Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Christophe, Pardin"'
Autor:
Hinrich Gronemeyer, Gilles Guichard, Olivier Micheau, Sylvie Fournel, Wolfgang Maison, Miriam Wendland, Jean-Paul Briand, Marie-Charlotte Lechner, Alexandre Morizot, Christophe Pardin, Julien Beyrath, Valeria Pavet
Supplementary Figure 2 from Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e3c88e6a9615c2e71e63f1bdfc81610
https://doi.org/10.1158/0008-5472.22384586.v1
https://doi.org/10.1158/0008-5472.22384586.v1
Autor:
Hinrich Gronemeyer, Gilles Guichard, Olivier Micheau, Sylvie Fournel, Wolfgang Maison, Miriam Wendland, Jean-Paul Briand, Marie-Charlotte Lechner, Alexandre Morizot, Christophe Pardin, Julien Beyrath, Valeria Pavet
Supplementary Figure 3 from Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5652762e0c75397fb356e96fde3f52d7
https://doi.org/10.1158/0008-5472.22384583.v1
https://doi.org/10.1158/0008-5472.22384583.v1
Autor:
Hinrich Gronemeyer, Gilles Guichard, Olivier Micheau, Sylvie Fournel, Wolfgang Maison, Miriam Wendland, Jean-Paul Briand, Marie-Charlotte Lechner, Alexandre Morizot, Christophe Pardin, Julien Beyrath, Valeria Pavet
Supplementary Figure 5 from Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5491bea60a17fb03e3922e2ede581cc4
https://doi.org/10.1158/0008-5472.22384577.v1
https://doi.org/10.1158/0008-5472.22384577.v1
Autor:
Hinrich Gronemeyer, Gilles Guichard, Olivier Micheau, Sylvie Fournel, Wolfgang Maison, Miriam Wendland, Jean-Paul Briand, Marie-Charlotte Lechner, Alexandre Morizot, Christophe Pardin, Julien Beyrath, Valeria Pavet
Supplementary Figure 1 from Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb44e155f8e413e2c75ef3779475470
https://doi.org/10.1158/0008-5472.22384589
https://doi.org/10.1158/0008-5472.22384589
Autor:
Hinrich Gronemeyer, Gilles Guichard, Olivier Micheau, Sylvie Fournel, Wolfgang Maison, Miriam Wendland, Jean-Paul Briand, Marie-Charlotte Lechner, Alexandre Morizot, Christophe Pardin, Julien Beyrath, Valeria Pavet
Supplementary Figure Legends 1-5 from Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f6bf7aa9930b5250575c75adfafbf3e
https://doi.org/10.1158/0008-5472.22384574.v1
https://doi.org/10.1158/0008-5472.22384574.v1
Autor:
Hinrich Gronemeyer, Gilles Guichard, Olivier Micheau, Sylvie Fournel, Wolfgang Maison, Miriam Wendland, Jean-Paul Briand, Marie-Charlotte Lechner, Alexandre Morizot, Christophe Pardin, Julien Beyrath, Valeria Pavet
Supplementary Figure 4 from Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef35d722cc1f8e33bb68556a875c7847
https://doi.org/10.1158/0008-5472.22384580
https://doi.org/10.1158/0008-5472.22384580
Autor:
Christopher N. Boddy, Christophe Pardin, Atahualpa Pinto, Fabien Bergeret, Panos Argyropoulos, J.M. Reimer, T. Martin Schmeing
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1860:486-497
Type I polyketide synthases (PKSs) are giant multidomain proteins that synthesize many therapeutics and other natural products. The synthesis proceeds by a thiotemplate mechanism whereby intermediates are covalently attached to the PKS. The release o
Autor:
Nicholas Brunet-Filion, Jeffrey W. Keillor, Kim Y.P. Apperley, Sara-Pier Piscopo, Élise De Francesco, Isabelle Roy, Catherine Hao, Vincent Saucier, Christophe Pardin
Publikováno v:
MedChemComm. 8(2)
Previous studies within our group have yielded a class of cinnamoyl-based competitive reversible inhibitors for tissue transglutaminase (TG2), with Ki values as low as 1.0 μM (compound CP4d). However, due to the electrophilic nature of their alkene
Autor:
Andrew Chen, Penny J. Le, Nader El Sayes, Jeffrey C. Smith, Kerkeslin Keillor, John C. Bell, Colin Davis, Christopher N. Boddy, Ramya Krishnan, Hwan Hee Son, Fabrice Le Boeuf, Jean-Simon Diallo, Andrew Macklin, Carlos R. Canez, Paula Ou, Christina Moi, Mark H. Dornan, Mohammed Selman, Christophe Pardin
Publikováno v:
Scientific Reports
The use of engineered viral strains such as gene therapy vectors and oncolytic viruses (OV) to selectively destroy cancer cells is poised to make a major impact in the clinic and revolutionize cancer therapy. In particular, several studies have shown
Autor:
Jeffrey W. Keillor, Pierre Thibault, William D. Lubell, Eric Bonneil, Roberto A. Chica, Joelle N. Pelletier, Isabelle Roy, Christophe Pardin
Publikováno v:
Biochemistry. 48:3346-3353
We have recently developed a new class of cinnamoyl derivatives as potent tissue transglutaminase (TG2) inhibitors. Herein, we report the synthesis of a diazirine derivative of these inhibitors and its application to the photolabeling of its binding