Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Richard Charvet"'
Autor:
Grit Andersen, Grégory Meiffren, Susanne Famulla, Tim Heise, Aymeric Ranson, Cyril Seroussi, Rosy Eloy, Martin Gaudier, Richard Charvet, You‐Ping Chan, Olivier Soula, J. Hans DeVries
Publikováno v:
Diabetes, Obesity and Metabolism. 23
Autor:
Grégory Meiffren, Grit Andersen, J. Hans DeVries, Olivier Soula, Susanne Famulla, Richard Charvet, Martin Gaudier, Tim Heise, Aymeric Ranson, Rosy Eloy, You-Ping Chan, Cyril Seroussi
Publikováno v:
Diabetes, obesity & metabolism, 23(4), 961-970. Wiley-Blackwell
Aim: To compare the safety, pharmacokinetics and pharmacodynamics of ADO09 with insulin lispro (Lispro) and separate subcutaneous injections of human insulin and pramlintide (Ins&Pram) in 24 subjects with type 1 diabetes. Methods: At three dosing vis
Autor:
Martin Gaudier, Susanne Famulla, Cyril Seroussi, Rosy Eloy, Grégory Meiffren, Grit Andersen, Richard Charvet, Olivier Soula, Tim Heise, J. Hans DeVries, Aymeric Ranson, You-Ping Chan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53b092835fde852201dee76db3559eee
https://doi.org/10.1111/dom.14302/v2/response1
https://doi.org/10.1111/dom.14302/v2/response1
Autor:
J. Hans DeVries, Aymeric Ranson, Tim Heise, Martin Gaudier, Rémi Soula, Cyril Seroussi, Eric Zijlstra, Richard Charvet, Grégory Meiffren, Olivier Soula, Grit Andersen
Publikováno v:
Diabetes. 68
BCPramIns is developed to leverage the beneficial effects of PRAM on post-prandial BG control in a convenient co-formulation with INS. This double-blind, randomized cross-over study investigated pharmacodynamics, pharmacokinetics and safety of BCPram
Autor:
Grégory Meiffren, Olivier Soula, Aymeric Ranson, Yves Meyer, Bertrand Alluis, Richard Charvet, Rémi Soula, Charles Fortier, Alexandre Geissler
Publikováno v:
Diabetes. 67
Pramlintide (Symlin®) is currently used on top of mealtime insulin therapy by T1D or T2D patients to achieve a better control of post-prandial glucose excursion. Indeed, pramlintide affects the rate of postprandial glucose appearance by slowing down
Autor:
Katsuhiko Ariga, Jonathan P Hill, Michael V Lee, Ajayan Vinu, Richard Charvet and Somobrata Acharya
Publikováno v:
Science and Technology of Advanced Materials, Vol 9, Iss 1, p 014109 (2008)
The controlled fabrication of nanometer-scale objects is without doubt one of the central issues in current science and technology. However, existing fabrication techniques suffer from several disadvantages including size-restrictions and a general p
Externí odkaz:
https://doaj.org/article/7f5f541734fc4b36a09a6a39ac0a403b
Autor:
Akinori Saeki, Takuzo Aida, Yohei Yamamoto, Kenichi Kato, Masaki Takata, Shu Seki, Jungeun Kim, Richard Charvet, Takayuki Sasaki
Publikováno v:
Journal of the American Chemical Society. 134:2524-2527
Amphiphilic zinc porphyrin (P(Zn); electron donor, D)-fullerene (C(60); electron acceptor, A) dyads 2 and 3, bearing an identical hydrophilic wedge with triethylene glycol chains but different linkers between the P(Zn) and C(60) units, self-assemble
Publikováno v:
COSMOS. :141-171
The porphyrin macrocycle is one of the most frequently investigated functional molecular entities and can be incorporated into advanced functional nanomaterials upon formation of organized nanostructures. Thus, study of the science and technology of
Autor:
Ajayan Vinu, Jonathan P. Hill, Katsuhiko Ariga, Somobrata Acharya, Richard Charvet, Atsuomi Shundo
Publikováno v:
Advanced Science Letters. 1:28-58
New phenomena, properties, and functions contributing to advanced sciences can be discovered, examined, and developed in nanospaces. Sophisticated design of molecular hosts and their assemblies can provide excellent nanospaces with predictable proper
Autor:
Yasuyuki Araki, Richard Charvet, Jonathan P. Hill, Francis D'Souza, Atula S. D. Sandanayaka, Katsuhiko Ariga, Amy L. McCarty, Paul A. Karr, Osamu Ito, Melvin E. Zandler
Publikováno v:
European Journal of Organic Chemistry. 2006:595-603
The first example of a porphyrin-quinonoid donor–acceptor triad featuring (tetraphenylporphinato)zinc(II) moieties covalently attached to an oxoporphyrinogen through its macrocyclic nitrogen atoms is reported. This arrangement of chromophores resul