Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Itedale Namro Redwan"'
Autor:
Christian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko, Pierre‐Alexandre Laurent, Giulia Della Rosa, Claudia Del Fante, Damian Edward Dalle Nogare, Florian Jug, Cesare Perotti, Koji Eto, Alessandro Pecci, Itedale Namro Redwan, Alessandra Balduini
Publikováno v:
Advanced Science, Vol 11, Iss 18, Pp n/a-n/a (2024)
Abstract Hematopoietic stem and progenitor cells (HSPCs) continuously generate platelets throughout one's life. Inherited Platelet Disorders affect ≈ 3 million individuals worldwide and are characterized by defects in platelet formation or function
Externí odkaz:
https://doaj.org/article/0fb9676f26ca4a47a63e8f2889c371c5
Autor:
Lukas Zeger, Povilas Barasa, Yilin Han, Josefin Hellgren, Itedale Namro Redwan, Myrthe E. Reiche, Gunnar Florin, Gustaf Christoffersson, Elena N. Kozlova
Publikováno v:
Cells, Vol 13, Iss 18, p 1588 (2024)
We previously demonstrated that boundary cap neural crest stem cells (BCs) induce the proliferation of beta-cells in vitro, increase survival of pancreatic islets (PIs) in vivo after transplantation, and themselves strongly increase their proliferati
Externí odkaz:
https://doaj.org/article/636aaf40a1b54e409755972492c18a08
Autor:
Francesca Vittoria Sbrana, Riccardo Pinos, Federica Barbaglio, Davide Ribezzi, Fiorella Scagnoli, Lydia Scarfò, Itedale Namro Redwan, Hector Martinez, Silvia Farè, Paolo Ghia, Cristina Scielzo
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Chronic Lymphocytic Leukemia (CLL) represents the most common leukemia in the western world and remains incurable. Leukemic cells organize and interact in the lymphoid tissues, however what actually occurs in these sites has not been fully elucidated
Externí odkaz:
https://doaj.org/article/71214914a56943d29e9a5805b1f4366d
Publikováno v:
Molecules, Vol 14, Iss 12, Pp 5124-5143 (2009)
A versatile method for the synthesis of chiral 1,4-disubstituted-1,2,3-triazole derivatives starting from easily accessible naturally occurring D-or L-amino acids as chiral synthons is described. The amino acids were converted into azido alcohols, fo
Externí odkaz:
https://doaj.org/article/4368f4b501f943ef9102215eab2b0dfc
Autor:
Flavio L. Ronzoni, Flaminia Aliberti, Franca Scocozza, Laura Benedetti, Ferdinando Auricchio, Maurilio Sampaolesi, Gabriella Cusella, Itedale Namro Redwan, Gabriele Ceccarelli, Michele Conti
Publikováno v:
Journal of tissue engineering and regenerative medicine. 16(5)
Skeletal muscle regeneration is one of the major areas of interest in sport medicine as well as trauma centers. Three-dimensional (3D) bioprinting (BioP) is nowadays widely adopted to manufacture 3D constructs for regenerative medicine but a comparis
Autor:
Itedale Namro Redwan, Laure Voisin, Carlos Solano, David Bliman, Sylvain Meloche, Christine Dyrager, Guillermo Fernández de Trocóniz, Morten Grøtli
Publikováno v:
European Journal of Medicinal Chemistry. 85:127-138
Inhibition or allosteric modulation of mitogen-activated protein kinase kinases MEK1 and MEK2 (MEK1/2) represent a promising strategy for the discovery of new specific anticancer agents. In this paper, structure-based design, beginning from the lead
Autor:
Hanna Jacobson Ingemyr, Christopher P. Lawson, Thomas Ljungdahl, Itedale Namro Redwan, Morten Grøtli
Publikováno v:
European Journal of Organic Chemistry. 2012:3665-3669
The solid-phase synthesis of 5'-O-[N-(acyl)sulfamoyl]adenosine derivatives is described. The use of a Rink amide polystyrene solid support together with an appropriately protected ribo-purine starting material allowed for the development of a highly
Publikováno v:
Tetrahedron. 68:1507-1514
Aminoacyl-tRNA synthetases (aaRSs) constitute a family of enzymes that transfer amino acids to their corresponding tRNA molecules to form aminoacyl-tRNAs and have been validated as potential drug targets. Sulfamoyloxy-linked aminoacyl-AMP analogues a
Publikováno v:
Molecules
Volume 14
Issue 12
Pages 5124-5143
Molecules, Vol 14, Iss 12, Pp 5124-5143 (2009)
Volume 14
Issue 12
Pages 5124-5143
Molecules, Vol 14, Iss 12, Pp 5124-5143 (2009)
A versatile method for the synthesis of chiral 1,4-disubstituted-1,2,3-triazole derivatives starting from easily accessible naturally occurring D-or L-amino acids as chiral synthons is described. The amino acids were converted into azido alcohols, fo
Publikováno v:
ChemInform. 45