-
1
-
-
0034615568
-
Structure and function of the methionine aminopeptidases
-
Lowther WT, Matthews BW. Structure and function of the methionine aminopeptidases. Biochim Biophys Acta 2000;1477:157-67.
-
(2000)
Biochim Biophys Acta
, vol.1477
, pp. 157-167
-
-
Lowther, W.T.1
Matthews, B.W.2
-
4
-
-
0029186022
-
Prediction of the coding sequences of unidentified human genes. III. The coding sequences of 40 new genes (KIAA0081-KIAA0120) deduced by analysis of cDNA clones from human cell line KG-1
-
Nagase T, Miyajima N, Tanaka A, et al. Prediction of the coding sequences of unidentified human genes. III. The coding sequences of 40 new genes (KIAA0081-KIAA0120) deduced by analysis of cDNA clones from human cell line KG-1. DNA Res 1995;2:37-43.
-
(1995)
DNA Res
, vol.2
, pp. 37-43
-
-
Nagase, T.1
Miyajima, N.2
Tanaka, A.3
-
5
-
-
0025204095
-
Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth
-
Ingber D, Fujita T, Kishimoto S, et al. Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth. Nature (Lond.) 1990;348:555-7.
-
(1990)
Nature (Lond)
, vol.348
, pp. 555-557
-
-
Ingber, D.1
Fujita, T.2
Kishimoto, S.3
-
6
-
-
0030924753
-
The anti-angiogenic agent fumagillin covalently binds and inhibits the methionine aminopeptidase, MetAP-2
-
Sin N, Meng L, Wang MQW, Wen JJ, Bornmann WG, Crews CM. The anti-angiogenic agent fumagillin covalently binds and inhibits the methionine aminopeptidase, MetAP-2. Proc Natl Acad Sci USA 1997;94:6099-103.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 6099-6103
-
-
Sin, N.1
Meng, L.2
Wang, M.Q.W.3
Wen, J.J.4
Bornmann, W.G.5
Crews, C.M.6
-
7
-
-
0031171961
-
Methionine aminopeptidase (type 2) is the common target for angiogenesis inhibitors AGM-1470 and ovalicin
-
Griffith EC, Su Z, Turk BE, et al. Methionine aminopeptidase (type 2) is the common target for angiogenesis inhibitors AGM-1470 and ovalicin. Chem Biol 1997;4:461-71.
-
(1997)
Chem Biol
, vol.4
, pp. 461-471
-
-
Griffith, E.C.1
Su, Z.2
Turk, B.E.3
-
8
-
-
0034120430
-
TNP-470: An angiogenesis inhibitor in clinical development for cancer
-
Kruger EA, Figg WD. TNP-470: an angiogenesis inhibitor in clinical development for cancer. Exp Opin Investig Drugs 2000;9:1383-96.
-
(2000)
Exp Opin Investig Drugs
, vol.9
, pp. 1383-1396
-
-
Kruger, E.A.1
Figg, W.D.2
-
9
-
-
0034901968
-
Phase I trial of the angiogenesis inhibitor TNP-470 for progressive androgen-independent prostate cancer
-
Logothetis CJ, Wu KK, Finn LD, et al. Phase I trial of the angiogenesis inhibitor TNP-470 for progressive androgen-independent prostate cancer. Clin Cancer Res 2001;7:1198-203.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 1198-1203
-
-
Logothetis, C.J.1
Wu, K.K.2
Finn, L.D.3
-
10
-
-
9144222006
-
Proteomics based target identification: Bengamides as a new class of methionine aminopeptidase inhibitors
-
Towbin H, Bair KW, DeCaprio JA, et al. Proteomics based target identification: Bengamides as a new class of methionine aminopeptidase inhibitors. J Biol Chem 2003;278:52964-71.
-
(2003)
J Biol Chem
, vol.278
, pp. 52964-52971
-
-
Towbin, H.1
Bair, K.W.2
DeCaprio, J.A.3
-
12
-
-
0035950061
-
Synthesis and antitumor activity of ester-modified analogues of bengamide B
-
Kinder FR, Versace RW, Bair KB, et al. Synthesis and antitumor activity of ester-modified analogues of bengamide B. J Med Chem 2001;44:3692-9.
-
(2001)
J Med Chem
, vol.44
, pp. 3692-3699
-
-
Kinder, F.R.1
Versace, R.W.2
Bair, K.B.3
-
13
-
-
0035942736
-
Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells
-
Elbashir SM, Harborth J, Lendeckel W, Yalcin A, Weber K, Tuschl T. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature (Lond.) 2001;411:494-8.
-
(2001)
Nature (Lond)
, vol.411
, pp. 494-498
-
-
Elbashir, S.M.1
Harborth, J.2
Lendeckel, W.3
Yalcin, A.4
Weber, K.5
Tuschl, T.6
-
14
-
-
13044300888
-
Molecular recognition of angiogenesis inhibitors fumagillin and ovalicin by methionine aminopeptidase 2
-
Griffith EC, Su Z, Niwayama S, Ramsay CA, Chang Y-H, Liu JO. Molecular recognition of angiogenesis inhibitors fumagillin and ovalicin by methionine aminopeptidase 2. Proc Natl Acad Sci USA 1998;95:15183-8.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 15183-15188
-
-
Griffith, E.C.1
Su, Z.2
Niwayama, S.3
Ramsay, C.A.4
Chang, Y.-H.5
Liu, J.O.6
-
15
-
-
0032515029
-
Structure of human methionine aminopeptidase-2 complexed with fumagillin
-
Liu S, Widom J, Kemp CW, Crews CM, Clardy J. Structure of human methionine aminopeptidase-2 complexed with fumagillin. Science (Wash. DC) 1998;282;1324-7.
-
(1998)
Science (Wash DC)
, vol.282
, pp. 1324-1327
-
-
Liu, S.1
Widom, J.2
Kemp, C.W.3
Crews, C.M.4
Clardy, J.5
-
16
-
-
0347993051
-
An unusual peptide deformylase features in the human mitochondrial N-terminal methionine excision pathway
-
Serero A, Giglione C, Sardini A, Martinez-Sanz J, Meinnel T. An unusual peptide deformylase features in the human mitochondrial N-terminal methionine excision pathway. J Biol Chem 2003;278:52953-63.
-
(2003)
J Biol Chem
, vol.278
, pp. 52953-52963
-
-
Serero, A.1
Giglione, C.2
Sardini, A.3
Martinez-Sanz, J.4
Meinnel, T.5
-
17
-
-
85081427472
-
Inhibition of primary tumor growth by PPI-2458, a methionine aminopeptidase-2 inhibitor: Dose and schedule responses
-
abstract no. A174
-
Lazarus DD, Bernier SG, Labenski MT, et al. Inhibition of primary tumor growth by PPI-2458, a methionine aminopeptidase-2 inhibitor: dose and schedule responses. AACR-EORTC International Conference, abstract no. A174 2003.
-
(2003)
AACR-EORTC International Conference
-
-
Lazarus, D.D.1
Bernier, S.G.2
Labenski, M.T.3
|