Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Emma Renard"'
Autor:
Isabella Attinger-Toller, Philipp Probst, Romain Bertrand, Emma Renard, Ramona Stark, Roger Santimaria, Dragan Grabulovski, Bernd Schlereth, Philipp Rene Spycher
Publikováno v:
Cancer Research. 83:LB221-LB221
The Araris site-specific and one-step peptide linker conjugation technology generates stable, safe and highly potent ADCs without the need for antibody engineering prior to payload conjugation. We generated an anti-Nectin-4 ADC that shows superior an
Autor:
Bernd Schlereth, Isabella Attinger-toller, Philipp Probst, Romain Bertrand, Ramona Stark, Roger Santimaria, Emma Renard, Rachael Fay, Jeff P. Sharman, Dragan Grabulovski, Philipp Spycher
Publikováno v:
Blood. 140:11568-11569
Autor:
Mélanie Guillemin, Pierre-Simon Bellaye, Franck Denat, Aurélie Prignon, Victor Goncalves, Emma Renard, Mathieu Moreau, Bertrand Collin
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2021, 64 (12), pp.8564-8578. ⟨10.1021/acs.jmedchem.1c00523⟩
Journal of Medicinal Chemistry, American Chemical Society, 2021, 64 (12), pp.8564-8578. ⟨10.1021/acs.jmedchem.1c00523⟩
Neurotensin receptor 1 (NTS1) is involved in the development and progression of numerous cancers, which makes it an interesting target for the development of diagnostic and therapeutic agents. A small molecule NTS1 antagonist, named [177Lu]Lu-IPN0108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b11600a1ea828363b7a3e1a659d0d687
https://hal.archives-ouvertes.fr/hal-03470823
https://hal.archives-ouvertes.fr/hal-03470823
Autor:
Emma, Renard, Mathieu, Moreau, Pierre-Simon, Bellaye, Mélanie, Guillemin, Bertrand, Collin, Aurélie, Prignon, Franck, Denat, Victor, Goncalves
Publikováno v:
Journal of medicinal chemistry. 64(12)
Neurotensin receptor 1 (NTS
Autor:
Emma Renard, Olivier Raguin, Victor Goncalves, Celine Mothes, Mathieu Moreau, Claire Bernhard, Peggy Provent, Frederic Boschetti, Franck Denat, Fabrice Viviani, Cyril Berthet
Publikováno v:
Cancer Research. 82:1401-1401
Molecular Radiotherapy (MRT) targeting SSTR2 or PSMA have proven to be highly efficient for the treatment of neuroendocrine or metastatic prostate cancer, respectively. Beyond the leading radiopharmaceutical molecules 177Lu-DOTATATE or 177Lu-PSMA-617
Autor:
Isabella Attinger-Toller, Philipp Probst, Romain Bertrand, Ramona Stark, Roger Santimaria, Emma Renard, Rachael Fay, Dragan Grabulovski, Bernd Schlereth, Philipp René Spycher
Publikováno v:
Cancer Research. 82:2910-2910
The Araris’ site-specific and 1-step linker conjugation technology aims at generating safe and highly potent ADCs without the need for antibody engineering prior to linker-payload conjugation. We developed a very stable anti-CD79b-MMAE ADC with thi
Autor:
Franck Denat, Martin Gotthardt, Emma Renard, Estel Collado Camps, Sanne A. M. van Lith, Annemarie Kip, Coline Canovas, Mark Rijpkema, Victor Goncalves
Publikováno v:
Cancers
Cancers, MDPI, 2021, 13 (3), pp.428. ⟨10.3390/cancers13030428⟩
Cancers, 13
Cancers, 13, 3
Cancers; Volume 13; Issue 3; Pages: 428
Cancers, Vol 13, Iss 428, p 428 (2021)
Cancers, MDPI, 2021, 13 (3), pp.428. ⟨10.3390/cancers13030428⟩
Cancers, 13
Cancers, 13, 3
Cancers; Volume 13; Issue 3; Pages: 428
Cancers, Vol 13, Iss 428, p 428 (2021)
Simple Summary Variable domains of heavy chain only antibodies are small proteins that can be used for tumor imaging and therapy upon conjugation of functional groups. As frequently used random conjugation techniques can decrease binding to the targe
Autor:
Emma Renard, Aurélie Prignon, Franck Denat, Pierre-Alix Dancer, Christophe Portal, Victor Goncalves
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2020, 63 (5), pp.2426-2433. ⟨10.1021/acs.jmedchem.9b01407⟩
Journal of Medicinal Chemistry, American Chemical Society, 2020, 63 (5), pp.2426-2433. ⟨10.1021/acs.jmedchem.9b01407⟩
International audience; Neurotensin receptor 1 (NTSR1) is overexpressed in most human pancreatic ductal adenocarcinomas. It makes it an attractive target for the development of pancreatic cancer imaging agents. In this study, we sought to develop a b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0244a6231604c84d06efca1566581aee
https://hal.archives-ouvertes.fr/hal-03470934
https://hal.archives-ouvertes.fr/hal-03470934
Publikováno v:
Nuclear Medicine and Biology. :S6-S7