Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gaël Palais"'
Autor:
Hima Priyanka Nadimpalli, Georgia Katsioudi, Enes Salih Arpa, Lies Chikhaoui, Alaaddin Bulak Arpat, Angelica Liechti, Gaël Palais, Claudia Tessmer, Ilse Hofmann, Bruno Galy, David Gatfield
Publikováno v:
Genome Biology, Vol 25, Iss 1, Pp 1-28 (2024)
Abstract Background Cellular iron homeostasis is regulated by iron regulatory proteins (IRP1 and IRP2) that sense iron levels (and other metabolic cues) and modulate mRNA translation or stability via interaction with iron regulatory elements (IREs).
Externí odkaz:
https://doaj.org/article/adbd80f2d6ec4f649e63fe30ae6f1eef
Autor:
Maria Qatato, Michael Bonadonna, Gaël Palais, Alina Ertl, Gabriele Schmidt, Maria Polycarpou-Schwarz, Zoubida Karim, Bruno Galy
Publikováno v:
HemaSphere, Vol 6, Iss 3, p e693 (2022)
Externí odkaz:
https://doaj.org/article/856c9223e7c740bfa25f36d4169ac7b6
Autor:
Kristofer Bodvard, Ken Peeters, Friederike Roger, Natalie Romanov, Aeid Igbaria, Niek Welkenhuysen, Gaël Palais, Wolfgang Reiter, Michel B. Toledano, Mikael Käll, Mikael Molin
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-11 (2017)
While yeasts lack dedicated photoreceptors, they nonetheless possess metabolic rhythms responsive to light. Here the authors find that light signalling in budding yeast involves the production of H2O2, which in turn regulates protein kinase A through
Externí odkaz:
https://doaj.org/article/6ed3152d028e43cd993b4e225ebf7661
Autor:
Maria, Qatato, Michael, Bonadonna, Gaël, Palais, Alina, Ertl, Gabriele, Schmidt, Maria, Polycarpou-Schwarz, Zoubida, Karim, Bruno, Galy
Publikováno v:
HemaSphere. 6(3)
Autor:
Claudine Deloménie, Rajagopal Krishnamoorthy, Jean-Marie Dupret, Dominique Droz, Claudine Junien, Natacha Martin, Raymonde Bouvier, Catherine Gallou, Stéphane Martinet, Gaël Palais, Arnaud Mejean, Christophe Béroud, Sandrine Longuemaux
Publikováno v:
Pharmacogenetics. 11(6)
The von Hippel-Lindau (VHL) tumour suppressor gene is commonly mutated in renal cell carcinoma of clear cell type (CCRCC). We investigated the possible relationship between VHL mutations in sporadic CCRCC and polymorphism of genes encoding enzymes in
Autor:
Elisabeth Tybl, Hiromi Gunshin, Sanjay Gupta, Tomasa Barrientos, Michael Bonadonna, Ferran Celma Nos, Gael Palais, Zoubida Karim, Mayka Sanchez, Nancy C. Andrews, Bruno Galy
Publikováno v:
HemaSphere, Vol 4, Iss 5, p e459 (2020)
Externí odkaz:
https://doaj.org/article/9d7dc065e58e45ee9233bc35b0728807