-
1
-
-
0032401757
-
All in the family? New insights and questions regarding interconnectivity of Ras, Rap1 and Ral
-
BOS JL: All in the family? New insights and questions regarding interconnectivity of Ras, Rap1 and Ral. EMBO J. (1998) 17(23):6776-6782.
-
(1998)
EMBO J
, vol.17
, Issue.23
, pp. 6776-6782
-
-
BOS, J.L.1
-
2
-
-
0032541650
-
Increasing complexity of Ras signaling
-
Oncogene
-
CAMPBELL SL, KHOSRAVI-FAR R, ROSSMAN KL, CLARK GJ, DER CJ: Increasing complexity of Ras signaling. Oncogene (1998) 17(11 Reviews):1395-1413.
-
(1998)
11 Reviews
, vol.17
, pp. 1395-1413
-
-
CAMPBELL, S.L.1
KHOSRAVI-FAR, R.2
ROSSMAN, K.L.3
CLARK, G.J.4
DER, C.J.5
-
3
-
-
0024410291
-
Structural and functional properties of ras proteins
-
SANTOS E, NEBREDA AR: Structural and functional properties of ras proteins. FASEB J. (1989) 3(10):2151-2163.
-
(1989)
FASEB J
, vol.3
, Issue.10
, pp. 2151-2163
-
-
SANTOS, E.1
NEBREDA, A.R.2
-
4
-
-
0033538559
-
Endomembrane trafficking of ras: The CAAX motif targets proteins to the ER and Golgi
-
CHOY E, CHIU VK, SILLETTI J et al.: Endomembrane trafficking of ras: the CAAX motif targets proteins to the ER and Golgi. Cell (1999) 98(1):69-80.
-
(1999)
Cell
, vol.98
, Issue.1
, pp. 69-80
-
-
CHOY, E.1
CHIU, V.K.2
SILLETTI, J.3
-
5
-
-
0025120211
-
Regulation of the mevalonate pathway
-
GOLDSTEIN JL, BROWN MS: Regulation of the mevalonate pathway. Nature (1990) 343(6257):425-430.
-
(1990)
Nature
, vol.343
, Issue.6257
, pp. 425-430
-
-
GOLDSTEIN, J.L.1
BROWN, M.S.2
-
6
-
-
0034104590
-
The Ras branch of small GTPases: Ras family members don't fall far from the tree
-
REUTHER GW, DER CJ: The Ras branch of small GTPases: Ras family members don't fall far from the tree. Curr. Opin. Cell Biol. (2000) 12(2):157-165.
-
(2000)
Curr. Opin. Cell Biol
, vol.12
, Issue.2
, pp. 157-165
-
-
REUTHER, G.W.1
DER, C.J.2
-
7
-
-
0026072339
-
Enzymatic modification of proteins with a geranylgeranyl isoprenoid
-
CASEY PJ, THISSEN JA, MOOMAW JF: Enzymatic modification of proteins with a geranylgeranyl isoprenoid. Proc. Natl. Acad. Sci. USA (1991) 88(19):8631-8635.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, Issue.19
, pp. 8631-8635
-
-
CASEY, P.J.1
THISSEN, J.A.2
MOOMAW, J.F.3
-
8
-
-
0026001936
-
A protein geranylgeranyltransferase from bovine brain: Implications for protein prenylation specificity
-
YOKOYAMA K, GOODWIN GW, GHOMASHCHI F, GLOMSET JA, GELB MH: A protein geranylgeranyltransferase from bovine brain: implications for protein prenylation specificity. Proc. Natl. Acad. Sci. USA (1991) 88(12):5302-5306.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, Issue.12
, pp. 5302-5306
-
-
YOKOYAMA, K.1
GOODWIN, G.W.2
GHOMASHCHI, F.3
GLOMSET, J.A.4
GELB, M.H.5
-
9
-
-
0026735063
-
Protein isoprenylation and methylation at carboxyl-terminal cysteine residues
-
CLARKE S: Protein isoprenylation and methylation at carboxyl-terminal cysteine residues. Annu. Rev. Biochem. (1992) 61:355-386.
-
(1992)
Annu. Rev. Biochem
, vol.61
, pp. 355-386
-
-
CLARKE, S.1
-
10
-
-
0029898894
-
Protein prenylation: Molecular mechanisms and functional consequences
-
ZHANG FL, CASEY PJ: Protein prenylation: molecular mechanisms and functional consequences. Annu. Rev. Biochem. (1996) 65:241-269.
-
(1996)
Annu. Rev. Biochem
, vol.65
, pp. 241-269
-
-
ZHANG, F.L.1
CASEY, P.J.2
-
11
-
-
0026021456
-
Methylation and proteolysis are essential for efficient membrane binding of prenylated p21K-ras(B)
-
HANCOCK JF, CADWALLADER K, MARSHALL CJ: Methylation and proteolysis are essential for efficient membrane binding of prenylated p21K-ras(B). EMBO J. (1991) 10(3):641-646.
-
(1991)
EMBO J
, vol.10
, Issue.3
, pp. 641-646
-
-
HANCOCK, J.F.1
CADWALLADER, K.2
MARSHALL, C.J.3
-
12
-
-
0000081175
-
Posttranslational modification of the Ha-ras oncogene protein: Evidence for a third class of protein carboxyl methyltransferases
-
CLARKE S, VOGEL JP, DESCHENES RJ, STOCK J: Posttranslational modification of the Ha-ras oncogene protein: evidence for a third class of protein carboxyl methyltransferases. Proc. Natl. Acad. Sci. USA (1988) 85(13):4643-4647.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, Issue.13
, pp. 4643-4647
-
-
CLARKE, S.1
VOGEL, J.P.2
DESCHENES, R.J.3
STOCK, J.4
-
13
-
-
0027153103
-
Epidermal growth factor regulates p21ras through the formation of a complex of receptor, Grb2 adapter protein, and Sos nucleotide exchange factor
-
BUDAY L, DOWNWARD J: Epidermal growth factor regulates p21ras through the formation of a complex of receptor, Grb2 adapter protein, and Sos nucleotide exchange factor. Cell (1993) 73(3):611-620.
-
(1993)
Cell
, vol.73
, Issue.3
, pp. 611-620
-
-
BUDAY, L.1
DOWNWARD, J.2
-
14
-
-
0028694342
-
Activation of Ras by receptor tyrosine kinases
-
MARGOLIS B, SKOLNIK EY: Activation of Ras by receptor tyrosine kinases. J. Am. Soc. Nephrol. (1994) 5(6): 1288-1299.
-
(1994)
J. Am. Soc. Nephrol
, vol.5
, Issue.6
, pp. 1288-1299
-
-
MARGOLIS, B.1
SKOLNIK, E.Y.2
-
16
-
-
0035829731
-
Galectin-1 binds oncogenic H-Ras to mediate Ras membrane anchorage and cell transformation
-
PAZ A, HAKLAI R, ELAD-SFADIA G, BALLAN E, KLOOG Y: Galectin-1 binds oncogenic H-Ras to mediate Ras membrane anchorage and cell transformation. Oncogene (2001) 20(51):7486-7493.
-
(2001)
Oncogene
, vol.20
, Issue.51
, pp. 7486-7493
-
-
PAZ, A.1
HAKLAI, R.2
ELAD-SFADIA, G.3
BALLAN, E.4
KLOOG, Y.5
-
17
-
-
4544295231
-
Galectin-3 augments K-Ras activation and triggers a Ras signal that attenuates ERK but not phosphoinositide 3-kinase activity
-
ELAD-SFADIA G, HAKLAI R, BALAN E, KLOOG Y: Galectin-3 augments K-Ras activation and triggers a Ras signal that attenuates ERK but not phosphoinositide 3-kinase activity. J. Biol. Chem. (2004) 279(33):34922-34930.
-
(2004)
J. Biol. Chem
, vol.279
, Issue.33
, pp. 34922-34930
-
-
ELAD-SFADIA, G.1
HAKLAI, R.2
BALAN, E.3
KLOOG, Y.4
-
18
-
-
0037020243
-
Galectin-1 augments Ras activation and diverts Ras signals to Raf-1 at the expense of phosphoinositide 3-kinase
-
ELAD-SFADIA G, HAKLAI R, BALLAN E, GABIUS HJ, KLOOG Y: Galectin-1 augments Ras activation and diverts Ras signals to Raf-1 at the expense of phosphoinositide 3-kinase. J. Biol. Chem. (2002) 277(40):37169- 37175.
-
(2002)
J. Biol. Chem
, vol.277
, Issue.40
, pp. 37169-37175
-
-
ELAD-SFADIA, G.1
HAKLAI, R.2
BALLAN, E.3
GABIUS, H.J.4
KLOOG, Y.5
-
19
-
-
0034175984
-
Understanding Ras: 'it ain't over 'til it's over'
-
SHIELDS JM, PRUITT K, MCFALL A, SHAUB A, DER CJ: Understanding Ras: 'it ain't over 'til it's over'. Trends Cell Biol. (2000) 10(4):147- 154.
-
(2000)
Trends Cell Biol
, vol.10
, Issue.4
, pp. 147-154
-
-
SHIELDS, J.M.1
PRUITT, K.2
MCFALL, A.3
SHAUB, A.4
DER, C.J.5
-
20
-
-
0025979335
-
Raf-1 protein kinase is required for growth of induced NIH/3T3 cells
-
KOLCH W, HEIDECKER G, LLOYD P, RAPP UR: Raf-1 protein kinase is required for growth of induced NIH/3T3 cells. Nature (1991) 349(6308):426- 428.
-
(1991)
Nature
, vol.349
, Issue.6308
, pp. 426-428
-
-
KOLCH, W.1
HEIDECKER, G.2
LLOYD, P.3
RAPP, U.R.4
-
21
-
-
0027161398
-
Complex formation between RAS and RAF and other protein kinases
-
VAN AELST L, BARR M, MARCUS S, POLVERINO A, WIGLER M: Complex formation between RAS and RAF and other protein kinases. Proc. Natl. Acad. Sci. USA (1993) 90(13):6213-6217.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, Issue.13
, pp. 6213-6217
-
-
VAN AELST, L.1
BARR, M.2
MARCUS, S.3
POLVERINO, A.4
WIGLER, M.5
-
22
-
-
12144286410
-
Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis
-
LOH ML, VATTIKUTI S, SCHUBBERT S et al.: Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis. Blood (2004) 103(6):2325-2331.
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2325-2331
-
-
LOH, M.L.1
VATTIKUTI, S.2
SCHUBBERT, S.3
-
23
-
-
0028272507
-
Requirement for Ras in Raf activation is overcome by targeting Raf to the plasma membrane
-
LEEVERS SJ, PATERSON HF, MARSHALL CJ: Requirement for Ras in Raf activation is overcome by targeting Raf to the plasma membrane. Nature (1994) 369(6479):411-414.
-
(1994)
Nature
, vol.369
, Issue.6479
, pp. 411-414
-
-
LEEVERS, S.J.1
PATERSON, H.F.2
MARSHALL, C.J.3
-
25
-
-
0031900740
-
Signal transduction through MAP kinase cascades
-
LEWIS TS, SHAPIRO PS, AHN NG: Signal transduction through MAP kinase cascades. Adv. Cancer Res. (1998) 74:49-139.
-
(1998)
Adv. Cancer Res
, vol.74
, pp. 49-139
-
-
LEWIS, T.S.1
SHAPIRO, P.S.2
AHN, N.G.3
-
26
-
-
0027425113
-
Activation of ternary complex factor Elk-1 by MAP kinases
-
JANKNECHT R, ERNST WH, PINGOUD V, NORDHEIM A: Activation of ternary complex factor Elk-1 by MAP kinases. EMBO J. (1993) 12(13):5097- 5104.
-
(1993)
EMBO J
, vol.12
, Issue.13
, pp. 5097-5104
-
-
JANKNECHT, R.1
ERNST, W.H.2
PINGOUD, V.3
NORDHEIM, A.4
-
27
-
-
0035908493
-
Blocking oncogenic Ras signaling for cancer therapy
-
ADJEI AA: Blocking oncogenic Ras signaling for cancer therapy. J. Natl. Cancer Inst. (2001) 93(14):1062-1074.
-
(2001)
J. Natl. Cancer Inst
, vol.93
, Issue.14
, pp. 1062-1074
-
-
ADJEI, A.A.1
-
28
-
-
0032541671
-
Cell cycle targets of Ras/Raf signalling
-
Oncogene
-
KERKHOFF E, RAPP UR: Cell cycle targets of Ras/Raf signalling. Oncogene (1998) 17(11 Reviews):1457-1462.
-
(1998)
11 Reviews
, vol.17
, pp. 1457-1462
-
-
KERKHOFF, E.1
RAPP, U.R.2
-
30
-
-
0029990003
-
Activation of phosphoinositide 3-kinase by interaction with Ras and by point mutation
-
RODRIGUEZ-VICIANA P, WARNE PH, VANHAESEBROECK B, WATERFIELD MD, DOWNWARD J: Activation of phosphoinositide 3-kinase by interaction with Ras and by point mutation. EMBO. J. (1996) 15(10):2442-2451.
-
(1996)
EMBO. J
, vol.15
, Issue.10
, pp. 2442-2451
-
-
RODRIGUEZ-VICIANA, P.1
WARNE, P.H.2
VANHAESEBROECK, B.3
WATERFIELD, M.D.4
DOWNWARD, J.5
-
31
-
-
0037264633
-
Targeting RAS signalling pathways in cancer therapy
-
DOWNWARD J: Targeting RAS signalling pathways in cancer therapy. Nat. Rev. Cancer (2003) 3(1):11-22.
-
(2003)
Nat. Rev. Cancer
, vol.3
, Issue.1
, pp. 11-22
-
-
DOWNWARD, J.1
-
32
-
-
0037394676
-
Neutrophils and acute lung injury
-
ABRAHAM E: Neutrophils and acute lung injury. Crit. Care Med. (2003) 31(4 Suppl.):S195-S199.
-
(2003)
Crit. Care Med
, vol.31
, Issue.4 SUPPL.
-
-
ABRAHAM, E.1
-
33
-
-
0030702123
-
Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery
-
DATTA SR, DUDEK H, TAO X et al.: Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery. Cell (1997) 91(2):231-241.
-
(1997)
Cell
, vol.91
, Issue.2
, pp. 231-241
-
-
DATTA, S.R.1
DUDEK, H.2
TAO, X.3
-
34
-
-
0032515027
-
Regulation of cell deadi protease caspase-9 by phosphorylation
-
CARDONE MH, ROY N, STENNICKE HR et al.: Regulation of cell deadi protease caspase-9 by phosphorylation. Science (1998) 282(5392):1318-1321.
-
(1998)
Science
, vol.282
, Issue.5392
, pp. 1318-1321
-
-
CARDONE, M.H.1
ROY, N.2
STENNICKE, H.R.3
-
35
-
-
0036723650
-
MLL-AFX requires the transcriptional effector domains of AFX to transform myeloid progenitors and transdominamly interfere with forkhead protein function
-
SO CW, CLEARY ML: MLL-AFX requires the transcriptional effector domains of AFX to transform myeloid progenitors and transdominamly interfere with forkhead protein function. Mol. Cell Biol. (2002) 22(18):6542- 6552.
-
(2002)
Mol. Cell Biol
, vol.22
, Issue.18
, pp. 6542-6552
-
-
SO, C.W.1
CLEARY, M.L.2
-
36
-
-
33645791232
-
Coordination of NF-kappaB and NFAT antagonism by the forkhead transcription factor Foxd1
-
LIN L, PENG SL: Coordination of NF-kappaB and NFAT antagonism by the forkhead transcription factor Foxd1. J. Immunol. (2006) 176(8):4793-4803.
-
(2006)
J. Immunol
, vol.176
, Issue.8
, pp. 4793-4803
-
-
LIN, L.1
PENG, S.L.2
-
37
-
-
33746016268
-
Mitochondria: More than just a powerhouse
-
MCBRIDE HM, NEUSPIEL M, WASIAK S: Mitochondria: more than just a powerhouse. Curr. Biol. (2006) 16(14):551-560.
-
(2006)
Curr. Biol
, vol.16
, Issue.14
, pp. 551-560
-
-
MCBRIDE, H.M.1
NEUSPIEL, M.2
WASIAK, S.3
-
38
-
-
0033517189
-
NF-kappaB activation by tumour necrosis factor requires the Akt serine-threonine kinase
-
OZES ON, MAYO LD, GUSTIN JA, PFEFFER SR, PFEFFER LM, DONNER DB: NF-kappaB activation by tumour necrosis factor requires the Akt serine-threonine kinase. Nature (1999) 401(6748):82-85.
-
(1999)
Nature
, vol.401
, Issue.6748
, pp. 82-85
-
-
OZES, O.N.1
MAYO, L.D.2
GUSTIN, J.A.3
PFEFFER, S.R.4
PFEFFER, L.M.5
DONNER, D.B.6
-
39
-
-
0028903247
-
An essential role for Rac in Ras transformation
-
QIU RG, CHEN J, KIRN D, MCCORMICK F, SYMONS M: An essential role for Rac in Ras transformation. Nature (1995) 374(6521):457-459.
-
(1995)
Nature
, vol.374
, Issue.6521
, pp. 457-459
-
-
QIU, R.G.1
CHEN, J.2
KIRN, D.3
MCCORMICK, F.4
SYMONS, M.5
-
40
-
-
0842304369
-
Mammalian target of rapamycin inhibition as therapy for hematologic malignancies
-
PANWALKAR A, VERSTOVSEK S, GILES FJ: Mammalian target of rapamycin inhibition as therapy for hematologic malignancies. Cancer (2004) 100(4):657-666.
-
(2004)
Cancer
, vol.100
, Issue.4
, pp. 657-666
-
-
PANWALKAR, A.1
VERSTOVSEK, S.2
GILES, F.J.3
-
41
-
-
0033029811
-
Ras caught in another affair: The exchange factors for Ral
-
WOLTHUIS RM, BOS JL: Ras caught in another affair: the exchange factors for Ral. Curr. Opin. Genet. Dev. (1999) 9(1):112-117.
-
(1999)
Curr. Opin. Genet. Dev
, vol.9
, Issue.1
, pp. 112-117
-
-
WOLTHUIS, R.M.1
BOS, J.L.2
-
42
-
-
16644370412
-
Human RAS superfamily proteins and related GTPases
-
COLICELLI J: Human RAS superfamily proteins and related GTPases. Sci. STKE (2004) 2004(250):RE13.
-
(2004)
Sci. STKE
, vol.2004
, Issue.250
-
-
COLICELLI, J.1
-
43
-
-
0042353628
-
RAL GTPases are linchpin modulators of human tumour-cell proliferation and survival
-
800-806
-
CHIEN Y, WHITE MA: RAL GTPases are linchpin modulators of human tumour-cell proliferation and survival. EMBO Rep. (2003) 4(8):800-806.
-
(2003)
EMBO Rep
, vol.4
, Issue.8
-
-
CHIEN, Y.1
WHITE, M.A.2
-
44
-
-
2342418629
-
Rho-family GTPases: It's not only Rac and Rho (and I like it)
-
WENNERBERG K, DER CJ: Rho-family GTPases: it's not only Rac and Rho (and I like it). J. Cell Sci. (2004) 117(Pt 8):1301-1312.
-
(2004)
J. Cell Sci
, vol.117
, Issue.PART 8
, pp. 1301-1312
-
-
WENNERBERG, K.1
DER, C.J.2
-
45
-
-
0035839569
-
The brain exocyst complex interacts with RalA in a GTP-dependent manner: Identification of a novel mammalian Sec3 gene and a second Sec15 gene
-
BRYMORA A, VALOVA VA, LARSEN MR, ROUFOGALIS BD, ROBINSON PJ: The brain exocyst complex interacts with RalA in a GTP-dependent manner: identification of a novel mammalian Sec3 gene and a second Sec15 gene. J. Biol. Chem. (2001) 276(32):29792-29797.
-
(2001)
J. Biol. Chem
, vol.276
, Issue.32
, pp. 29792-29797
-
-
BRYMORA, A.1
VALOVA, V.A.2
LARSEN, M.R.3
ROUFOGALIS, B.D.4
ROBINSON, P.J.5
-
46
-
-
13244260780
-
RalA interacts with ZONAB in a cell density-dependent manner and regulates its transcriptional activity
-
FRANKEL P, ARONHEIM A, KAVANAGH E et al.: RalA interacts with ZONAB in a cell density-dependent manner and regulates its transcriptional activity. EMBO J. (2005) 24(1):54-62.
-
(2005)
EMBO J
, vol.24
, Issue.1
, pp. 54-62
-
-
FRANKEL, P.1
ARONHEIM, A.2
KAVANAGH, E.3
-
47
-
-
20444477143
-
Regulation of phospholipase C-delta1 through direct interactions with the small GTPase Ral and calmodulin
-
SIDHU RS, CLOUGH RR, BHULLAR RP: Regulation of phospholipase C-delta1 through direct interactions with the small GTPase Ral and calmodulin. J. Biol. Chem. (2005) 280(23):21933-21941.
-
(2005)
J. Biol. Chem
, vol.280
, Issue.23
, pp. 21933-21941
-
-
SIDHU, R.S.1
CLOUGH, R.R.2
BHULLAR, R.P.3
-
49
-
-
23644455714
-
Phospholipase D: A lipid centric review
-
JENKINS GM, FROHMAN MA: Phospholipase D: a lipid centric review. Cell Mol. Life Sci. (2005) 62(19-20):2305-2316.
-
(2005)
Cell Mol. Life Sci
, vol.62
, Issue.19-20
, pp. 2305-2316
-
-
JENKINS, G.M.1
FROHMAN, M.A.2
-
50
-
-
0033014304
-
RAS and leukemia: From basic mechanisms to gene-directed therapy
-
BEAUPRE DM, KURZROCK R: RAS and leukemia: from basic mechanisms to gene-directed therapy. J. Clin. Oncol. (1999) 17(3):1071-1079.
-
(1999)
J. Clin. Oncol
, vol.17
, Issue.3
, pp. 1071-1079
-
-
BEAUPRE, D.M.1
KURZROCK, R.2
-
51
-
-
0024376173
-
Ras oncogenes in human cancer: A review
-
BOS JL: Ras oncogenes in human cancer: a review. Cancer Res. (1989) 49(17):4682-4689.
-
(1989)
Cancer Res
, vol.49
, Issue.17
, pp. 4682-4689
-
-
BOS, J.L.1
-
52
-
-
0024292722
-
Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes
-
ALMOGUERA C, SHIBATA D, FORRESTER K, MARTIN J, ARNHEIM N, PERUCHO M: Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes. Cell (1988) 53(4):549-554.
-
(1988)
Cell
, vol.53
, Issue.4
, pp. 549-554
-
-
ALMOGUERA, C.1
SHIBATA, D.2
FORRESTER, K.3
MARTIN, J.4
ARNHEIM, N.5
PERUCHO, M.6
-
53
-
-
0026909770
-
Ras and human tumors
-
RODENHUIS S: Ras and human tumors. Semin. Cancer Biol. (1992) 3(4):241-247.
-
(1992)
Semin. Cancer Biol
, vol.3
, Issue.4
, pp. 241-247
-
-
RODENHUIS, S.1
-
54
-
-
24744449132
-
RAS mutation in acute myeloid leukemia is associated with distinct cytogenetic subgroups but does not influence outcome in patients younger than 60 years
-
BOWEN DT, FREW ME, HILLS R et al.: RAS mutation in acute myeloid leukemia is associated with distinct cytogenetic subgroups but does not influence outcome in patients younger than 60 years. Blood (2005) 106(6):2113-2119.
-
(2005)
Blood
, vol.106
, Issue.6
, pp. 2113-2119
-
-
BOWEN, D.T.1
FREW, M.E.2
HILLS, R.3
-
55
-
-
33646575624
-
Implications of NRAS mutations in AML: A study of 2502 patients
-
BACHER U, HAFERLACH T, SCHOCH C, KERN W, SCHNITTGER S: Implications of NRAS mutations in AML: a study of 2502 patients. Blood (2006) 107(10):3847-3853.
-
(2006)
Blood
, vol.107
, Issue.10
, pp. 3847-3853
-
-
BACHER, U.1
HAFERLACH, T.2
SCHOCH, C.3
KERN, W.4
SCHNITTGER, S.5
-
56
-
-
9144253166
-
Prognostic significance of N-RAS and K-RAS mutations in 232 patients with acute myeloid leukemia
-
RITTER M, KIM TD, LISSKE P, THIEDE C, SCHAICH M, NEUBAUER A: Prognostic significance of N-RAS and K-RAS mutations in 232 patients with acute myeloid leukemia. Haematologica (2004) 89(11):1397-1399.
-
(2004)
Haematologica
, vol.89
, Issue.11
, pp. 1397-1399
-
-
RITTER, M.1
KIM, T.D.2
LISSKE, P.3
THIEDE, C.4
SCHAICH, M.5
NEUBAUER, A.6
-
57
-
-
33744496772
-
Acquisition of JAK2, PTPN11, and RAS mutations during disease progression in primary myelodysplastic syndrome
-
CHEN CY, LIN LI, TANG JL et al.: Acquisition of JAK2, PTPN11, and RAS mutations during disease progression in primary myelodysplastic syndrome. Leukemia (2006) 20(6):1155-1158.
-
(2006)
Leukemia
, vol.20
, Issue.6
, pp. 1155-1158
-
-
CHEN, C.Y.1
LIN, L.I.2
TANG, J.L.3
-
58
-
-
17344371122
-
RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: A 10-year follow-up
-
PADUA RA, GUINN BA, AL-SABAH AI et al.: RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: a 10-year follow-up. Leukemia (1998) 12(6):887-892.
-
(1998)
Leukemia
, vol.12
, Issue.6
, pp. 887-892
-
-
PADUA, R.A.1
GUINN, B.A.2
AL-SABAH, A.I.3
-
59
-
-
0032007206
-
Correlation of N-ras point mutations with specific chromosomal abnormalities in primary myelodysplastic syndrome
-
DE SOUZA FERNANDEZ T, MENEZES DE SOUZA J, MACEDO SILVA ML, TABAK D, ABDELHAY E: Correlation of N-ras point mutations with specific chromosomal abnormalities in primary myelodysplastic syndrome. Leuk. Res. (1998) 22(2):125-134.
-
(1998)
Leuk. Res
, vol.22
, Issue.2
, pp. 125-134
-
-
DE SOUZA FERNANDEZ, T.1
MENEZES DE SOUZA, J.2
MACEDO SILVA ML, T.D.3
ABDELHAY, E.4
-
60
-
-
0024380306
-
Mechanisms of ras mutation in myelodysplastic syndrome
-
YUNIS JJ, BOOT AJ, MAYER MG, BOS JL: Mechanisms of ras mutation in myelodysplastic syndrome. Oncogene (1989) 4(5):609-614.
-
(1989)
Oncogene
, vol.4
, Issue.5
, pp. 609-614
-
-
YUNIS, J.J.1
BOOT, A.J.2
MAYER, M.G.3
BOS, J.L.4
-
61
-
-
0032704708
-
Ras protein farnesyltransferase: A strategic target for anticancer therapeutic development
-
ROWINSKY EK, WINDLE JJ, VON HOFF DD: Ras protein farnesyltransferase: a strategic target for anticancer therapeutic development. J. Clin. Oncol. (1999) 17(11):3631-3652.
-
(1999)
J. Clin. Oncol
, vol.17
, Issue.11
, pp. 3631-3652
-
-
ROWINSKY, E.K.1
WINDLE, J.J.2
VON HOFF, D.D.3
-
62
-
-
0028958919
-
Polylysine and CVIM sequences of K-RasB dictate specificity of prenylation and confer resistance to benzodiazepine peptidomimetic in vitro
-
JAMES GL, GOLDSTEIN JL, BROWN MS: Polylysine and CVIM sequences of K-RasB dictate specificity of prenylation and confer resistance to benzodiazepine peptidomimetic in vitro. J. Biol. Chem. (1995) 270(11):6221-6226.
-
(1995)
J. Biol. Chem
, vol.270
, Issue.11
, pp. 6221-6226
-
-
JAMES, G.L.1
GOLDSTEIN, J.L.2
BROWN, M.S.3
-
63
-
-
0035321186
-
RPR-115135, a new non peptidomimetic farnesyltransferase inhibitor, induces G0/G1 arrest only in serum starved cells
-
RUSSO P, OTTOBONI C, CRIPPA A, RIOU JF, O'CONNOR PM: RPR-115135, a new non peptidomimetic farnesyltransferase inhibitor, induces G0/G1 arrest only in serum starved cells. Int. J. Oncol. (2001) 18(4):855-862.
-
(2001)
Int. J. Oncol
, vol.18
, Issue.4
, pp. 855-862
-
-
RUSSO, P.1
OTTOBONI, C.2
CRIPPA, A.3
RIOU, J.F.4
O'CONNOR, P.M.5
-
64
-
-
0031820282
-
J-104,871, a novel farnesyltransferase inhibitor, blocks Ras farnesylation in vivo in a farnesyl pyrophosphate-competitive manner
-
YONEMOTO M, SATOH T, ARAKAWA H et al.: J-104,871, a novel farnesyltransferase inhibitor, blocks Ras farnesylation in vivo in a farnesyl pyrophosphate-competitive manner. Mol. Pharmacol. (1998) 54(1):1-7.
-
(1998)
Mol. Pharmacol
, vol.54
, Issue.1
, pp. 1-7
-
-
YONEMOTO, M.1
SATOH, T.2
ARAKAWA, H.3
-
65
-
-
0037143092
-
RPR-115135, a farnesyltransferase inhibitor, increases 5-FU-cytotoxicity in ten human colon cancer cell lines: Role of p53
-
RUSSO P, MALACARNE D, FALUGI C, TROMBINO S, O'CONNOR PM: RPR-115135, a farnesyltransferase inhibitor, increases 5-FU-cytotoxicity in ten human colon cancer cell lines: role of p53. Int. J. Cancer (2002) 100(3):266-275.
-
(2002)
Int. J. Cancer
, vol.100
, Issue.3
, pp. 266-275
-
-
RUSSO, P.1
MALACARNE, D.2
FALUGI, C.3
TROMBINO, S.4
O'CONNOR, P.M.5
-
66
-
-
0037379694
-
Increasing complexity of farnesyltransferase inhibitors activity: Role in chromosome instability
-
FALUGI C, TROMBINO S, GRANONE P, MARGARITORA S, RUSSO P: Increasing complexity of farnesyltransferase inhibitors activity: role in chromosome instability. Curr. Cancer Drug Targets (2003) 3(2):109-118.
-
(2003)
Curr. Cancer Drug Targets
, vol.3
, Issue.2
, pp. 109-118
-
-
FALUGI, C.1
TROMBINO, S.2
GRANONE, P.3
MARGARITORA, S.4
RUSSO, P.5
-
67
-
-
0035678051
-
-
BRITTEN CD, ROWINSKY EK, SOIGNET S et al.: A Phase I and pharmacological study of the farnesyl protein transferase inhibitor L-778,123 in patients with solid malignancies. Clin. Cancer Res. (2001) 7(12):3894-3903.
-
BRITTEN CD, ROWINSKY EK, SOIGNET S et al.: A Phase I and pharmacological study of the farnesyl protein transferase inhibitor L-778,123 in patients with solid malignancies. Clin. Cancer Res. (2001) 7(12):3894-3903.
-
-
-
-
68
-
-
4644362784
-
Farnesyltransferase inhibitors as anticancer agents: Critical crossroads
-
DOLL RJ, KIRSCHMEIER P, BISHOP WR: Farnesyltransferase inhibitors as anticancer agents: critical crossroads. Curr. Opin. Drug Discov. Devel. (2004) 7(4):478-486.
-
(2004)
Curr. Opin. Drug Discov. Devel
, vol.7
, Issue.4
, pp. 478-486
-
-
DOLL, R.J.1
KIRSCHMEIER, P.2
BISHOP, W.R.3
-
69
-
-
0029000897
-
Bisubstrate inhibitors of farnesyltransferase: A novel class of specific inhibitors of ras transformed cells
-
MANNE V, YAN N, CARBONI JM et al.: Bisubstrate inhibitors of farnesyltransferase: a novel class of specific inhibitors of ras transformed cells. Oncogene (1995) 10(9):1763-1779.
-
(1995)
Oncogene
, vol.10
, Issue.9
, pp. 1763-1779
-
-
MANNE, V.1
YAN, N.2
CARBONI, J.M.3
-
70
-
-
8644219632
-
Clinical activity of farnesyl transferase inhibitors in hematologic malignancies: Possible mechanisms of action
-
JABBOUR E, KANTARJIAN H, CORTES J: Clinical activity of farnesyl transferase inhibitors in hematologic malignancies: possible mechanisms of action. Leuk. Lymphoma (2004) 45(11):2187-2195.
-
(2004)
Leuk. Lymphoma
, vol.45
, Issue.11
, pp. 2187-2195
-
-
JABBOUR, E.1
KANTARJIAN, H.2
CORTES, J.3
-
71
-
-
14344254868
-
Antitumor activity of SCH 66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase, in human tumor xenograft models and wap-ras transgenic mice
-
LIU M, BRYANT MS, CHEN J et al.: Antitumor activity of SCH 66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase, in human tumor xenograft models and wap-ras transgenic mice. Cancer Res. (1998) 58(21):4947-4956.
-
(1998)
Cancer Res
, vol.58
, Issue.21
, pp. 4947-4956
-
-
LIU, M.1
BRYANT, M.S.2
CHEN, J.3
-
72
-
-
0036655361
-
Farnesyltransferase inhibitors: Novel compounds in development for the treatment of myeloid malignancies
-
CORTES JE, KURZROCK R, KANTARJIAN HM: Farnesyltransferase inhibitors: novel compounds in development for the treatment of myeloid malignancies. Semin. Hematol. (2002) 39(3 Suppl. 2):26-30.
-
(2002)
Semin. Hematol
, vol.39
, Issue.3 SUPPL. 2
, pp. 26-30
-
-
CORTES, J.E.1
KURZROCK, R.2
KANTARJIAN, H.M.3
-
73
-
-
0035132538
-
Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro
-
END DW, SMETS G, TODD AY et al.: Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro. Cancer Res. (2001) 61(1):131-137.
-
(2001)
Cancer Res
, vol.61
, Issue.1
, pp. 131-137
-
-
END, D.W.1
SMETS, G.2
TODD, A.Y.3
-
74
-
-
0034846550
-
Farnesyl protein transferase inhibitors as targeted therapies for hematologic malignancies
-
KARP JE: Farnesyl protein transferase inhibitors as targeted therapies for hematologic malignancies. Semin. Hematol. (2001) 38(3 Suppl. 7):16-23.
-
(2001)
Semin. Hematol
, vol.38
, Issue.3 SUPPL. 7
, pp. 16-23
-
-
KARP, J.E.1
-
75
-
-
0035383789
-
Clinical and biologic activity of the farnesyltransferase inhibitor R115777 in adults with refractory and relapsed acute leukemias: A Phase 1 clinical-laboratory correlative trial
-
KARP JE, LANCET JE, KAUFMANN SH et al.: Clinical and biologic activity of the farnesyltransferase inhibitor R115777 in adults with refractory and relapsed acute leukemias: a Phase 1 clinical-laboratory correlative trial. Blood (2001) 97(11):3361-3369.
-
(2001)
Blood
, vol.97
, Issue.11
, pp. 3361-3369
-
-
KARP, J.E.1
LANCET, J.E.2
KAUFMANN, S.H.3
-
76
-
-
0037699302
-
Farnesyl transferase inhibitors in myeloid malignancies
-
LANCET JE, KARP JE: Farnesyl transferase inhibitors in myeloid malignancies. Blood Rev. (2003) 17(3):123-129.
-
(2003)
Blood Rev
, vol.17
, Issue.3
, pp. 123-129
-
-
LANCET, J.E.1
KARP, J.E.2
-
77
-
-
0037372488
-
Efficacy of the farnesyl transferase inhibitor R115777 in chronic myeloid leukemia and other hematologic malignancies
-
CORTES J, ALBITAR M, THOMAS D et al.: Efficacy of the farnesyl transferase inhibitor R115777 in chronic myeloid leukemia and other hematologic malignancies. Blood (2003) 101(5):1692-1697.
-
(2003)
Blood
, vol.101
, Issue.5
, pp. 1692-1697
-
-
CORTES, J.1
ALBITAR, M.2
THOMAS, D.3
-
78
-
-
10744227474
-
Farnesyltransferase inhibitor R115777 in myelodysplastic syndrome: Clinical and biologic activities in the Phase 1 setting
-
KURZROCK R, KANTARJIAN HM, CORTES JE et al.: Farnesyltransferase inhibitor R115777 in myelodysplastic syndrome: clinical and biologic activities in the Phase 1 setting. Blood (2003) 102(13):4527-4534.
-
(2003)
Blood
, vol.102
, Issue.13
, pp. 4527-4534
-
-
KURZROCK, R.1
KANTARJIAN, H.M.2
CORTES, J.E.3
-
79
-
-
2142712474
-
Phase II study of R115777, a farnesyl transferase inhibitor, in myelodysplastic syndrome
-
KURZROCK R, ALBITAR M, CORTES JE et al.: Phase II study of R115777, a farnesyl transferase inhibitor, in myelodysplastic syndrome.in. Oncol. (2004) 22(7):1287-1292.
-
(2004)
Oncol
, vol.22
, Issue.7
, pp. 1287-1292
-
-
KURZROCK, R.1
ALBITAR, M.2
CORTES, J.E.3
-
80
-
-
16544382706
-
Dose-ranging pharmacodynamic study of tipifarnib (R115777) in patients with relapsed and refractory hematologic malignancies
-
ZIMMERMAN TM, HARLIN H, ODENIKE OM et al.: Dose-ranging pharmacodynamic study of tipifarnib (R115777) in patients with relapsed and refractory hematologic malignancies. J. Clin. Oncol. (2004) 22(23):4816-4822.
-
(2004)
J. Clin. Oncol
, vol.22
, Issue.23
, pp. 4816-4822
-
-
ZIMMERMAN, T.M.1
HARLIN, H.2
ODENIKE, O.M.3
-
81
-
-
34250703868
-
A Phase I study of the farnesyltransferase inhibitor tipifarnib in a week-on week-off dose schedule in acute myelogenous leukemia
-
KIRSCHBAUM M, SELWYN STEIN A, TUSCANO J et al.: A Phase I study of the farnesyltransferase inhibitor tipifarnib in a week-on week-off dose schedule in acute myelogenous leukemia. ASH Annual Meeting Abstracts (2006) 108(11):1948.
-
(1948)
ASH Annual Meeting Abstracts
, vol.108
, Issue.11
-
-
KIRSCHBAUM, M.1
SELWYN STEIN, A.2
TUSCANO, J.3
-
82
-
-
9444281436
-
The influence of farnesyl protein transferase inhibitor R115777 (Zarnestra) alone and in combination with purine nucleoside analogs on acute myeloid leukemia progenitors in vitro
-
KORYCKA A, SMOLEWSKI P, ROBAK T: The influence of farnesyl protein transferase inhibitor R115777 (Zarnestra) alone and in combination with purine nucleoside analogs on acute myeloid leukemia progenitors in vitro. Eur. J. Haematol. (2004) 73(6):418-426.
-
(2004)
Eur. J. Haematol
, vol.73
, Issue.6
, pp. 418-426
-
-
KORYCKA, A.1
SMOLEWSKI, P.2
ROBAK, T.3
-
83
-
-
33644921230
-
Tipifarnib: Farnesyl transferase inhibition at a crossroads
-
MESA RA: Tipifarnib: farnesyl transferase inhibition at a crossroads. Expert. Rev. Anticancer Ther. (2006) 6(3):313-319.
-
(2006)
Expert. Rev. Anticancer Ther
, vol.6
, Issue.3
, pp. 313-319
-
-
MESA, R.A.1
-
84
-
-
34250757247
-
Farnesyl transferase inhibitor (tipifarnib, zarnestra; Z) in combination with standard chemotherapy with idarubicin (Ida) and cytarabine (ara-C) for patients (pts) with newly diagnosed acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS)
-
ALVAREZ RH, KANTARJIAN H, GARCIA-MANERO G et al.: Farnesyl transferase inhibitor (tipifarnib, zarnestra; Z) in combination with standard chemotherapy with idarubicin (Ida) and cytarabine (ara-C) for patients (pts) with newly diagnosed acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS). ASH Annual Meeting Abstracts (2006) 108(11):1999.
-
(1999)
ASH Annual Meeting Abstracts
, vol.108
, Issue.11
-
-
ALVAREZ, R.H.1
KANTARJIAN, H.2
GARCIA-MANERO, G.3
-
85
-
-
34250735732
-
Active oral regimen for elderly adults with newly diagnosed acute myelogenous leukemia (AML): Phase I trial of oral tipifarnib (T) combined with oral etoposide (E) for adults ≥ age 70 who are not candidates for traditional cytotoxic chemotherapy (TCC)
-
KARP JE, FELDMAN EJ, MORRIS L et al.: Active oral regimen for elderly adults with newly diagnosed acute myelogenous leukemia (AML): Phase I trial of oral tipifarnib (T) combined with oral etoposide (E) for adults ≥ age 70 who are not candidates for traditional cytotoxic chemotherapy (TCC). ASH Annual Meeting Abstracts (2006) 108(11):426.
-
(2006)
ASH Annual Meeting Abstracts
, vol.108
, Issue.11
, pp. 426
-
-
KARP, J.E.1
FELDMAN, E.J.2
MORRIS, L.3
-
86
-
-
0035282735
-
Treatment of Bcr/Abl-positive acute lymphoblastic leukemia in P190 transgenic mice with the farnesyl transferase inhibitor SCH66336
-
REICHERT A, HEISTERKAMP N, DALEY GQ, GROFFEN J: Treatment of Bcr/Abl-positive acute lymphoblastic leukemia in P190 transgenic mice with the farnesyl transferase inhibitor SCH66336. Blood (2001) 97(5):1399-1403.
-
(2001)
Blood
, vol.97
, Issue.5
, pp. 1399-1403
-
-
REICHERT, A.1
HEISTERKAMP, N.2
DALEY, G.Q.3
GROFFEN, J.4
-
87
-
-
0035282901
-
Activity of the farnesyl protein transferase inhibitor SCH66336 against BCR/ABL-induced murine leukemia and primary cells from patients with chronic myeloid leukemia
-
PETERS DG, HOOVER RR, GERLACH MJ et al.: Activity of the farnesyl protein transferase inhibitor SCH66336 against BCR/ABL-induced murine leukemia and primary cells from patients with chronic myeloid leukemia. Blood (2001) 97(5):1404-1412.
-
(2001)
Blood
, vol.97
, Issue.5
, pp. 1404-1412
-
-
PETERS, D.G.1
HOOVER, R.R.2
GERLACH, M.J.3
-
88
-
-
0037945028
-
Sch-66336 (sarasar) and other benzocycloheptapyridyl farnesyl protein transferase inhibitors: Discovery, biology and clinical observations
-
TAVERAS AG, KIRSCHMEIER P, BAUM CM: Sch-66336 (sarasar) and other benzocycloheptapyridyl farnesyl protein transferase inhibitors: discovery, biology and clinical observations. Curr. Top. Med. Chem. (2003) 3(10):1103-1114.
-
(2003)
Curr. Top. Med. Chem
, vol.3
, Issue.10
, pp. 1103-1114
-
-
TAVERAS, A.G.1
KIRSCHMEIER, P.2
BAUM, C.M.3
-
89
-
-
0344611212
-
Efficacy of SCH66336, a farnesyl transferase inhibitor, in conjunction with imatinib against BCR-ABL-positive cells
-
NAKAJIMA A, TAUCHI T, SUMI M, BISHOP WR, OHYASHIKI K: Efficacy of SCH66336, a farnesyl transferase inhibitor, in conjunction with imatinib against BCR-ABL-positive cells. Mol. Cancer Ther. (2003) 2(3):219-224.
-
(2003)
Mol. Cancer Ther
, vol.2
, Issue.3
, pp. 219-224
-
-
NAKAJIMA, A.1
TAUCHI, T.2
SUMI, M.3
BISHOP, W.R.4
OHYASHIKI, K.5
-
90
-
-
0037369288
-
Apoptotic synergism between STI571 and the farnesyl transferase inhibitor SCH66336 on an imatinib-sensitive cell line
-
BRODSKY AL: Apoptotic synergism between STI571 and the farnesyl transferase inhibitor SCH66336 on an imatinib-sensitive cell line. Blood (2003) 101(5):2070.
-
(2003)
Blood
, vol.101
, Issue.5
, pp. 2070
-
-
BRODSKY, A.L.1
-
91
-
-
21744457612
-
Lonafarnib reduces the resistance of primitive quiescent CML cells to imatinib mesylate in vitro
-
JORGENSEN HG, ALLAN EK, GRAHAM SM et al.: Lonafarnib reduces the resistance of primitive quiescent CML cells to imatinib mesylate in vitro. Leukemia (2005) 19(7):1184-1191.
-
(2005)
Leukemia
, vol.19
, Issue.7
, pp. 1184-1191
-
-
JORGENSEN, H.G.1
ALLAN, E.K.2
GRAHAM, S.M.3
-
92
-
-
33744486584
-
Dasatinib (BMS-354825) targets an earlier progenitor population than imatinib in primary CML but does not eliminate the quiescent fraction
-
COPLAND M, HAMILTON A, ELRICK LJ et al.: Dasatinib (BMS-354825) targets an earlier progenitor population than imatinib in primary CML but does not eliminate the quiescent fraction. Blood (2006) 107(11):4532- 4539.
-
(2006)
Blood
, vol.107
, Issue.11
, pp. 4532-4539
-
-
COPLAND, M.1
HAMILTON, A.2
ELRICK, L.J.3
-
93
-
-
30744446226
-
Pilot study of lonafarnib, a farnesyl transferase inhibitor, in patients with chronic myeloid leukemia in the chronic or accelerated phase that is resistant or refractory to imatinib therapy
-
BORTHAKUR G, KANTARJIAN H, DALEY G et al.: Pilot study of lonafarnib, a farnesyl transferase inhibitor, in patients with chronic myeloid leukemia in the chronic or accelerated phase that is resistant or refractory to imatinib therapy. Cancer (2006) 106(2):346-352.
-
(2006)
Cancer
, vol.106
, Issue.2
, pp. 346-352
-
-
BORTHAKUR, G.1
KANTARJIAN, H.2
DALEY, G.3
-
94
-
-
0035886842
-
Preclinical antitumor activity of BMS-214662, a highly apoptotic and novel farnesyltransferase inhibitor
-
ROSE WC, LEE FY, FAIRCHILD CR et al.: Preclinical antitumor activity of BMS-214662, a highly apoptotic and novel farnesyltransferase inhibitor. Cancer Res. (2001) 61(20):7507-7517.
-
(2001)
Cancer Res
, vol.61
, Issue.20
, pp. 7507-7517
-
-
ROSE, W.C.1
LEE, F.Y.2
FAIRCHILD, C.R.3
-
95
-
-
21044459973
-
Phase I study of BMS-214662, a farnesyl transferase inhibitor in patients with acute leukemias and high-risk myelodysplastic syndromes
-
CORTES J, FADERL S, ESTEY E et al.: Phase I study of BMS-214662, a farnesyl transferase inhibitor in patients with acute leukemias and high-risk myelodysplastic syndromes. J. Clin. Oncol. (2005) 23(12):2805- 2812.
-
(2005)
J. Clin. Oncol
, vol.23
, Issue.12
, pp. 2805-2812
-
-
CORTES, J.1
FADERL, S.2
ESTEY, E.3
-
96
-
-
34548743285
-
BMS-214662 targets quiescent chronic myeloid leukaemia stem cells and enhances the activity of both imatinib and dasatinib (BMS-354825)
-
COPLAND M, HAMILTON A, ALLAN EK, BRUNTON V, HOLYOAKE TL: BMS-214662 targets quiescent chronic myeloid leukaemia stem cells and enhances the activity of both imatinib and dasatinib (BMS-354825). ASH Annual Meeting Abstracts (2005) 106(11):693.
-
(2005)
ASH Annual Meeting Abstracts
, vol.106
, Issue.11
, pp. 693
-
-
COPLAND, M.1
HAMILTON, A.2
ALLAN, E.K.3
BRUNTON, V.4
HOLYOAKE, T.L.5
-
97
-
-
0030923192
-
K- and N-Ras are geranylgeranylated in cells treated with farnesyl protein transferase inhibitors
-
WHYTE DB, KIRSCHMEIER P, HOCKENBERRY TN et al.: K- and N-Ras are geranylgeranylated in cells treated with farnesyl protein transferase inhibitors. J. Biol. Chem. (1997) 272(22):14459-14464.
-
(1997)
J. Biol. Chem
, vol.272
, Issue.22
, pp. 14459-14464
-
-
WHYTE, D.B.1
KIRSCHMEIER, P.2
HOCKENBERRY, T.N.3
-
98
-
-
0033231190
-
Geranylgeranylated RhoB mediates suppression of human tumor cell growth by farnesyltransferase inhibitors
-
DU W, PRENDERGAST GC: Geranylgeranylated RhoB mediates suppression of human tumor cell growth by farnesyltransferase inhibitors. Cancer Res. (1999) 59(21):5492-5496.
-
(1999)
Cancer Res
, vol.59
, Issue.21
, pp. 5492-5496
-
-
DU, W.1
PRENDERGAST, G.C.2
-
99
-
-
0034474092
-
Farnesyltransferase inhibitors: Antineoplastic properties, mechanisms of action, and clinical prospects
-
PRENDERGAST GC, OLIFF A: Farnesyltransferase inhibitors: antineoplastic properties, mechanisms of action, and clinical prospects. Semin. Cancer Biol. (2000) 10(6):443-452.
-
(2000)
Semin. Cancer Biol
, vol.10
, Issue.6
, pp. 443-452
-
-
PRENDERGAST, G.C.1
OLIFF, A.2
-
100
-
-
0034776102
-
The farnesyl transferase inhibitor SCH-66336 induces a G(2) → M or G(1) pause in sensitive human tumor cell lines
-
ASHAR HR, JAMES L, GRAY K et al.: The farnesyl transferase inhibitor SCH-66336 induces a G(2) → M or G(1) pause in sensitive human tumor cell lines. Exp. Cell Res. (2001) 262(1):17-27.
-
(2001)
Exp. Cell Res
, vol.262
, Issue.1
, pp. 17-27
-
-
ASHAR, H.R.1
JAMES, L.2
GRAY, K.3
-
101
-
-
0042978646
-
Centromere-associated protein-E is essential for the mammalian mitotic checkpoint to prevent aneuploidy due to single chromosome loss
-
WEAVER BA, BONDAY ZQ, PUTKEY FR, KOPS GJ, SILK AD, CLEVELAND DW: Centromere-associated protein-E is essential for the mammalian mitotic checkpoint to prevent aneuploidy due to single chromosome loss. J. Cell Biol. (2003) 162(4):551-563.
-
(2003)
J. Cell Biol
, vol.162
, Issue.4
, pp. 551-563
-
-
WEAVER, B.A.1
BONDAY, Z.Q.2
PUTKEY, F.R.3
KOPS, G.J.4
SILK, A.D.5
CLEVELAND, D.W.6
-
102
-
-
0345689346
-
Farnesyltransferase inhibitors in hematologic malignancies: New horizons in therapy
-
LANCET JE, KARP JE: Farnesyltransferase inhibitors in hematologic malignancies: new horizons in therapy. Blood (2003) 102(12):3880- 3889.
-
(2003)
Blood
, vol.102
, Issue.12
, pp. 3880-3889
-
-
LANCET, J.E.1
KARP, J.E.2
-
103
-
-
0033986790
-
The phosphoinositide 3-OH kinase/AKT2 pathway as a critical target for farnesyltransferase inhibitor-induced apoptosis
-
JIANG K, COPPOLA D, CRESPO NC et al.: The phosphoinositide 3-OH kinase/AKT2 pathway as a critical target for farnesyltransferase inhibitor-induced apoptosis. Mol. and Biol. (2000) 20(1):139-148.
-
(2000)
Mol. and Biol
, vol.20
, Issue.1
, pp. 139-148
-
-
JIANG, K.1
COPPOLA, D.2
CRESPO, N.C.3
-
104
-
-
0035887454
-
The farnesyl protein transferase inhibitor SCH-66336 is a potent inhibitor of MDR1 product P-glycoprotein
-
WANG E, CASCIANO CN, CLEMENT RP, JOHNSON WW: The farnesyl protein transferase inhibitor SCH-66336 is a potent inhibitor of MDR1 product P-glycoprotein. Cancer Res. (2001) 61(20):7525-7529.
-
(2001)
Cancer Res
, vol.61
, Issue.20
, pp. 7525-7529
-
-
WANG, E.1
CASCIANO, C.N.2
CLEMENT, R.P.3
JOHNSON, W.W.4
-
105
-
-
0035216833
-
Farnesyltransferase inhibitors: Mechanism and applications
-
PRENDERGAST GC, RANE N: Farnesyltransferase inhibitors: mechanism and applications. Expert. Opin. Investig. Drugs (2001) 10(12):2105- 2116.
-
(2001)
Expert. Opin. Investig. Drugs
, vol.10
, Issue.12
, pp. 2105-2116
-
-
PRENDERGAST, G.C.1
RANE, N.2
-
106
-
-
26444574802
-
Development of farnesyl transferase inhibitors: A review
-
APPELS NM, BEIJNEN JH, SCHELLENS JH: Development of farnesyl transferase inhibitors: a review. Oncologist (2005) 10(8):565-578.
-
(2005)
Oncologist
, vol.10
, Issue.8
, pp. 565-578
-
-
APPELS, N.M.1
BEIJNEN, J.H.2
SCHELLENS, J.H.3
-
107
-
-
0028959539
-
Farnesyl derivatives of rigid carboxylic acids-inhibitors of ras-dependent cell growth
-
MARCIANO D, BEN-BARUCH G, MAROM M, EGOZI Y, HAKLAI R, KLOOG Y: Farnesyl derivatives of rigid carboxylic acids-inhibitors of ras-dependent cell growth. J. Med. Chem. (1995) 38(8):1267-1272.
-
(1995)
J. Med. Chem
, vol.38
, Issue.8
, pp. 1267-1272
-
-
MARCIANO, D.1
BEN-BARUCH, G.2
MAROM, M.3
EGOZI, Y.4
HAKLAI, R.5
KLOOG, Y.6
-
108
-
-
0033803477
-
RAS inhibitors: Potential for cancer rherapeutics
-
KLOOG Y, COX AD: RAS inhibitors: potential for cancer rherapeutics. Mol. Med. Today (2000) 6(10):398-402.
-
(2000)
Mol. Med. Today
, vol.6
, Issue.10
, pp. 398-402
-
-
KLOOG, Y.1
COX, A.D.2
-
109
-
-
0028981375
-
Selective inhibition of Ras-dependent cell growth by farnesylthiosalisylic acid
-
MAROM M, HAKLAI R, BEN-BARUCH G, MARCIANO D, EGOZI Y, KLOOG Y: Selective inhibition of Ras-dependent cell growth by farnesylthiosalisylic acid. J. Biol. Chem. (1995) 270(38):22263-22270.
-
(1995)
J. Biol. Chem
, vol.270
, Issue.38
, pp. 22263-22270
-
-
MAROM, M.1
HAKLAI, R.2
BEN-BARUCH, G.3
MARCIANO, D.4
EGOZI, Y.5
KLOOG, Y.6
-
110
-
-
0032477606
-
Dislodgment and accelerated degradation of Ras
-
HAKLAI R, WEISZ MG, ELAD G et al.: Dislodgment and accelerated degradation of Ras. Biochemistry (1998) 37(5):1306-1314.
-
(1998)
Biochemistry
, vol.37
, Issue.5
, pp. 1306-1314
-
-
HAKLAI, R.1
WEISZ, M.G.2
ELAD, G.3
-
111
-
-
0032717429
-
Targeting of K-Ras 4B by S-trans, trans-farnesyl thiosalicylic acid
-
ELAD G, PAZ A, HAKLAI R, MARCIANO D, COX A, KLOOG Y: Targeting of K-Ras 4B by S-trans, trans-farnesyl thiosalicylic acid. Biochim. Biophys. Acta. (1999) 1452(3):228-242.
-
(1999)
Biochim. Biophys. Acta
, vol.1452
, Issue.3
, pp. 228-242
-
-
ELAD, G.1
PAZ, A.2
HAKLAI, R.3
MARCIANO, D.4
COX, A.5
KLOOG, Y.6
-
112
-
-
0037150157
-
Functional inhibition of Ras by S-trans, trans-farnesyl thiosalicylic acid attenuates atherosclerosis in apolipoprotein E knockout mice
-
GEORGE J, AFEK A, KEREN P et al.: Functional inhibition of Ras by S-trans, trans-farnesyl thiosalicylic acid attenuates atherosclerosis in apolipoprotein E knockout mice. Circulation (2002) 105(20):2416- 2422.
-
(2002)
Circulation
, vol.105
, Issue.20
, pp. 2416-2422
-
-
GEORGE, J.1
AFEK, A.2
KEREN, P.3
-
113
-
-
0033555935
-
Membrane interactions of a constitutively active GFP-Ki-Ras 4B and their role in signaling. Evidence from lateral mobility studies
-
NIV H, GUTMAN O, HENIS YI, KLOOG Y: Membrane interactions of a constitutively active GFP-Ki-Ras 4B and their role in signaling. Evidence from lateral mobility studies. J. Biol. Chem. (1999) 274(3):1606-1613.
-
(1999)
J. Biol. Chem
, vol.274
, Issue.3
, pp. 1606-1613
-
-
NIV, H.1
GUTMAN, O.2
HENIS, Y.I.3
KLOOG, Y.4
-
114
-
-
2342508517
-
Galectin-1(L11A) predicted from a computed galectin-1 farnesyl-binding pocket selectively inhibits Ras-GTP
-
ROTBLAT B, NIV H, ANDRE S, KALTNER H, GABIUS HJ, KLOOG Y: Galectin-1(L11A) predicted from a computed galectin-1 farnesyl-binding pocket selectively inhibits Ras-GTP. Cancer Res. (2004) 64(9):3112-3118.
-
(2004)
Cancer Res
, vol.64
, Issue.9
, pp. 3112-3118
-
-
ROTBLAT, B.1
NIV, H.2
ANDRE, S.3
KALTNER, H.4
GABIUS, H.J.5
KLOOG, Y.6
-
115
-
-
0031590420
-
The Ras antagonist 5-farnesylthiosalicylic acid induces inhibition of MAPK activation
-
GANA-WEISZ M, HAKLAI R, MARCIANO D, EGOZI Y, BEN-BARUCH G, KLOOG Y: The Ras antagonist 5-farnesylthiosalicylic acid induces inhibition of MAPK activation. Biochem. Biophys. Res. Commun. (1997) 239(3):900-904.
-
(1997)
Biochem. Biophys. Res. Commun
, vol.239
, Issue.3
, pp. 900-904
-
-
GANA-WEISZ, M.1
HAKLAI, R.2
MARCIANO, D.3
EGOZI, Y.4
BEN-BARUCH, G.5
KLOOG, Y.6
-
116
-
-
20444438759
-
Disruption of cooperation between Ras and MycN in human neuroblastoma cells promotes growrh arrest
-
YAARI S, JACOB-HIRSCH J, AMARIGLIO N, HAKLAI R, RECHAVI G, KLOOG Y: Disruption of cooperation between Ras and MycN in human neuroblastoma cells promotes growrh arrest. Clin. Cancer Res. (2005) 11(12):4321-4330.
-
(2005)
Clin. Cancer Res
, vol.11
, Issue.12
, pp. 4321-4330
-
-
YAARI, S.1
JACOB-HIRSCH, J.2
AMARIGLIO, N.3
HAKLAI, R.4
RECHAVI, G.5
KLOOG, Y.6
-
117
-
-
13444283313
-
Ras inhibition in glioblastoma down-regulates hypoxia-inducible factor-1alpha, causing glycolysis shutdown and cell death
-
BLUM R, JACOB-HIRSCH J, AMARIGLIO N, RECHAVI G, KLOOG Y: Ras inhibition in glioblastoma down-regulates hypoxia-inducible factor-1alpha, causing glycolysis shutdown and cell death. Cancer Res. (2005) 65(3):999-1006.
-
(2005)
Cancer Res
, vol.65
, Issue.3
, pp. 999-1006
-
-
BLUM, R.1
JACOB-HIRSCH, J.2
AMARIGLIO, N.3
RECHAVI, G.4
KLOOG, Y.5
-
118
-
-
0033559885
-
Growth inhibition of ras-dependent tumors in nude mice by a potent ras-disiodging antagonist
-
EGOZI Y, WEISZ B, GANA-WEISZ M, BEN-BARUCH G, KLOOG Y: Growth inhibition of ras-dependent tumors in nude mice by a potent ras-disiodging antagonist. Int. J. Cancer (1999) 80(6):911-918.
-
(1999)
Int. J. Cancer
, vol.80
, Issue.6
, pp. 911-918
-
-
EGOZI, Y.1
WEISZ, B.2
GANA-WEISZ, M.3
BEN-BARUCH, G.4
KLOOG, Y.5
-
120
-
-
0013227128
-
A new functional Ras antagonist inhibits human pancreatic tumor growth in nude mice
-
WEISZ B, GIEHL K, GANA-WEISZ M et al.: A new functional Ras antagonist inhibits human pancreatic tumor growth in nude mice. Oncogene (1999) 18(16):2579-2588.
-
(1999)
Oncogene
, vol.18
, Issue.16
, pp. 2579-2588
-
-
WEISZ, B.1
GIEHL, K.2
GANA-WEISZ, M.3
-
121
-
-
0033400494
-
Farnesylthiosalicyclic acid inhibits the growth of human Merkel cell carcinoma in SCID mice
-
JANSEN B, HEERE-RESS E, SCHLAGBAUER-WADL H et al.: Farnesylthiosalicyclic acid inhibits the growth of human Merkel cell carcinoma in SCID mice. J. Mol. Med. (1999) 77(11):792-797.
-
(1999)
J. Mol. Med
, vol.77
, Issue.11
, pp. 792-797
-
-
JANSEN, B.1
HEERE-RESS, E.2
SCHLAGBAUER-WADL, H.3
-
122
-
-
0034252166
-
A novel Ras antagonist regulates both oncogenic Ras and the tumor suppressor p53 in colon cancer cells
-
HALASCHEK-WIENER J, WACHECK V, SCHLAGBAUER-WADL H, WOLFF K, KLOOG Y, JANSEN B: A novel Ras antagonist regulates both oncogenic Ras and the tumor suppressor p53 in colon cancer cells. Mol. Med. (2000) 6(8):693-704.
-
(2000)
Mol. Med
, vol.6
, Issue.8
, pp. 693-704
-
-
HALASCHEK-WIENER, J.1
WACHECK, V.2
SCHLAGBAUER-WADL, H.3
WOLFF, K.4
KLOOG, Y.5
JANSEN, B.6
-
123
-
-
0034735895
-
Disruption of TGF-beta growth inhibition by oncogenic ras is linked to p27Kip1 mislocalization
-
LIU X, SUN Y, EHRLICH M et al.: Disruption of TGF-beta growth inhibition by oncogenic ras is linked to p27Kip1 mislocalization. Oncogene (2000) 19(51):5926-5935.
-
(2000)
Oncogene
, vol.19
, Issue.51
, pp. 5926-5935
-
-
LIU, X.1
SUN, Y.2
EHRLICH, M.3
|