-
1
-
-
0026580592
-
Effect of a single amino acid mutation on the activating and immunosuppressive properties of a "humanized" OKT3 monoclonal antibody
-
Alegre, ML, AM Collins, VL Pulito, RA Brosius, WC Olson, RA Zivin, R Knowles, JR Thistlethwaite, LK Jolliffe, and JA Bluestone (1992). Effect of a single amino acid mutation on the activating and immunosuppressive properties of a "humanized" OKT3 monoclonal antibody. J Immunol, 148, 3461-68.
-
(1992)
J Immunol
, vol.148
, pp. 3461-68
-
-
Alegre, M.L.1
Collins, A.M.2
Pulito, V.L.3
Brosius, R.A.4
Olson, W.C.5
Zivin, R.A.6
Knowles, R.7
Thistlethwaite, J.R.8
Jolliffe, L.K.9
Bluestone, J.A.10
-
2
-
-
0024989373
-
Acute toxicity of anti-CD3 monoclonal antibody in mice: A model for OKT3 first dose reactions
-
Alegre, ML, M Depierreux, S Florquin, T Najdovski, P Vandenabeele, D Abramowicz, O Leo, M Deschodt-Lanckman, and M Goldman (1990). Acute toxicity of anti-CD3 monoclonal antibody in mice: A model for OKT3 first dose reactions. Transplant Proc, 22, 1920-21.
-
(1990)
Transplant Proc
, vol.22
, pp. 1920-21
-
-
Alegre, M.L.1
Depierreux, M.2
Florquin, S.3
Najdovski, T.4
Vandenabeele, P.5
Abramowicz, D.6
Leo, O.7
Deschodt-Lanckman, M.8
Goldman, M.9
-
3
-
-
68649129160
-
-
Association of the British Pharmaceutical Industry and BioIndustry Association (APBI/BIA) London.
-
Association of the British Pharmaceutical Industry and BioIndustry Association (APBI/BIA) (1977). Guidelines for preclinical testing on new medicinal products. Parts 1 and 2. London.
-
(1977)
Guidelines for Preclinical Testing on New Medicinal Products. Parts 1 and 2
-
-
-
5
-
-
28744450284
-
CD28 superagonists put a break on autoimmunity by preferentially activating CD4+CD25+ regulatory T cells
-
Beyersdorf, N, T Hanke, T Kerkau, and T Hünig (2006). CD28 superagonists put a break on autoimmunity by preferentially activating CD4+CD25+ regulatory T cells. Autoimmun Rev, 5, 40-45.
-
(2006)
Autoimmun Rev
, vol.5
, pp. 40-45
-
-
Beyersdorf, N.1
Hanke, T.2
Kerkau, T.3
Hünig, T.4
-
6
-
-
68649109477
-
Cytokine release assays: Current approaches and considerations
-
BioSafe General Membership Meeting, Cambridge, MA
-
BioSafe General Membership Meeting (2008). Cytokine release assays: Current approaches and considerations. In Cytokine release assays: Current approaches and considerations. Cambridge, MA.
-
(2008)
Cytokine Release Assays: Current Approaches and Considerations
-
-
-
7
-
-
0025639047
-
In vivo use of OKT3: Main issues for the monitoring of treated patients
-
Chatenoud, L, C Ferran, and JF Bach (1990). In vivo use of OKT3: Main issues for the monitoring of treated patients. Transplant Proc, 22, 2605-8.
-
(1990)
Transplant Proc
, vol.22
, pp. 2605-8
-
-
Chatenoud, L.1
Ferran, C.2
Bach, J.F.3
-
8
-
-
0032880425
-
HuM291, a humanized anti-CD3 antibody, is immunosuppressive to T cells while exhibiting reduced mitogenicity in vitro
-
Cole, MS, KE Stellrecht, JD Shi, M Homola, DH Hsu, C Anasetti, M Vasquez, and JY Tso (1999). HuM291, a humanized anti-CD3 antibody, is immunosuppressive to T cells while exhibiting reduced mitogenicity in vitro. Transplantation, 68, 563-71.
-
(1999)
Transplantation
, vol.68
, pp. 563-71
-
-
Cole, M.S.1
Stellrecht, K.E.2
Shi, J.D.3
Homola, M.4
Hsu, D.H.5
Anasetti, C.6
Vasquez, M.7
Tso, J.Y.8
-
9
-
-
14444267319
-
Regulatory considerations for pre-clinical development of anticancer drugs
-
DeGeorge, JJ, CH Ahn, PA Andrews, ME Brower, DW Giorgio, MA Goheer, DY Lee-Ham, WD McGuinn, W Schmidt, CJ Sun, and SC Tripathi (1997). Regulatory considerations for pre-clinical development of anticancer drugs. Cancer Chemother Pharmacol, 41, 173-85.
-
(1997)
Cancer Chemother Pharmacol
, vol.41
, pp. 173-85
-
-
Degeorge, J.J.1
Ahn, C.2
Andrews, P.A.3
Brower, M.E.4
Giorgio, D.W.5
Goheer, M.6
Lee-Ham, D.Y.7
McGuinn, W.D.8
Schmidt, W.9
Sun, C.J.10
Tripathi, S.C.11
-
10
-
-
68649101678
-
-
Early Stage Clinical Trial Taskforce Early Stage Clinical Trial Taskforce Association of the British Pharmaceutical Industry and BioIndustry Association.
-
Early Stage Clinical Trial Taskforce (2007). Early Stage Clinical Trial Taskforce-Joint ABPI/BIA report. Association of the British Pharmaceutical Industry and BioIndustry Association.
-
(2007)
-
-
-
14
-
-
68649109943
-
Cytokine release: What does it mean to you?
-
FDA CDER Immunotoxicology Subcommittee Meeting Rockville, MD: FDA White Oak Campus.
-
FDA CDER Immunotoxicology Subcommittee Meeting (2008). Cytokine release: What does it mean to you?. In Cytokine release: What does it mean to you?. Rockville, MD: FDA White Oak Campus.
-
(2008)
Cytokine Release: What Does It Mean to You?
-
-
-
15
-
-
38849130659
-
-
FDA Science Board, Subcommittee on Science and Technology Washington, DC.
-
FDA Science Board, Subcommittee on Science and Technology (2007). FDA science and mission at risk. Washington, DC.
-
(2007)
FDA Science and Mission at Risk
-
-
-
16
-
-
68649117982
-
Can EU regulators keep up with innovation?
-
November 8
-
Gambrill, S (November 8, 2006). Can EU regulators keep up with innovation? Clinical Trials Today. http://www.clinicaltrialstoday.com/2006/11/ can-eu-regulato.html. (accessed November 4, 2008).
-
(2006)
Clinical Trials Today
-
-
Gambrill, S.1
-
17
-
-
0026071251
-
OKT3 first-dose reaction: Association with T cell subsets and cytokine release
-
Gaston, RS, MH Deierhoi, T Patterson, E Prasthofer, BA Julian, WH Barber, DA Laskow, AG Diethelm, and JJ Curtis (1991). OKT3 first-dose reaction: association with T cell subsets and cytokine release. Kidney Int, 39 (1). 141-48.
-
(1991)
Kidney Int
, vol.39
, Issue.1
, pp. 141-48
-
-
Gaston, R.S.1
Deierhoi, M.H.2
Patterson, T.3
Prasthofer, E.4
Julian, B.A.5
Barber, W.H.6
Laskow, D.A.7
Diethelm, A.G.8
Curtis, J.J.9
-
18
-
-
68649092117
-
Victim Ryan Wilson in "elephant man" drug trial to get £2m
-
London.
-
Gibb, F (2008). Victim Ryan Wilson in "elephant man" drug trial to get £2m. In The Times. London.
-
(2008)
The Times
-
-
Gibb, F.1
-
19
-
-
1642282158
-
First dose of potential new medicines to humans: How animals help
-
Greaves, P, A Williams, and M Eve (2004). First dose of potential new medicines to humans: How animals help. Nat Rev Drug Discov, 3, 226-36.
-
(2004)
Nat Rev Drug Discov
, vol.3
, pp. 226-36
-
-
Greaves, P.1
Williams, A.2
Eve, M.3
-
20
-
-
0020835433
-
Effects of monoclonal anti-lymphocyte antibodies in vivo in monkeys and humans
-
Hale, G, DM Swirsky, FG Hayhoe, and H Waldmann (1983). Effects of monoclonal anti-lymphocyte antibodies in vivo in monkeys and humans. Mol Biol Med, 1, 321-34.
-
(1983)
Mol Biol Med
, vol.1
, pp. 321-34
-
-
Hale, G.1
Swirsky, D.M.2
Hayhoe, F.G.3
Waldmann, H.4
-
21
-
-
0344604333
-
A humanized anti-CD3 antibody, HuM291, with low mitogenic activity, mediates complete and reversible T-cell depletion in chimpanzees
-
Hsu, DH, JD Shi, M Homola, TJ Rowell, J Moran, D Levitt, B Druilhet, J Chinn, C Bullock, and C Klingbeil (1999). A humanized anti-CD3 antibody, HuM291, with low mitogenic activity, mediates complete and reversible T-cell depletion in chimpanzees. Transplantation, 68, 545-54.
-
(1999)
Transplantation
, vol.68
, pp. 545-54
-
-
Hsu, D.H.1
Shi, J.D.2
Homola, M.3
Rowell, T.J.4
Moran, J.5
Levitt, D.6
Druilhet, B.7
Chinn, J.8
Bullock, C.9
Klingbeil, C.10
-
22
-
-
43349093221
-
Projection of exposure and efficacious dose prior to first-in-human studies: How successful have we been?
-
Huang, C, M Zheng, Z Yang, AD Rodrigues, and P Marathe (2008). Projection of exposure and efficacious dose prior to first-in-human studies: How successful have we been? Pharm Res, 25, 713-26.
-
(2008)
Pharm Res
, vol.25
, pp. 713-26
-
-
Huang, C.1
Zheng, M.2
Yang, Z.3
Rodrigues, A.D.4
Marathe, P.5
-
23
-
-
68649087968
-
International conference on harmonisation of technical requirements for registration of pharmaceuticals for human use (ICH)
-
June 10 Good clinical practice: Consolidated guideline. E6(R1)
-
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) (June 10, 1996). ICH harmonised tripartite guideline. Good clinical practice: Consolidated guideline. E6(R1).. http://www.ich.org/LOB/media/MEDIA482.pdf. (accessed March 6, 2008).
-
(1996)
ICH Harmonised Tripartite Guideline
-
-
-
24
-
-
84928589419
-
International Conference on harmonisation of technical requirements for registration of pharmaceuticals for human use (ICH)
-
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) (1998). ICH harmonised tripartite guideline Statistical principles for clinical trials. E9. http://www.ich.org/LOB/media/MEDIA485.pdf. (accessed March 28, 2008).
-
(1998)
ICH Harmonised Tripartite Guideline Statistical Principles for Clinical Trials. E9
-
-
-
25
-
-
68649107224
-
-
International conference on harmonisation of technical requirements for registration of pharmaceuticals for human use (ICH) November 9 Maintenance of the ICH guideline on non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals. M3(R1)
-
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) (November 9, 2000). ICH harmonised tripartite guideline. Maintenance of the ICH guideline on non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals. M3(R1). http://www.ich.org/LOB/media/MEDIA506.pdf. (accessed March 4, 2008).
-
(2000)
ICH Harmonised Tripartite Guideline
-
-
-
26
-
-
68649124183
-
International conference on harmonisation of technical requirements for registration of pharmaceuticals for human use (ICH)
-
July 15 Guidance on nonclinical safety studies for the conduct of human clinical trials and marketing authorization for pharmaceuticals. M3(R2). Step 2
-
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) (July 15, 2008a). ICH harmonised tripartite guideline. Guidance on nonclinical safety studies for the conduct of human clinical trials and marketing authorization for pharmaceuticals. M3(R2). Step 2. http://www.ich.org/LOB/media/MEDIA4744.pdf. (accessed August 21, 2008).
-
(2008)
ICH Harmonised Tripartite Guideline
-
-
-
27
-
-
68649090847
-
International conference on harmonisation of technical requirements for registration of pharmaceuticals for human use (ICH)
-
Monitoring and Protecting the Global Public Health, May 31-June 5, Portland, Oregon, USA
-
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) (2008b). ICH Steering Committee meeting. Monitoring and Protecting the Global Public Health, May 31-June 5, Portland, Oregon, USA. http://www.ich.org/cache/compo/276-254-1.html. (accessed August 21, 2008).
-
(2008)
ICH Steering Committee Meeting
-
-
-
28
-
-
0032979346
-
Pharmacology and safety assessment of humanized monoclonal antibodies for therapeutic use
-
Klingbeil, C, and DH Hsu (1999). Pharmacology and safety assessment of humanized monoclonal antibodies for therapeutic use. Toxicol Pathol, 27, 1-3.
-
(1999)
Toxicol Pathol
, vol.27
, pp. 1-3
-
-
Klingbeil, C.1
Hsu, D.H.2
-
29
-
-
33745604934
-
Transient accumulation of human mature thymocytes and regulatory T cells with CD28 superagonist in "human immune system" Rag2(/)gammac(/) mice
-
Legrand, N, T Cupedo, AU van Lent, MJ Ebeli, K Weijer, T Hanke, and H Spits (2006). Transient accumulation of human mature thymocytes and regulatory T cells with CD28 superagonist in "human immune system" Rag2(/)gammac(/) mice. Blood, 108, 238-45.
-
(2006)
Blood
, vol.108
, pp. 238-45
-
-
Legrand, N.1
Cupedo, T.2
Van Lent, A.U.3
Ebeli, M.J.4
Weijer, K.5
Hanke, T.6
Spits, H.7
-
30
-
-
33847375862
-
Safety of Phase i clinical trials with monoclonal antibodies in Germany - The regulatory requirements viewed in the aftermath of the TGN1412 disaster
-
Liedert, B, S Bassus, CK Schneider, U Kalinke, and J Lower (2007). Safety of Phase I clinical trials with monoclonal antibodies in Germany - The regulatory requirements viewed in the aftermath of the TGN1412 disaster. Intl J Clin Pharm Thera, 45, 1-9.
-
(2007)
Intl J Clin Pharm Thera
, vol.45
, pp. 1-9
-
-
Liedert, B.1
Bassus, S.2
Schneider, C.K.3
Kalinke, U.4
Lower, J.5
-
31
-
-
0037352740
-
Efficient expansion of regulatory T cells in vitro and in vivo with a CD28 superagonist
-
Lin, CH, and T Hunig (2003). Efficient expansion of regulatory T cells in vitro and in vivo with a CD28 superagonist. Eur J Immunol, 33, 626-38.
-
(2003)
Eur J Immunol
, vol.33
, pp. 626-38
-
-
Lin, C.H.1
Hunig, T.2
-
32
-
-
35648945837
-
On the anticipation of the human dose in first-in-man trials from preclinical and prior clinical information in early drug development
-
Lowe, PJ (2007). On the anticipation of the human dose in first-in-man trials from preclinical and prior clinical information in early drug development. Xenobiotica, 37, 1331-54.
-
(2007)
Xenobiotica
, vol.37
, pp. 1331-54
-
-
Lowe, P.J.1
-
33
-
-
0042505740
-
Topological requirements and signaling properties of T cell-activating, anti-CD28 antibody superagonists
-
Lühder, F, Y Huang, KM Dennehy, C Guntermann, I Müller, E Winkler, T Kerkau, S Ikemizu, SJ Davis, T Hanke, and T Hünig (2003). Topological requirements and signaling properties of T cell-activating, anti-CD28 antibody superagonists. J Exp Med, 197, 955-66.
-
(2003)
J Exp Med
, vol.197
, pp. 955-66
-
-
Lühder, F.1
Huang, Y.2
Dennehy, K.M.3
Guntermann, C.4
Müller, I.5
Winkler, E.6
Kerkau, T.7
Ikemizu, S.8
Davis, S.J.9
Hanke, T.10
Hünig, T.11
-
34
-
-
20344382965
-
The correction factors do help in improving the prediction of human clearance from animal data
-
Mahmood, I (2005). The correction factors do help in improving the prediction of human clearance from animal data. J Pharm Sci, 94, 940-45.
-
(2005)
J Pharm Sci
, vol.94
, pp. 940-45
-
-
Mahmood, I.1
-
35
-
-
84872496267
-
-
Medicines and Healthcare Products Regulatory Agency (MHRA) (April 5)
-
Medicines and Healthcare Products Regulatory Agency (MHRA) (April 5, 2006a). Clinical trial suspension: Latest findings. http://www.mhra.gov.uk/ NewsCentre/Pressreleases/CON2023515. (accessed March 26, 2008).
-
(2006)
Clinical Trial Suspension: Latest Findings
-
-
-
37
-
-
67049107949
-
The EMEA guideline on first-inhuman clinical trials and its impact on pharmaceutical development
-
Milton, MN, and CJ Horvath (2009). The EMEA guideline on first-inhuman clinical trials and its impact on pharmaceutical development. Toxicol Pathol, 37, 363-371.
-
(2009)
Toxicol Pathol
, vol.37
, pp. 363-371
-
-
Milton, M.N.1
Horvath, C.J.2
-
38
-
-
41849146099
-
A CD28 superagonistic antibody elicits 2 functionally distinct waves of T cell activation in rats
-
Müller, N, J van den Brandt, F Odoardi, D Tischner, J Herath, A Flügel, and HM Reichardt (2008). A CD28 superagonistic antibody elicits 2 functionally distinct waves of T cell activation in rats. J Clin Invest, 118, 1405-16.
-
(2008)
J Clin Invest
, vol.118
, pp. 1405-16
-
-
Müller, N.1
Brandt Den J.Van2
Odoardi, F.3
Tischner, D.4
Herath, J.5
Flügel, A.6
Reichardt, H.M.7
-
39
-
-
4844222525
-
A comprehensive analysis of the role of correction factors in the allometric predictivity of clearance from rat, dog, and monkey to humans
-
Nagilla, R, and KW Ward (2004). A comprehensive analysis of the role of correction factors in the allometric predictivity of clearance from rat, dog, and monkey to humans. J Pharm Sci, 93, 2522-34.
-
(2004)
J Pharm Sci
, vol.93
, pp. 2522-34
-
-
Nagilla, R.1
Ward, K.W.2
-
41
-
-
12244274985
-
Erratum: A comprehensive analysis of the role of correction factors in the allometric predictivity of clearance from rat, dog, and monkey to humans
-
Nagilla, R, and KW Ward (2005b). Erratum: A comprehensive analysis of the role of correction factors in the allometric predictivity of clearance from rat, dog, and monkey to humans. J Pharm Sci, 94, 231-32.
-
(2005)
J Pharm Sci
, vol.94
, pp. 231-32
-
-
Nagilla, R.1
Ward, K.W.2
-
42
-
-
33646734488
-
Loss of Siglec expression on T lymphocytes during human evolution
-
Nguyen, DH, N Hurtado-Ziola, P Gagneux, and A Varki (2006). Loss of Siglec expression on T lymphocytes during human evolution. Proc Natl Acad Sci USA, 103, 7765-70.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 7765-70
-
-
Nguyen, D.H.1
Hurtado-Ziola, N.2
Gagneux, P.3
Varki, A.4
-
43
-
-
0034722921
-
Phase i trial of HuM291, a humanized anti-CD3 antibody, in patients receiving renal allografts from living donors
-
Norman, DJ, F Vincenti, AM de Mattos, JM Barry, DJ Levitt, NI Wedel, M Maia, and SE Light (2000). Phase I trial of HuM291, a humanized anti-CD3 antibody, in patients receiving renal allografts from living donors. Transplantation, 70, 1707-12.
-
(2000)
Transplantation
, vol.70
, pp. 1707-12
-
-
Norman, D.J.1
Vincenti, F.2
De Mattos, A.M.3
Barry, J.M.4
Levitt, D.J.5
Wedel, N.I.6
Maia, M.7
Light, S.E.8
-
44
-
-
0025991961
-
OKT3E, an anti-CD3 antibody that does not elicit side effects or antiidiotype responses in chimpanzees
-
Rao, PE, G Olini, J Kille, E Muchmore, MA Talle, G Brake, and SA Rudnick (1991). OKT3E, an anti-CD3 antibody that does not elicit side effects or antiidiotype responses in chimpanzees. Transplantation, 52, 691-97.
-
(1991)
Transplantation
, vol.52
, pp. 691-97
-
-
Rao, P.E.1
Olini, G.2
Kille, J.3
Muchmore, E.4
Talle, M.5
Brake, G.6
Rudnick, S.A.7
-
45
-
-
36148960050
-
Commentary on ACCP position statement on the use of microdosing in the drug development process
-
Rowland, M (2007). Commentary on ACCP position statement on the use of microdosing in the drug development process. J Clin Pharmacol, 47, 1595-96.
-
(2007)
J Clin Pharmacol
, vol.47
, pp. 1595-96
-
-
Rowland, M.1
-
47
-
-
33748750980
-
Regulating biopharmaceuticals under CDER versus CBER: An insider's perspective
-
Schwieterman, W (2006). Regulating biopharmaceuticals under CDER versus CBER: An insider's perspective. Drug Discov Today, 11, 945-51.
-
(2006)
Drug Discov Today
, vol.11
, pp. 945-51
-
-
Schwieterman, W.1
-
48
-
-
52649088433
-
Statistical issues in first-in-man studies
-
Senn, S, D Amin, R Bailey, S Bird, B Bogacka, P Colman, A Garett, A Grieve, and P Lachman (2007). Statistical issues in first-in-man studies. J Royal Stat Soc A, 170, 517-79.
-
(2007)
J Royal Stat Soc A
, vol.170
, pp. 517-79
-
-
Senn, S.1
Amin, D.2
Bailey, R.3
Bird, S.4
Bogacka, B.5
Colman, P.6
Garett, A.7
Grieve, A.8
Lachman, P.9
-
50
-
-
0033648133
-
Phylogenetic variation and polymorphism at the toll-like receptor 4 locus (TLR4)
-
Smirnova, I, A Poltorak, EK Chan, C McBride, and B Beutler (2000). Phylogenetic variation and polymorphism at the toll-like receptor 4 locus (TLR4). Genome Biol, 1, RESEARCH002.
-
(2000)
Genome Biol
, vol.1
, pp. 002
-
-
Smirnova, I.1
Poltorak, A.2
Chan, E.K.3
McBride, C.4
Beutler, B.5
-
51
-
-
41849116016
-
The calm after the cytokine storm: Lessons from the TGN1412 trial
-
St Clair, EW (2008). The calm after the cytokine storm: Lessons from the TGN1412 trial. J Clin Invest, 118, 1344-47.
-
(2008)
J Clin Invest
, vol.118
, pp. 1344-47
-
-
St Clair, E.W.1
-
52
-
-
37749032491
-
"cytokine storm" in the Phase i trial of monoclonal antibody TGN1412: Better understanding the causes to improve pre-clinical testing of immunotherapeutics"
-
Stebbings, R (2007). "Cytokine storm" in the Phase I trial of monoclonal antibody TGN1412: Better understanding the causes to improve pre-clinical testing of immunotherapeutics". J Immunol, 179, 3325-31.
-
(2007)
J Immunol
, vol.179
, pp. 3325-31
-
-
Stebbings, R.1
-
53
-
-
33748416499
-
Cytokine storm in a Phase 1 trial of the anti-CD28 monoclonal antibody TGN1412
-
Suntharalingam, G, MR Perry, S Ward, SJ Brett, A Castello-Cortes, MD Brunner, and N Panoskaltsis (2006). Cytokine storm in a Phase 1 trial of the anti-CD28 monoclonal antibody TGN1412. N Engl J Med, 355, 1018-28.
-
(2006)
N Engl J Med
, vol.355
, pp. 1018-28
-
-
Suntharalingam, G.1
Perry, M.R.2
Ward, S.3
Brett, S.J.4
Castello-Cortes, A.5
Brunner, M.D.6
Panoskaltsis, N.7
-
54
-
-
34447091994
-
Preclinical and clinical safety of monoclonal antibodies
-
Tabrizi, MA, and LK Roskos (2007). Preclinical and clinical safety of monoclonal antibodies. Drug Discov Today, 12 (13-14). 540-47.
-
(2007)
Drug Discov Today
, vol.12
, Issue.1314
, pp. 540-47
-
-
Tabrizi, M.A.1
Roskos, L.K.2
-
55
-
-
0031034123
-
CD28-mediated induction of proliferation in resting T cells in vitro and in vivo without engagement of the T cell receptor: Evidence for functionally distinct forms of CD28
-
Tacke, M, G Hanke, T Hanke, and T Hünig (1997). CD28-mediated induction of proliferation in resting T cells in vitro and in vivo without engagement of the T cell receptor: Evidence for functionally distinct forms of CD28. Eur J Immunol, 27, 239-47.
-
(1997)
Eur J Immunol
, vol.27
, pp. 239-47
-
-
Tacke, M.1
Hanke, G.2
Hanke, T.3
Hünig, T.4
-
59
-
-
0018836897
-
OKT3: A monoclonal anti-human T lymphocyte antibody with potent mitogenic properties
-
Van Wauwe, JP, JR De Mey, and JG Goossens (1980). OKT3: a monoclonal anti-human T lymphocyte antibody with potent mitogenic properties. J Immunol, 124, 2708-13.
-
(1980)
J Immunol
, vol.124
, pp. 2708-13
-
-
Van Wauwe, J.P.1
De Mey, J.R.2
Goossens, J.G.3
-
60
-
-
43049154225
-
Signaling signatures and functional properties of anti-human cd28 superagonistic antibodies
-
Waibler, Z, LY Sender, C Merten, R Hartig, S Kliche, M Gunzer, P Reichardt, U Kalinke, and B Schraven (2008). Signaling signatures and functional properties of anti-human cd28 superagonistic antibodies. PLoS ONE, 3, e1708.
-
(2008)
PLoS ONE
, vol.3
, pp. 1708
-
-
Waibler, Z.1
Sender, L.Y.2
Merten, C.3
Hartig, R.4
Kliche, S.5
Gunzer, M.6
Reichardt, P.7
Kalinke, U.8
Schraven, B.9
-
61
-
-
2442680354
-
A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. I. Clearance
-
Ward, KW, and BR Smith (2004a). A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. I. Clearance. Drug Metab Dispos, 32, 603-11.
-
(2004)
Drug Metab Dispos
, vol.32
, pp. 603-11
-
-
Ward, K.W.1
Smith, B.R.2
-
62
-
-
2442691625
-
A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. II. Volume of distribution and mean residence time
-
Ward, KW, and BR Smith (2004b). A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. II. Volume of distribution and mean residence time. Drug Metab Dispos, 32, 612-19.
-
(2004)
Drug Metab Dispos
, vol.32
, pp. 612-19
-
-
Ward, K.W.1
Smith, B.R.2
-
63
-
-
0030453977
-
Mechanism of first-dose cytokine-release syndrome by CAMPATH 1-H: Involvement of CD16 (FcgammaRIII) and CD11a/CD18 (LFA-1) on NK cells
-
Wing, MG, T Moreau, J Greenwood, RM Smith, G Hale, J Isaacs, H Waldmann, PJ Lachmann, and A Compston (1996). Mechanism of first-dose cytokine-release syndrome by CAMPATH 1-H: involvement of CD16 (FcgammaRIII) and CD11a/CD18 (LFA-1) on NK cells. J Clin Invest, 98, 2819-26.
-
(1996)
J Clin Invest
, vol.98
, pp. 2819-26
-
-
Wing, M.G.1
Moreau, T.2
Greenwood, J.3
Smith, R.M.4
Hale, G.5
Isaacs, J.6
Waldmann, H.7
Lachmann, P.J.8
Compston, A.9
-
64
-
-
0033214207
-
Cytokine-release syndrome in patients with B-cell chronic lymphocytic leukemia and high lymphocyte counts after treatment with an anti-CD20 monoclonal antibody (rituximab, IDEC-C2B8)
-
Winkler, U, M Jensen, O Manzke, H Schulz, V Diehl, and A Engert (1999). Cytokine-release syndrome in patients with B-cell chronic lymphocytic leukemia and high lymphocyte counts after treatment with an anti-CD20 monoclonal antibody (rituximab, IDEC-C2B8). Blood, 94, 2217-24.
-
(1999)
Blood
, vol.94
, pp. 2217-24
-
-
Winkler, U.1
Jensen, M.2
Manzke, O.3
Schulz, H.4
Diehl, V.5
Engert, A.6
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