Zobrazeno 1 - 3
of 3
pro vyhledávání: '"MESH: Kinetin"'
Autor:
Petr Džubák, Tibor Béres, Percy Niemann, Miroslav Strnad, Karel Doležal, Marian Hajduch, Jiří Voller, Pierre Alexandre Kaminski, Marek Zatloukal
Publikováno v:
Phytochemistry
Phytochemistry, 2017, 136, pp.156-164. ⟨10.1016/j.phytochem.2017.01.004⟩
Phytochemistry, 2017, 136, pp.156-164. ⟨10.1016/j.phytochem.2017.01.004⟩
International audience; Cytokinin ribosides (N6-substituted adenosines) have demonstrated anticancer activity in various cultured cell lines, several xenografts and even a small clinical trial. Effects of kinetin riboside, N6-benzyladenosine (BAR) an
Autor:
Mario Noti, Dominic Leiser, Atanas G. Atanasov, Kristina Schoonjans, Nadia Corazza, Corinne Roesselet, Thomas Brunner
Publikováno v:
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2008, 22 (12), pp.4117-25. ⟨10.1096/fj.08-114157⟩
FASEB Journal, 2008, 22 (12), pp.4117-25. ⟨10.1096/fj.08-114157⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2008, 22 (12), pp.4117-25. ⟨10.1096/fj.08-114157⟩
FASEB Journal, 2008, 22 (12), pp.4117-25. ⟨10.1096/fj.08-114157⟩
International audience; Glucocorticoids are anti-inflammatory steroids with important applications in the treatment of inflammatory diseases. Endogenous glucocorticoids are mainly produced by the adrenal glands, although there is increasing evidence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::071f5992861bd5cbe6e4d26c383f2215
https://www.hal.inserm.fr/inserm-00350850
https://www.hal.inserm.fr/inserm-00350850
Autor:
Sandra Gill, Conxi Lázaro, Lijuan Liu, Robin Reed, El Chérif Ibrahim, Matthew M. Hims, Ranjit S. Shetty, James F. Gusella, Maire Leyne, James Mull, Susan A. Slaugenhaupt
Publikováno v:
Journal of Molecular Medicine
Journal of Molecular Medicine, 2007, 85 (2), pp.149-61. ⟨10.1007/s00109-006-0137-2⟩
Journal of Molecular Medicine, 2007, 85 (2), pp.149-61. ⟨10.1007/s00109-006-0137-2⟩
Mutations that affect the splicing of pre-mRNA are a major cause of human disease. Familial dysautonomia (FD) is a recessive neurodegenerative disease caused by a T to C transition at base pair 6 of IKBKAP intron 20. This mutation results in variable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44cc5b1fd308cecb6a429a65ea3af9d6
https://hal.science/hal-00320234
https://hal.science/hal-00320234