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Refinado por: Base de dados/Biblioteca: EZB Electronic Journals Library remover
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1
9-ING-41, a clinically relevant inhibitor of glycogen synthase kinase-3 (GSK-3), is active pre-clinically in human bladder and renal cell cancers
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9-ING-41, a clinically relevant inhibitor of glycogen synthase kinase-3 (GSK-3), is active pre-clinically in human bladder and renal cell cancers

Kuroki, H. ; Anraku, T. ; Bilim, V. ; Tasaki, M. ; Schmitt, D. ; Mazar, A. ; Ugolkov, A. ; Tomita, Y.

Annals of oncology, 2018-10, Vol.29, p.viii9-viii9 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Phase 1 trial of the antiangiogenic peptide ATN-161 (Ac-PHSCN-NH ), a beta integrin antagonist, in patients with solid tumours
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Phase 1 trial of the antiangiogenic peptide ATN-161 (Ac-PHSCN-NH ), a beta integrin antagonist, in patients with solid tumours

Cianfrocca, M E ; Kimmel, K A ; Gallo, J ; Cardoso, T ; Brown, M M ; Hudes, G ; Lewis, N ; Weiner, L ; Lam, G N ; Brown, S C ; Shaw, D E ; Mazar, A P ; Cohen, R B

British journal of cancer, 2006-06, Vol.94 (11), p.1621-1626 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Identification of biomarkers for the antiangiogenic and antitumour activity of the superoxide dismutase 1 (SOD1) inhibitor tetrathiomolybdate (ATN-224)
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Identification of biomarkers for the antiangiogenic and antitumour activity of the superoxide dismutase 1 (SOD1) inhibitor tetrathiomolybdate (ATN-224)

Doñate, F ; Juarez, J C ; Burnett, M E ; Manuia, M M ; Guan, X ; Shaw, D E ; Smith, E L P ; Timucin, C ; Braunstein, M J ; Batuman, O A ; Mazar, A P

British journal of cancer, 2008-02, Vol.98 (4), p.776-783 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Binding of high molecular weight kininogen to human endothelial cells is mediated via a site within domains 2 and 3 of the urokinase receptor
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Binding of high molecular weight kininogen to human endothelial cells is mediated via a site within domains 2 and 3 of the urokinase receptor

Colman, R W ; Pixley, R A ; Najamunnisa, S ; Yan, W ; Wang, J ; Mazar, A ; McCrae, K R

The Journal of clinical investigation, 1997-09, Vol.100 (6), p.1481-1487 [Periódico revisado por pares]

United States

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5
Urokinase-type Plasminogen Activator Receptor (CD87) Is a Ligand for Integrins and Mediates Cell-Cell Interaction
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Urokinase-type Plasminogen Activator Receptor (CD87) Is a Ligand for Integrins and Mediates Cell-Cell Interaction

Tarui, Takehiko ; Mazar, Andrew P. ; Cines, Douglas B. ; Takada, Yoshikazu

The Journal of biological chemistry, 2001-02, Vol.276 (6), p.3983-3990 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Structural requirements for the growth factor activity of the amino-terminal domain of urokinase
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Structural requirements for the growth factor activity of the amino-terminal domain of urokinase

RABBANI, SA ; MAZAR, AP ; BERNIER, SM ; HAQ, M ; BOLIVAR ; HENKIN, J ; GOLTZMAN, D

The Journal of biological chemistry, 1992-07, Vol.267 (20), p.14151-14156 [Periódico revisado por pares]

BETHESDA: American Society for Biochemistry and Molecular Biology

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7
Stimulation of urokinase-type plasminogen activator receptor expression by PMA requires JNK1-dependent and -independent signaling modules
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Stimulation of urokinase-type plasminogen activator receptor expression by PMA requires JNK1-dependent and -independent signaling modules

GUM, R ; JUAREZ, J ; ALLGAYER, H ; MAZAR, A ; WANG, Y ; BOYD, D

Oncogene, 1998-07, Vol.17 (2), p.213-225 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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8
Crystallization of soluble urokinase receptor (suPAR) in complex with urokinase amino-terminal fragment (1-143)
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Crystallization of soluble urokinase receptor (suPAR) in complex with urokinase amino-terminal fragment (1-143)

Huang, Mingdong ; Mazar, Andrew P. ; Parry, Graham ; Higazi, Abd Al-Roof ; Kuo, Alice ; Cines, Douglas B.

Acta crystallographica. Section D, Biological crystallography., 2005-06, Vol.61 (6), p.697-700 [Periódico revisado por pares]

5 Abbey Square, Chester, Cheshire CH1 2HU, England: Munksgaard International Publishers

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9
A Peptide Derived from the Non-Receptor-Binding Region of Urokinase Plasminogen Activator Inhibits Glioblastoma Growth and Angiogenesis in vivo in Combination with Cisplatin
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A Peptide Derived from the Non-Receptor-Binding Region of Urokinase Plasminogen Activator Inhibits Glioblastoma Growth and Angiogenesis in vivo in Combination with Cisplatin

Mishima, Kazuhiko ; Mazar, Andrew P. ; Gown, Allen ; Skelly, Marilyn ; Ji, Xiang-Dong ; Wang, Xu-Dong ; Jones, Terence R. ; Cavenee, Webster K. ; H.-J. Su Huang

Proceedings of the National Academy of Sciences - PNAS, 2000-07, Vol.97 (15), p.8484-8489 [Periódico revisado por pares]

United States: National Academy of Sciences of the United States of America

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10
Novel Interactions between Urokinase and Its Receptor
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Novel Interactions between Urokinase and Its Receptor

Shliom, Ori ; Huang, Mingdong ; Sachais, Bruce ; Kuo, Alice ; Weisel, John W. ; Nagaswami, Chandrasekaran ; Nassar, Taher ; Bdeir, Khalil ; Hiss, Edna ; Gawlak, Susan ; Harris, Scott ; Mazar, Andrew ; Higazi, Abd Al-Roof

The Journal of biological chemistry, 2000-08, Vol.275 (32), p.24304-24312 [Periódico revisado por pares]

United States: Elsevier Inc

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