larman
,
M. Gimbrone
,
G. Garcı́a-Cardeña
Journal of Biological Chemistry
2005
Corpus ID: 23297226
3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, statins, have been shown to positively impact vascular function…
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Highly Cited
2002
Highly Cited
2002
Statin enhances cytokine-mediated induction of nitric oxide synthesis in vascular smooth muscle cells.
Y. Hattori
,
N. Nakanishi
,
K. Kasai
Cardiovascular Research
2002
Corpus ID: 25770698
Highly Cited
2001
Highly Cited
2001
Nitrogen-bisphosphonates block retinoblastoma phosphorylation and cell growth by inhibiting the cholesterol biosynthetic pathway in a keratinocyte model for esophageal irritation.
A. Reszka
,
J. Halasy-Nagy
,
G. Rodan
Molecular Pharmacology
2001
Corpus ID: 23285956
The surprising discovery that nitrogen-containing bisphosphonates (N-BPs) act via inhibition of the mevalonate-to-cholesterol…
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Highly Cited
2000
Highly Cited
2000
Protein Geranylgeranylation Is Required for Osteoclast Formation, Function, and Survival: Inhibition by Bisphosphonates and GGTI‐298
F. Coxon
,
M. Helfrich
,
+4 authors
M. Rogers
Journal of Bone and Mineral Research
2000
Corpus ID: 23634796
Bisphosphonates are the important class of antiresorptive drugs used in the treatment of metabolic bone diseases. Although their…
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Highly Cited
1998
Highly Cited
1998
p21WAF1/CIP1 Is Upregulated by the Geranylgeranyltransferase I Inhibitor GGTI-298 through a Transforming Growth Factor β- and Sp1-Responsive Element: Involvement of the Small GTPase RhoA
J. Adnane
,
Francisco A. Bizouarn
,
Y. Qian
,
A. Hamilton
,
S. Sebti
Molecular and Cellular Biology
1998
Corpus ID: 8713377
ABSTRACT We have recently reported that the geranylgeranyltransferase I inhibitor GGTI-298 arrests human tumor cells at the…
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Highly Cited
1997
Highly Cited
1997
GGTI-298 induces G0-G1 block and apoptosis whereas FTI-277 causes G2-M enrichment in A549 cells.
K. Miquel
,
A. Pradines
,
+4 authors
G. Favre
Cancer Research
1997
Corpus ID: 15929825
The mechanism by which the geranylgeranyltransferase I inhibitor GGTI-298 and the farnesyltransferase inhibitor FTI-277 inhibit…
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Highly Cited
1996
Highly Cited
1996
Protein geranylgeranylation, not farnesylation, is required for the G1 to S phase transition in mouse fibroblasts.
Andreas Vogt
,
Yimin Qian
,
Terence F. McGuire
,
Andrew D. Hamilton
,
Saíd M. Sebti
,
Saíd M. Sebti
Oncogene
1996
Corpus ID: 34046116
In order to assess the relative contributions of farnesylated and/or geranylgeranylated proteins on cell cycle progression from…
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Highly Cited
1996
Highly Cited
1996
Platelet-derived Growth Factor Receptor Tyrosine Phosphorylation Requires Protein Geranylgeranylation but not Farnesylation*
T. Mcguire
,
Y. Qian
,
A. Vogt
,
A. Hamilton
,
S. Sebti
Journal of Biological Chemistry
1996
Corpus ID: 11734154
We have used specific inhibitors for farnesyltransferase (FTase) and geranylgeranyltransferase (GGTase) I as well as combinations…
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