Zobrazeno 1 - 10
of 1 960
pro vyhledávání: '"proteïnes"'
Publikováno v:
In Médecine des maladies métaboliques December 2024 18(8):674-679
Autor:
Fafournoux, Pierre
Publikováno v:
In Médecine des maladies métaboliques December 2024 18(8):664-673
Autor:
Gaudichon, Claire, Benhaddou, Soukaïna
Publikováno v:
In Médecine des maladies métaboliques December 2024 18(8):648-655
Publikováno v:
In Médecine des maladies métaboliques December 2024 18(8):680-687
Autor:
Bompart, Catherine, Gueugneau, Marine
Publikováno v:
In Médecine des maladies métaboliques December 2024 18(8):656-663
Publikováno v:
Oncotarget. 14:503-513
The signaling pathways displayed by cancer cells are often composed by the same components than the physiological ones, yet the overall result is a pathological deregulation. The non-receptor protein tyrosine kinase Src is a good example. Src is the
Autor:
Ruben A. Mesa, Stacie Hudgens, Lysbeth Floden, Claire N. Harrison, Jeanne Palmer, Vikas Gupta, Donal P. McLornan, Mary F. McMullin, Jean‐Jaques Kiladjian, Lynda Foltz, Uwe Platzbecker, M. Laura Fox, Adam J. Mead, David M. Ross, Stephen T. Oh, Andrew Perkins, Michael F. Leahy, Samineh Deheshi, Rafe Donahue, Barbara J. Klencke, Srdan Verstovsek
Publikováno v:
Mesa, R A, Hudgens, S, Floden, L, Harrison, C N, Palmer, J, Gupta, V, McLornan, D P, McMullin, M F, Kiladjian, J-J, Foltz, L, Platzbecker, U, Fox, M L, Mead, A J, Ross, D M, Oh, S T, Perkins, A, Leahy, M F, Deheshi, S, Donahue, R, Klencke, B J & Verstovsek, S 2023, ' Symptomatic benefit of momelotinib in patients with myelofibrosis: results from the SIMPLIFY phase III studies ', Cancer Medicine . https://doi.org/10.1002/cam4.5799
Scientia
Scientia
Momelotinib; Myelofibrosis; Patient-reported outcomes Momelotinib; Mielofibrosi; Resultats informats pel pacient Momelotinib; Mielofibrosis; Resultados informados por el paciente Background Myelofibrosis (MF)-associated constitutional symptoms can se
Autor:
Laura Rey-Barroso, Mónica Roldán, Francisco J Burgos-Fernández, Ignacio Isola, Anna Ruiz Llobet, Susanna Gassiot, Edurne Sarrate, Meritxell Vilaseca
Publikováno v:
Microscopy and Microanalysis. 29:777-785
In hereditary spherocytosis (HS), genetic mutations in the cell membrane and cytoskeleton proteins cause structural defects in red blood cells (RBCs). As a result, cells are rigid and misshapen, usually with a characteristic spherical form (spherocyt
Autor:
Ramón Diez-Feijóo, Concepción Fernández-Rodríguez, Marta Lafuente, Nieves García-Gisbert, Ana Ferrer, Luis Colomo, Marta Salido, Antonio Salar
Publikováno v:
Blood Advances. 7:162-166
Publikováno v:
Free Radical Biology and Medicine. 192:63-76
Selenophosphate synthetases use selenium and ATP to synthesize selenophosphate. This is required for biological utilization of selenium, most notably for the synthesis of the non-canonical amino acid selenocysteine (Sec). Therefore, selenophosphate s