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Cell Death and Differentiation
|
May 25, 2022
The mitochondrial chaperone TRAP1 regulates F-ATP synthase channel formation
Giuseppe Cannino, Andrea Urbani, Marco Gaspari, et al.
Plos Neglected Tropical Diseases
|
July 30, 2015
Sequence- and Structure-Based Immunoreactive Epitope Discovery for Burkholderia pseudomallei Flagellin
Arnone Nithichanon, Darawan Rinchai, Alessandro Gori, et al.
Communications Medicine
|
March 5, 2026
Spatial navigation as a digital marker for clinically differentiating cognitive impairment severity
Giorgio Colombo, Karolina Minta, William R Taylor, et al.
ACS Infectious Diseases
|
March 24, 2018
Enhancing Antibody Serodiagnosis Using a Controlled Peptide Coimmobilization Strategy
Laura Sola, Paola Gagni, Ilda D'Annessa, et al.
Chemical Science
|
June 14, 2021
Tryptophan scanning mutagenesis as a way to mimic the compound-bound state and probe the selectivity of allosteric inhibitors in cells
Isabelle R Taylor, Victoria A Assimon, Szu Yu Kuo, et al.
Cancer Cell
|
August 13, 2015
Long-Pentraxin 3 Derivative as a Small-Molecule FGF Trap for Cancer Therapy
Roberto Ronca, Arianna Giacomini, Emanuela Di Salle, et al.
Angiogenesis
|
September 1, 2018
The calcium-binding type III repeats domain of thrombospondin-2 binds to fibroblast growth factor 2 (FGF2)
Marco Rusnati, Patrizia Borsotti, Elisabetta Moroni, et al.
The Journal of Biological Chemistry
|
January 9, 2010
Non-peptidic thrombospondin-1 mimics as fibroblast growth factor-2 inhibitors: an integrated strategy for the development of new antiangiogenic compounds
Giorgio Colombo, Barbara Margosio, Laura Ragona, et al.
Redox Biology
|
May 27, 2025
Disulfide-mediated tetramerization of TRAP1 fosters its antioxidant and pro-neoplastic activities
Fiorella Faienza, Claudio Laquatra, Matteo Castelli, et al.
Journal of Medicinal Chemistry
|
February 19, 2020
Dual Binding to Orthosteric and Allosteric Sites Enhances the Anticancer Activity of a TRAP1-Targeting Drug
Sung Hu, Mariarosaria Ferraro, Ajesh P Thomas, et al.
Page
of 28
Search research articles
Search
Showing results (251-260 of 280) with videos related to
Sort By:
Page
of 28
Cell Death and Differentiation
|
May 25, 2022
The mitochondrial chaperone TRAP1 regulates F-ATP synthase channel formation
Giuseppe Cannino, Andrea Urbani, Marco Gaspari, et al.
Plos Neglected Tropical Diseases
|
July 30, 2015
Sequence- and Structure-Based Immunoreactive Epitope Discovery for Burkholderia pseudomallei Flagellin
Arnone Nithichanon, Darawan Rinchai, Alessandro Gori, et al.
Communications Medicine
|
March 5, 2026
Spatial navigation as a digital marker for clinically differentiating cognitive impairment severity
Giorgio Colombo, Karolina Minta, William R Taylor, et al.
ACS Infectious Diseases
|
March 24, 2018
Enhancing Antibody Serodiagnosis Using a Controlled Peptide Coimmobilization Strategy
Laura Sola, Paola Gagni, Ilda D'Annessa, et al.
Chemical Science
|
June 14, 2021
Tryptophan scanning mutagenesis as a way to mimic the compound-bound state and probe the selectivity of allosteric inhibitors in cells
Isabelle R Taylor, Victoria A Assimon, Szu Yu Kuo, et al.
Cancer Cell
|
August 13, 2015
Long-Pentraxin 3 Derivative as a Small-Molecule FGF Trap for Cancer Therapy
Roberto Ronca, Arianna Giacomini, Emanuela Di Salle, et al.
Angiogenesis
|
September 1, 2018
The calcium-binding type III repeats domain of thrombospondin-2 binds to fibroblast growth factor 2 (FGF2)
Marco Rusnati, Patrizia Borsotti, Elisabetta Moroni, et al.
The Journal of Biological Chemistry
|
January 9, 2010
Non-peptidic thrombospondin-1 mimics as fibroblast growth factor-2 inhibitors: an integrated strategy for the development of new antiangiogenic compounds
Giorgio Colombo, Barbara Margosio, Laura Ragona, et al.
Redox Biology
|
May 27, 2025
Disulfide-mediated tetramerization of TRAP1 fosters its antioxidant and pro-neoplastic activities
Fiorella Faienza, Claudio Laquatra, Matteo Castelli, et al.
Journal of Medicinal Chemistry
|
February 19, 2020
Dual Binding to Orthosteric and Allosteric Sites Enhances the Anticancer Activity of a TRAP1-Targeting Drug
Sung Hu, Mariarosaria Ferraro, Ajesh P Thomas, et al.
Page
of 28