-
1
-
-
52949127312
-
An integrated genomic analysis of human glioblastoma multiforme
-
Parsons DW, Jones S, Zhang X, Lin JC-H, Leary RJ, Angenendt P, et al. An integrated genomic analysis of human glioblastoma multiforme. Science 2008;321:1807-12.
-
(2008)
Science
, vol.321
, pp. 1807-1812
-
-
Parsons, D.W.1
Jones, S.2
Zhang, X.3
Lin, J.-H.4
Leary, R.J.5
Angenendt, P.6
-
2
-
-
67649321430
-
Proteasomal and genetic inactivation of the NF1 tumor suppressor in gliomagenesis
-
McGillicuddy LT, Fromm JA, Hollstein PE, Kubek S, Beroukhim R, De Raedt T, et al. Proteasomal and genetic inactivation of the NF1 tumor suppressor in gliomagenesis. Cancer Cell 2009;16:44-54.
-
(2009)
Cancer Cell
, vol.16
, pp. 44-54
-
-
McGillicuddy, L.T.1
Fromm, J.A.2
Hollstein, P.E.3
Kubek, S.4
Beroukhim, R.5
de Raedt, T.6
-
3
-
-
0027439597
-
Neurofibromatosis type 1 gene mutations in neuroblastoma
-
The I, Murthy AE, Hannigan GE, Jacoby LB, Menon AG, Gusella JF, et al. Neurofibromatosis type 1 gene mutations in neuroblastoma. Nat Genet 1993;3:62-6.
-
(1993)
Nat Genet
, vol.3
, pp. 62-66
-
-
The, I.1
Murthy, A.E.2
Hannigan, G.E.3
Jacoby, L.B.4
Menon, A.G.5
Gusella, J.F.6
-
4
-
-
84876037369
-
Elucidating distinct roles for NF1 in melanomagenesis
-
Maertens O, Johnson B, Hollstein P, Frederick DT, Cooper ZA, Messiaen L, et al. Elucidating distinct roles for NF1 in melanomagenesis. Cancer Discov 2013;3:338-49.
-
(2013)
Cancer Discov
, vol.3
, pp. 338-349
-
-
Maertens, O.1
Johnson, B.2
Hollstein, P.3
Frederick, D.T.4
Cooper, Z.A.5
Messiaen, L.6
-
5
-
-
54549094903
-
Somatic mutations affect key pathways in lung adenocarcinoma
-
Ding L, Getz G, Wheeler DA, Mardis ER, McLellan MD, Cibulskis K, et al. Somatic mutations affect key pathways in lung adenocarcinoma. Nature 2008;455:1069-75.
-
(2008)
Nature
, vol.455
, pp. 1069-1075
-
-
Ding, L.1
Getz, G.2
Wheeler, D.A.3
Mardis, E.R.4
McLellan, M.D.5
Cibulskis, K.6
-
6
-
-
0025251137
-
The GAP-related domain of the neurofibromatosis type 1 gene product interacts with ras p21
-
Martin GA, Viskochil D, Bollag G, McCabe PC, Crosier WJ, Haubruck H, et al. The GAP-related domain of the neurofibromatosis type 1 gene product interacts with ras p21. Cell 1990;63:843-9.
-
(1990)
Cell
, vol.63
, pp. 843-849
-
-
Martin, G.A.1
Viskochil, D.2
Bollag, G.3
McCabe, P.C.4
Crosier, W.J.5
Haubruck, H.6
-
7
-
-
0025326726
-
A major segment of the neurofibromatosis type 1 gene: CDNA sequence, genomic structure, and point mutations
-
Cawthon RM, Weiss R, Xu GF, Viskochil D, Culver M, Stevens J, et al. A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. Cell 1990;62: 193-201.
-
(1990)
Cell
, vol.62
, pp. 193-201
-
-
Cawthon, R.M.1
Weiss, R.2
Xu, G.F.3
Viskochil, D.4
Culver, M.5
Stevens, J.6
-
8
-
-
84882475880
-
Chemotherapy for the treatment of malignant peripheral nerve sheath tumors in neurofibromatosis 1: A 10-year institutional review
-
Zehou O, Fabre E, Zelek L, Sbidian E, Ortonne N, Banu E, et al. Chemotherapy for the treatment of malignant peripheral nerve sheath tumors in neurofibromatosis 1: a 10-year institutional review. Orphanet J Rare Dis 2013;8:127.
-
(2013)
Orphanet J Rare Dis
, vol.8
, pp. 127
-
-
Zehou, O.1
Fabre, E.2
Zelek, L.3
Sbidian, E.4
Ortonne, N.5
Banu, E.6
-
9
-
-
0036096489
-
Malignant peripheral nerve sheath tumours in neurofibromatosis 1
-
Evans DGR, Baser ME, McGaughran J, Sharif S, Howard E, Moran A. Malignant peripheral nerve sheath tumours in neurofibromatosis 1. J Med Genet 2002;39:311-4.
-
(2002)
J Med Genet
, vol.39
, pp. 311-314
-
-
Evans, D.G.R.1
Baser, M.E.2
McGaughran, J.3
Sharif, S.4
Howard, E.5
Moran, A.6
-
10
-
-
65349183575
-
Survival in malignant peripheral nerve sheath tumours: A comparison between sporadic and neurofibromatosis type 1-associated tumours
-
Porter DE, Prasad V, Foster L, Dall GF, Birch R, Grimer R.J. Survival in malignant peripheral nerve sheath tumours: a comparison between sporadic and neurofibromatosis type 1-associated tumours. Sarcoma 2009;2009:756395.
-
(2009)
Sarcoma
, vol.2009
, pp. 756395
-
-
Porter, D.E.1
Prasad, V.2
Foster, L.3
Dall, G.F.4
Birch, R.5
Grimer, R.J.6
-
11
-
-
0026528368
-
Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis
-
DeClue JE, Papageorge AG, Fletcher JA, Diehl SR, Ratner N, Vass WC, et al. Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis. Cell 1992;69:265-73.
-
(1992)
Cell
, vol.69
, pp. 265-273
-
-
Declue, J.E.1
Papageorge, A.G.2
Fletcher, J.A.3
Diehl, S.R.4
Ratner, N.5
Vass, W.C.6
-
12
-
-
84863594749
-
Sensitivity of glioblastomas to clinically available MEK inhibitors is defined by neurofibromin 1 deficiency
-
See WL, Tan I-L, Mukherjee J, Nicolaides T, Pieper R.O. Sensitivity of glioblastomas to clinically available MEK inhibitors is defined by neurofibromin 1 deficiency. Cancer Res 2012;72:3350-9.
-
(2012)
Cancer Res
, vol.72
, pp. 3350-3359
-
-
See, W.L.1
Tan, I.-L.2
Mukherjee, J.3
Nicolaides, T.4
Pieper, R.O.5
-
13
-
-
44449093081
-
TORC1 is essential for NF1-associated malignancies
-
Johannessen CM, Johnson BW, Williams SMG, Chan AW, Reczek EE, Lynch RC, et al. TORC1 is essential for NF1-associated malignancies. Curr Biol 2008;18:56-62.
-
(2008)
Curr Biol
, vol.18
, pp. 56-62
-
-
Johannessen, C.M.1
Johnson, B.W.2
Williams, S.M.G.3
Chan, A.W.4
Reczek, E.E.5
Lynch, R.C.6
-
14
-
-
84872546604
-
Prognostic significance of AKT/mTOR and MAPK pathways and antitumor effect of mTOR inhibitor in NF1-related and sporadic malignant peripheral nerve sheath tumors
-
Endo M, Yamamoto H, Setsu N, Kohashi K, Takahashi Y, Ishii T, et al. Prognostic significance of AKT/mTOR and MAPK pathways and antitumor effect of mTOR inhibitor in NF1-related and sporadic malignant peripheral nerve sheath tumors. Clin Cancer Res 2013;19:450-61.
-
(2013)
Clin Cancer Res
, vol.19
, pp. 450-461
-
-
Endo, M.1
Yamamoto, H.2
Setsu, N.3
Kohashi, K.4
Takahashi, Y.5
Ishii, T.6
-
15
-
-
77955737728
-
NF1 inactivation in adult acute myelogenous leukemia
-
Parkin B, Ouillette P, Wang Y, Liu Y, Wright W, Roulston D, et al. NF1 inactivation in adult acute myelogenous leukemia. Clin Cancer Res 2010;16:4135-47.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 4135-4147
-
-
Parkin, B.1
Ouillette, P.2
Wang, Y.3
Liu, Y.4
Wright, W.5
Roulston, D.6
-
16
-
-
84878652051
-
PI3K and MEK inhibitor combinations: Examining the evidence in selected tumor types
-
Britten C.D. PI3K and MEK inhibitor combinations: examining the evidence in selected tumor types. Cancer Chemother Pharmacol 2013;71:1395-409.
-
(2013)
Cancer Chemother Pharmacol
, vol.71
, pp. 1395-1409
-
-
Britten, C.D.1
-
17
-
-
20844435467
-
The NF1 tumor suppressor critically regulates TSC2 and mTOR
-
Johannessen CM, Reczek EE, James MF, Brems H, Legius E, Cichowski K. The NF1 tumor suppressor critically regulates TSC2 and mTOR. Proc Natl Acad Sci U S A 2005;102:8573-8.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 8573-8578
-
-
Johannessen, C.M.1
Reczek, E.E.2
James, M.F.3
Brems, H.4
Legius, E.5
Cichowski, K.6
-
18
-
-
11144358645
-
High frequency of mutations of the PIK3CA gene in human cancers
-
Samuels Y, Wang Z, Bardelli A, Silliman N, Ptak J, Szabo S, et al. High frequency of mutations of the PIK3CA gene in human cancers. Science 2004;304:554.
-
(2004)
Science
, vol.304
, pp. 554
-
-
Samuels, Y.1
Wang, Z.2
Bardelli, A.3
Silliman, N.4
Ptak, J.5
Szabo, S.6
-
19
-
-
49649087385
-
Essential roles of PI(3)K-p110beta in cell growth, metabolism and tumorigenesis
-
Jia S, Liu Z, Zhang S, Liu P, Zhang L, Lee SH, et al. Essential roles of PI(3)K-p110beta in cell growth, metabolism and tumorigenesis. Nature 2008;454:776-9.
-
(2008)
Nature
, vol.454
, pp. 776-779
-
-
Jia, S.1
Liu, Z.2
Zhang, S.3
Liu, P.4
Zhang, L.5
Lee, S.H.6
-
20
-
-
77957201023
-
Phosphatidylinositol 3-kinase-δinhibitor CAL-101 shows promising preclinical activity in chronic lymphocytic leukemia by antagonizing intrinsic and extrinsic cellular survival signals
-
Herman SEM, Gordon AL, Wagner AJ, Heerema NA, Zhao W, Flynn JM, et al. Phosphatidylinositol 3-kinase-δinhibitor CAL-101 shows promising preclinical activity in chronic lymphocytic leukemia by antagonizing intrinsic and extrinsic cellular survival signals. Blood 2010;116:2078-88.
-
(2010)
Blood
, vol.116
, pp. 2078-2088
-
-
Herman, S.E.M.1
Gordon, A.L.2
Wagner, A.J.3
Heerema, N.A.4
Zhao, W.5
Flynn, J.M.6
-
21
-
-
79960794613
-
A drug targeting only p110αcan block phosphoinositide 3-kinase signalling and tumour growth in certain cell types
-
Jamieson S, Flanagan JU, Kolekar S, Buchanan C, Kendall JD, Lee W-J, et al. A drug targeting only p110αcan block phosphoinositide 3-kinase signalling and tumour growth in certain cell types. Biochem J 2011;438:53-62.
-
(2011)
Biochem J
, vol.438
, pp. 53-62
-
-
Jamieson, S.1
Flanagan, J.U.2
Kolekar, S.3
Buchanan, C.4
Kendall, J.D.5
Lee, W.-J.6
-
22
-
-
78751553221
-
CAL-101, a p110delta selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability
-
Lannutti BJ, Meadows SA, Herman SEM, Kashishian A, Steiner B, Johnson AJ, et al. CAL-101, a p110delta selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability. Blood 2011;117:591-4.
-
(2011)
Blood
, vol.117
, pp. 591-594
-
-
Lannutti, B.J.1
Meadows, S.A.2
Herman, S.E.M.3
Kashishian, A.4
Steiner, B.5
Johnson, A.J.6
-
23
-
-
84866876711
-
Human target validation of phosphoinositide 3-kinase (PI3K)β: Effects on platelets and insulin sensitivity, using AZD6482 a novel PI3Kβinhibitor
-
Nylander S, Kull B, Björkman JA, Ulvinge JC, Oakes N, Emanuelsson BM, et al. Human target validation of phosphoinositide 3-kinase (PI3K)β: effects on platelets and insulin sensitivity, using AZD6482 a novel PI3Kβinhibitor. J Thromb Haemost 2012;10:2127-36.
-
(2012)
J Thromb Haemost
, vol.10
, pp. 2127-2136
-
-
Nylander, S.1
Kull, B.2
Björkman, J.A.3
Ulvinge, J.C.4
Oakes, N.5
Emanuelsson, B.M.6
-
24
-
-
52449106253
-
The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer
-
Folkes AJ, Ahmadi K, Alderton WK, Alix S, Baker SJ, Box G, et al. The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer. J Med Chem 2008;51:5522-32.
-
(2008)
J Med Chem
, vol.51
, pp. 5522-5532
-
-
Folkes, A.J.1
Ahmadi, K.2
Alderton, W.K.3
Alix, S.4
Baker, S.J.5
Box, G.6
-
25
-
-
0036753494
-
Two TOR complexes, only one of which is rapamycin sensitive, have distinct roles in cell growth control
-
Loewith R, Jacinto E, Wullschleger S, Lorberg A, Crespo JL, Bonenfant D, et al. Two TOR complexes, only one of which is rapamycin sensitive, have distinct roles in cell growth control. Mol Cell 2002;10:457-68.
-
(2002)
Mol Cell
, vol.10
, pp. 457-468
-
-
Loewith, R.1
Jacinto, E.2
Wullschleger, S.3
Lorberg, A.4
Crespo, J.L.5
Bonenfant, D.6
-
26
-
-
13844312400
-
Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex
-
Sarbassov DD, Guertin DA, Ali SM, Sabatini D.M. Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex. Science 2005;307:1098-101.
-
(2005)
Science
, vol.307
, pp. 1098-1101
-
-
Sarbassov, D.D.1
Guertin, D.A.2
Ali, S.M.3
Sabatini, D.M.4
-
27
-
-
59749091850
-
A complex interplay between Akt, TSC2 and the two mTOR complexes
-
Huang J, Manning B.D. A complex interplay between Akt, TSC2 and the two mTOR complexes. Biochem Soc Trans 2009;37:217-22.
-
(2009)
Biochem Soc Trans
, vol.37
, pp. 217-222
-
-
Huang, J.1
Manning, B.D.2
-
28
-
-
3342895823
-
Rictor, a novel binding partner of mTOR, defines a rapamycin-insensitive and raptor-independent pathway that regulates the cytoskeleton
-
Sarbassov DD, Ali SM, Kim D-H, Guertin DA, Latek RR, Erdjument-Bromage H, et al. Rictor, a novel binding partner of mTOR, defines a rapamycin-insensitive and raptor-independent pathway that regulates the cytoskeleton. Curr Biol 2004;14:1296-302.
-
(2004)
Curr Biol
, vol.14
, pp. 1296-1302
-
-
Sarbassov, D.D.1
Ali, S.M.2
Kim, D.-H.3
Guertin, D.A.4
Latek, R.R.5
Erdjument-Bromage, H.6
-
29
-
-
77954615408
-
MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo
-
Hirai H, Sootome H, Nakatsuru Y, Miyama K, Taguchi S, Tsujioka K, et al. MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo. Mol Cancer Ther 2010;9:1956-67.
-
(2010)
Mol Cancer Ther
, vol.9
, pp. 1956-1967
-
-
Hirai, H.1
Sootome, H.2
Nakatsuru, Y.3
Miyama, K.4
Taguchi, S.5
Tsujioka, K.6
-
30
-
-
0032763861
-
Mouse models of tumor development in neurofibromatosis type 1
-
Cichowski K, Shih TS, Schmitt E, Santiago S, Reilly K, McLaughlin ME, et al. Mouse models of tumor development in neurofibromatosis type 1. Science 1999;286:2172-6.
-
(1999)
Science
, vol.286
, pp. 2172-2176
-
-
Cichowski, K.1
Shih, T.S.2
Schmitt, E.3
Santiago, S.4
Reilly, K.5
McLaughlin, M.E.6
-
31
-
-
80052557069
-
Exploiting cancer cell vulnerabilities to develop a combination therapy for ras-driven tumors
-
De Raedt T, Walton Z, Yecies JL, Li D, Chen Y, Malone CF, et al. Exploiting cancer cell vulnerabilities to develop a combination therapy for ras-driven tumors. Cancer Cell 2011;20:400-13.
-
(2011)
Cancer Cell
, vol.20
, pp. 400-413
-
-
de Raedt, T.1
Walton, Z.2
Yecies, J.L.3
Li, D.4
Chen, Y.5
Malone, C.F.6
-
32
-
-
84873809147
-
MEK inhibition exhibits efficacy in human and mouse neurofibromatosis tumors
-
Jessen WJ, Miller SJ, Jousma E, Wu J, Rizvi TA, Brundage ME, et al. MEK inhibition exhibits efficacy in human and mouse neurofibromatosis tumors. J Clin Invest 2013;123:340-7.
-
(2013)
J Clin Invest
, vol.123
, pp. 340-347
-
-
Jessen, W.J.1
Miller, S.J.2
Jousma, E.3
Wu, J.4
Rizvi, T.A.5
Brundage, M.E.6
-
33
-
-
84873844410
-
Sustained MEK inhibition abrogates myeloproliferative disease in Nf1 mutant mice
-
Chang T, Krisman K, Theobald EH, Xu J, Akutagawa J, Lauchle JO, et al. Sustained MEK inhibition abrogates myeloproliferative disease in Nf1 mutant mice. J Clin Invest 2013;123:335-9.
-
(2013)
J Clin Invest
, vol.123
, pp. 335-339
-
-
Chang, T.1
Krisman, K.2
Theobald, E.H.3
Xu, J.4
Akutagawa, J.5
Lauchle, J.O.6
-
34
-
-
30044432434
-
Hypoxia-inducible factor determines sensitivity to inhibitors of mTOR in kidney cancer
-
Thomas GV, Tran C, Mellinghoff IK, Welsbie DS, Chan E, Fueger B, et al. Hypoxia-inducible factor determines sensitivity to inhibitors of mTOR in kidney cancer. Nat Med 2006;12:122-7.
-
(2006)
Nat Med
, vol.12
, pp. 122-127
-
-
Thomas, G.V.1
Tran, C.2
Mellinghoff, I.K.3
Welsbie, D.S.4
Chan, E.5
Fueger, B.6
-
35
-
-
67650480092
-
mTOR and HIF-1alpha-mediated tumor metabolism in an LKB1 mouse model of Peutz-Jeghers syndrome
-
Shackelford DB, Vasquez DS, Corbeil J, Wu S, Leblanc M, Wu C-L, et al. mTOR and HIF-1alpha-mediated tumor metabolism in an LKB1 mouse model of Peutz-Jeghers syndrome. Proc Natl Acad Sci U S A 2009;106:11137-42.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 11137-11142
-
-
Shackelford, D.B.1
Vasquez, D.S.2
Corbeil, J.3
Wu, S.4
Leblanc, M.5
Wu, C.-L.6
-
36
-
-
65349095566
-
GLUT1 expression is increased in hepatocellular carcinoma and promotes tumorigenesis
-
Amann T, Maegdefrau U, Hartmann A, Agaimy A, Marienhagen J, Weiss TS, et al. GLUT1 expression is increased in hepatocellular carcinoma and promotes tumorigenesis. Am J Pathol 2009;174: 1544-52.
-
(2009)
Am J Pathol
, vol.174
, pp. 1544-1552
-
-
Amann, T.1
Maegdefrau, U.2
Hartmann, A.3
Agaimy, A.4
Marienhagen, J.5
Weiss, T.S.6
-
37
-
-
0030923782
-
Human erythrocyte glucose transporter (Glut1) is immunohistochemically detected as a late event during malignant progression in Barrett's metaplasia
-
Younes M, Ertan A, Lechago LV, Somoano J, Lechago J. Human erythrocyte glucose transporter (Glut1) is immunohistochemically detected as a late event during malignant progression in Barrett's metaplasia. Cancer Epidemiol Biomarkers Prev 1997;6:303-5.
-
(1997)
Cancer Epidemiol Biomarkers Prev
, vol.6
, pp. 303-305
-
-
Younes, M.1
Ertan, A.2
Lechago, L.V.3
Somoano, J.4
Lechago, J.5
-
38
-
-
0035130377
-
Glut1 expression in T1 and T2 stage colorectal carcinomas: Its relationship to clinicopathological features
-
Sakashita M, Aoyama N, Minami R, Maekawa S, Kuroda K, Shirasaka D, et al. Glut1 expression in T1 and T2 stage colorectal carcinomas: its relationship to clinicopathological features. Eur J Cancer 2001;37:204-9.
-
(2001)
Eur J Cancer
, vol.37
, pp. 204-209
-
-
Sakashita, M.1
Aoyama, N.2
Minami, R.3
Maekawa, S.4
Kuroda, K.5
Shirasaka, D.6
-
39
-
-
0031825144
-
Role for glucose transporter 1 protein in human breast cancer
-
Grover-McKay M, Walsh SA, Seftor EA, Thomas PA, Hendrix M.J. Role for glucose transporter 1 protein in human breast cancer. Pathol Oncol Res 1998;4:115-20.
-
(1998)
Pathol Oncol Res
, vol.4
, pp. 115-120
-
-
Grover-McKay, M.1
Walsh, S.A.2
Seftor, E.A.3
Thomas, P.A.4
Hendrix, M.J.5
-
40
-
-
0018938136
-
A fluorinated glucose analog, 2-fluoro-2-deoxy-Dglucose (F-18): Nontoxic tracer for rapid tumor detection
-
Som P, Atkins HL, Bandoypadhyay D, Fowler JS, MacGregor RR, Matsui K, et al. A fluorinated glucose analog, 2-fluoro-2-deoxy-Dglucose (F-18): nontoxic tracer for rapid tumor detection. J Nucl Med 1980;21:670-5.
-
(1980)
J Nucl Med
, vol.21
, pp. 670-675
-
-
Som, P.1
Atkins, H.L.2
Bandoypadhyay, D.3
Fowler, J.S.4
Macgregor, R.R.5
Matsui, K.6
-
41
-
-
0035131831
-
The rate-limiting step for tumor [18F]fluoro-2-deoxy-Dglucose (FDG) incorporation
-
Smith T.A. The rate-limiting step for tumor [18F]fluoro-2-deoxy-Dglucose (FDG) incorporation. Nucl Med Biol 2001;28:1-4.
-
(2001)
Nucl Med Biol
, vol.28
, pp. 1-4
-
-
Smith, T.A.1
-
42
-
-
3242676299
-
GLUT1 expression in tissue and (18)F-FDG uptake
-
Avril N. GLUT1 expression in tissue and (18)F-FDG uptake. J Nucl Med 2004;45:930-2.
-
(2004)
J Nucl Med
, vol.45
, pp. 930-932
-
-
Avril, N.1
-
43
-
-
75649094902
-
Quantitative F18-fluorodeoxyglucose positron emission tomography accurately characterizes peripheral nerve sheath tumors as malignant or benign
-
Benz MR, Czernin J, Dry SM, Tap WD, Allen-Auerbach MS, Elashoff D, et al. Quantitative F18-fluorodeoxyglucose positron emission tomography accurately characterizes peripheral nerve sheath tumors as malignant or benign. Cancer 2010;116:451-8.
-
(2010)
Cancer
, vol.116
, pp. 451-458
-
-
Benz, M.R.1
Czernin, J.2
Dry, S.M.3
Tap, W.D.4
Allen-Auerbach, M.S.5
Elashoff, D.6
-
44
-
-
0030772117
-
Overexpression of Glut1 and Glut3 in stage I nonsmall cell lung carcinoma is associated with poor survival
-
Younes M, Brown RW, Stephenson M, Gondo M, Cagle P.T. Overexpression of Glut1 and Glut3 in stage I nonsmall cell lung carcinoma is associated with poor survival. Cancer 1997;80:1046-51.
-
(1997)
Cancer
, vol.80
, pp. 1046-1051
-
-
Younes, M.1
Brown, R.W.2
Stephenson, M.3
Gondo, M.4
Cagle, P.T.5
-
45
-
-
0031978209
-
Expression of facilitative glucose transporter isoforms in lung carcinomas: Its relation to histologic type, differentiation grade, and tumor stage
-
Ito T, Noguchi Y, Satoh S, Hayashi H, Inayama Y, Kitamura H. Expression of facilitative glucose transporter isoforms in lung carcinomas: its relation to histologic type, differentiation grade, and tumor stage. Mod Pathol 1998;11:437-43.
-
(1998)
Mod Pathol
, vol.11
, pp. 437-443
-
-
Ito, T.1
Noguchi, Y.2
Satoh, S.3
Hayashi, H.4
Inayama, Y.5
Kitamura, H.6
-
46
-
-
0033568454
-
Glut-1 and hexokinase expression: Relationship with 2-fluoro-2-deoxy-D-glucose uptake in A431 and T47D cells in culture
-
Aloj L, Caracó C, Jagoda E, Eckelman WC, Neumann R.D. Glut-1 and hexokinase expression: relationship with 2-fluoro-2-deoxy-D-glucose uptake in A431 and T47D cells in culture. Cancer Res 1999;59:4709-14.
-
(1999)
Cancer Res
, vol.59
, pp. 4709-4714
-
-
Aloj, L.1
Caracó, C.2
Jagoda, E.3
Eckelman, W.C.4
Neumann, R.D.5
-
48
-
-
77949766280
-
Phase I pharmacokinetic and pharmacodynamic study of the oral MAPK/ERK kinase inhibitor PD-0325901 in patients with advanced cancers
-
LoRusso PM, Krishnamurthi SS, Rinehart JJ, Nabell LM, Malburg L, Chapman PB, et al. Phase I pharmacokinetic and pharmacodynamic study of the oral MAPK/ERK kinase inhibitor PD-0325901 in patients with advanced cancers. Clin Cancer Res 2010;16:1924-37.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 1924-1937
-
-
Lorusso, P.M.1
Krishnamurthi, S.S.2
Rinehart, J.J.3
Nabell, L.M.4
Malburg, L.5
Chapman, P.B.6
-
49
-
-
84866623276
-
Ocular toxicity of targeted therapies
-
Renouf DJ, Velazquez-Martin JP, Simpson R, Siu LL, Bedard P.L. Ocular toxicity of targeted therapies. J Clin Oncol 2012;30: 3277-86.
-
(2012)
J Clin Oncol
, vol.30
, pp. 3277-3286
-
-
Renouf, D.J.1
Velazquez-Martin, J.P.2
Simpson, R.3
Siu, L.L.4
Bedard, P.L.5
-
50
-
-
45849110311
-
Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: Effects on mTORC1 and Akt signaling lead to improved survival and function
-
Meikle L, Pollizzi K, Egnor A, Kramvis I, Lane H, Sahin M, et al. Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: effects on mTORC1 and Akt signaling lead to improved survival and function. J Neurosci 2008;28:5422-32.
-
(2008)
J Neurosci
, vol.28
, pp. 5422-5432
-
-
Meikle, L.1
Pollizzi, K.2
Egnor, A.3
Kramvis, I.4
Lane, H.5
Sahin, M.6
-
51
-
-
84890806945
-
Everolimus treatment of refractory epilepsy in tuberous sclerosis complex
-
Krueger DA, Wilfong AA, Holland-Bouley K, Anderson AE, Agricola K, Tudor C, et al. Everolimus treatment of refractory epilepsy in tuberous sclerosis complex. Ann Neurol 2013;74:679-87.
-
(2013)
Ann Neurol
, vol.74
, pp. 679-687
-
-
Krueger, D.A.1
Wilfong, A.A.2
Holland-Bouley, K.3
Anderson, A.E.4
Agricola, K.5
Tudor, C.6
-
52
-
-
84872088946
-
Efficacy and safety of everolimus for subependymal giant cell astrocytomas associated with tuberous sclerosis complex (EXIST-1): A multicentre, randomised, placebo-controlled phase 3 trial
-
Franz DN, Belousova E, Sparagana S, Bebin EM, Frost M, Kuperman R, et al. Efficacy and safety of everolimus for subependymal giant cell astrocytomas associated with tuberous sclerosis complex (EXIST-1): a multicentre, randomised, placebo-controlled phase 3 trial. Lancet 2013;381:125-32.
-
(2013)
Lancet
, vol.381
, pp. 125-132
-
-
Franz, D.N.1
Belousova, E.2
Sparagana, S.3
Bebin, E.M.4
Frost, M.5
Kuperman, R.6
-
53
-
-
84882833554
-
The efficacy and safety of low-dose sirolimus for treatment of lymphangioleiomyomatosis
-
Ando K, Kurihara M, Kataoka H, Ueyama M, Togo S, Sato T, et al. The efficacy and safety of low-dose sirolimus for treatment of lymphangioleiomyomatosis. Respir Investig 2013;51:175-83.
-
(2013)
Respir Investig
, vol.51
, pp. 175-183
-
-
Ando, K.1
Kurihara, M.2
Kataoka, H.3
Ueyama, M.4
Togo, S.5
Sato, T.6
-
54
-
-
33847095086
-
Pharmacodynamic and toxicokinetic evaluation of the novel MEK inhibitor, PD0325901, in the rat following oral and intravenous administration
-
Brown AP, Carlson TCG, Loi C-M, Graziano M.J. Pharmacodynamic and toxicokinetic evaluation of the novel MEK inhibitor, PD0325901, in the rat following oral and intravenous administration. Cancer Chemother Pharmacol 2007;59:671-9.
-
(2007)
Cancer Chemother Pharmacol
, vol.59
, pp. 671-679
-
-
Brown, A.P.1
Carlson, T.C.G.2
Loi, C.-M.3
Graziano, M.J.4
-
55
-
-
84863925300
-
GDC-0941, a novel class I selective PI3K inhibitor, enhances the efficacy of docetaxel in human breast cancer models by increasing cell death in vitro and in vivo
-
Wallin JJ, Guan J, Prior WW, Lee LB, Berry L, Belmont LD, et al. GDC-0941, a novel class I selective PI3K inhibitor, enhances the efficacy of docetaxel in human breast cancer models by increasing cell death in vitro and in vivo. Clin Cancer Res 2012;18:3901-11.
-
(2012)
Clin Cancer Res
, vol.18
, pp. 3901-3911
-
-
Wallin, J.J.1
Guan, J.2
Prior, W.W.3
Lee, L.B.4
Berry, L.5
Belmont, L.D.6
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